Oryctolagus cuniculus (rabbit): 100009030 Help Entry 100009030         CDS       T03373                                  Gene name WNT11, WNT-11 Definition (RefSeq) Wnt family member 11   KO K01384   wingless-type MMTV integration site family, member 11 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100009030 (WNT11)    04390 Hippo signaling pathway     100009030 (WNT11)    04150 mTOR signaling pathway     100009030 (WNT11)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100009030 (WNT11)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100009030 (WNT11)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100009030 (WNT11)    05205 Proteoglycans in cancer     100009030 (WNT11)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100009030 (WNT11)    05226 Gastric cancer     100009030 (WNT11)    05217 Basal cell carcinoma     100009030 (WNT11)    05224 Breast cancer     100009030 (WNT11)   09164 Neurodegenerative disease    05010 Alzheimer disease     100009030 (WNT11)    05022 Pathways of neurodegeneration - multiple diseases     100009030 (WNT11)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100009030 (WNT11)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100009030 (WNT11)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100009030 (WNT11) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100009030 (WNT11) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100009030 NCBI-ProteinID:  NP_001075693 Ensembl:  ENSOCUG00000001726 UniProt:  Q27Q51 LinkDB All DBs Position 1 AA seq 354 aa AA seqDB search MRARPQVCEALLFALALHTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR SNLELMHTIVRAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK TGSQANKLMRLHNSEVGRQALRASLEVKCKCHGVSGSCSIRTCWKGLQELRDVAADLKSR YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERAVERYVCK NT seq 1065 nt NT seq  +upstreamnt  +downstreamnt atgagggcgcggccgcaggtctgcgaggctctgctcttcgccctggcgctacacaccggc gtgtgctatggcatcaagtggctggcgctgtccaagacgccggcggccttggcactgaac cagacgcagcactgcaagcagctggagggcctggtgtccgcgcaggtgcagctgtgccgc agcaacctggagctcatgcacaccatcgtgcgcgccgcccgcgaggtcatgaaggcctgc cgcagggccttcgccgacatgcgctggaactgctcctccatcgagctcgcccccaactac ctgctcgacctggagagagggacccgggagtcggccttcgtgtatgcgctgtcggcggct gccatcagccacgccatcgcccgggcctgcacctctggcgacctgcccggctgctcctgc ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct ctgcgtgcctctctggaagtgaagtgtaagtgccacggggtgtcgggctcctgctccatc cgcacctgctggaaggggctgcaggagctgcgggatgtggccgctgacctcaagagccgc tacctgtcggccaccaaggtggtgcacagacccatgggcacccgcaagcacctggtgccc aaggacctggacatccggcccgtgaaggactcggagctcgtgtacctgcagagctcgccc gacttctgcatgaagaacgagaaggtgggctcccacgggacccaggacaggcagtgcaac aagacgtcgaatggcagcgacagctgtgacctcatgtgctgtgggcgcggctacaacccc tacacggaccgcgtggtggagcggtgccactgcaagtaccactggtgctgctacgtgacg tgccgccgctgtgagcgcgccgtggagcgctatgtctgcaagtga

Oryctolagus cuniculus (rabbit): 100009033 Help Entry 100009033         CDS       T03373                                  Gene name WNT3 Definition (RefSeq) Wnt family member 3   KO K00312   wingless-type MMTV integration site family, member 3 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05206   MicroRNAs in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100009033 (WNT3)    04390 Hippo signaling pathway     100009033 (WNT3)    04150 mTOR signaling pathway     100009033 (WNT3)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100009033 (WNT3)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100009033 (WNT3)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100009033 (WNT3)    05206 MicroRNAs in cancer     100009033 (WNT3)    05205 Proteoglycans in cancer     100009033 (WNT3)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100009033 (WNT3)    05226 Gastric cancer     100009033 (WNT3)    05217 Basal cell carcinoma     100009033 (WNT3)    05224 Breast cancer     100009033 (WNT3)   09164 Neurodegenerative disease    05010 Alzheimer disease     100009033 (WNT3)    05022 Pathways of neurodegeneration - multiple diseases     100009033 (WNT3)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100009033 (WNT3)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100009033 (WNT3)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100009033 (WNT3) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100009033 (WNT3) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100009033 NCBI-ProteinID:  XP_002719498 Ensembl:  ENSOCUG00000014805 UniProt:  G1T851 LinkDB All DBs Position 19 AA seq 355 aa AA seqDB search MEPHLLRLLLGLLLGGTRALAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS ASEMVVEKHRESRGWVETLRAKYALFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC NITSHGIDGCDLLCCGRGHNTRTEKRKEKCHCVFHWCCYVSCQECIRIYDVHTCK NT seq 1068 nt NT seq  +upstreamnt  +downstreamnt atggagccccacctgctccggctgctcctcggcctgctgctcggtggcaccagggccctc gccggctacccaatttggtggtccctggccctgggccagcagtacacatctctgggctcc cagcccctgctctgcggctccatcccaggcctggtccccaagcagctgcgcttctgccgc aactacatcgagatcatgcccagcgtggccgagggcgtgaagctgggcatccaggagtgc cagcaccagttccggggccgccgctggaactgcaccaccatagacgacagcctggccatc ttcgggcccgtcctggacaaagccacccgggagtcggccttcgtgcacgccatcgcctcg gccggcgtggccttcgccgtcacgcgctcctgcgccgagggcacctccaccatctgtggc tgcgactctcatcacaaggggccgcccggcgaaggctggaagtggggcggctgcagcgaa gacgccgacttcggggtgctggtgtcccgcgagttcgctgacgcccgcgagaaccggccg gatgcccgctcggccatgaacaagcacaacaacgaggcgggccgcacgaccatcctggac cacatgcacctcaagtgcaagtgccacgggctgtcgggcagctgcgaggtgaagacctgc tggtgggcccagcccgacttccgtgccatcggcgacttcctcaaggacaagtacgacagc gcctcggagatggtggtggagaagcaccgggagtcccggggctgggtggagaccctgcgc gccaagtacgcgctcttcaagccgcccaccgagagggacctggtctactatgagaactcc cccaacttctgcgagcccaacccagagacgggctcctttggcaccagggaccggacttgc aacatcacctcccacggcattgacggctgcgacctgctgtgctgtggccgcggccacaac acgaggacggagaagaggaaggagaagtgccactgcgtcttccactggtgctgctacgtc agctgccaggagtgcatccgcatctacgacgtgcacacctgcaagtag

Oryctolagus cuniculus (rabbit): 100009381 Help Entry 100009381         CDS       T03373                                  Gene name WNT5A, WNT-5A Definition (RefSeq) Wnt family member 5A   KO K00444   wingless-type MMTV integration site family, member 5 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04360   Axon guidance ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100009381 (WNT5A)    04390 Hippo signaling pathway     100009381 (WNT5A)    04150 mTOR signaling pathway     100009381 (WNT5A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100009381 (WNT5A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100009381 (WNT5A)   09158 Development and regeneration    04360 Axon guidance     100009381 (WNT5A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100009381 (WNT5A)    05205 Proteoglycans in cancer     100009381 (WNT5A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100009381 (WNT5A)    05226 Gastric cancer     100009381 (WNT5A)    05217 Basal cell carcinoma     100009381 (WNT5A)    05224 Breast cancer     100009381 (WNT5A)   09164 Neurodegenerative disease    05010 Alzheimer disease     100009381 (WNT5A)    05022 Pathways of neurodegeneration - multiple diseases     100009381 (WNT5A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100009381 (WNT5A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100009381 (WNT5A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100009381 (WNT5A) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100009381 (WNT5A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100009381 NCBI-ProteinID:  NP_001076134 Ensembl:  ENSOCUG00000000380 UniProt:  Q27Q52 LinkDB All DBs Position 9 AA seq 380 aa AA seqDB search MKKSIGILSPGVALGTAGSAMSSKFFVMALAVFFSFAQVVIEANSWWSLGMNNPVQMSEV YIIGAQPLCSQLAGLSQGQKKLCHLYQDHMQYIGEGAKTGIKECQYQFRHRRWNCSTVDN TSVFGRVMQIGSRETAFTYAVSAAGVVNAMSRACREGELSTCGCSRAARPKDLPRDWLWG GCGDNIDYGYRFAKEFVDARERERIHAKGSYESARILMNLHNNEAGRRTVYNLADVACKC HGVSGSCSLKTCWLQLADFRKVGDALKEKYDSAAAMRLNSRGKLVQVNSRFNSPTTQDLV YIDPSPDYCVRNESTGSLGTQGRLCNKTSEGMDGCELMCCGRGYDQFKTVQTERCHCKFH WCCYVKCKKCTEIVDQFVCK NT seq 1143 nt NT seq  +upstreamnt  +downstreamnt atgaagaagtccattggcatattaagcccaggcgttgctttggggactgctggaagtgca atgtcttccaagttcttcgtaatggctttggccgtatttttttccttcgcccaggttgta atagaagccaattcttggtggtccctaggtatgaataaccctgttcagatgtcagaagta tacatcataggagcgcagcctctctgcagccaactggcgggactttctcaaggacagaag aaactgtgccacttgtatcaggaccacatgcagtacatcggggaaggcgcgaagaccggc atcaaagaatgccagtatcagttccgacatcgaaggtggaactgcagcactgtggataac acgtccgtcttcggcagagtgatgcagataggcagccgcgagacggccttcacgtacgct gtgagcgccgcaggggtggtgaacgccatgagccgggcgtgccgggagggcgagctgtcc acctgcggctgcagccgggcggcgcgccccaaagacctgccgcgggactggctctggggc ggctgcggcgacaacatcgactacggataccgcttcgccaaggagtttgtggacgcacgc gagcgggagcgcatccacgccaagggctcctatgagagcgcgcgcatcctcatgaacctg cacaacaacgaggccggccgcaggacggtgtacaacctggccgatgtggcctgcaagtgc cacggagtatccggctcgtgtagcctcaagacgtgctggctgcagctggcggacttccgc aaggtgggcgacgcgctcaaggagaaatacgacagcgcggccgccatgcggctcaacagc cggggcaagctggtgcaggtcaacagccgcttcaactcgcccaccacgcaggacctggtc tacatcgaccccagccccgactactgtgtgcgcaacgagagcacgggctcgctgggcacc cagggccgcctgtgcaacaagacgtccgagggcatggacggctgtgagcttatgtgctgc ggccgcggctacgaccagttcaagacggtacagacagagcgctgccactgcaagttccac tggtgctgctatgtcaagtgcaagaagtgcacggagatcgtggaccagtttgtgtgcaag tag

Oryctolagus cuniculus (rabbit): 100126569 Help Entry 100126569         CDS       T03373                                  Gene name WNT2 Definition (RefSeq) Wnt family member 2   KO K00182   wingless-type MMTV integration site family, member 2 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100126569 (WNT2)    04390 Hippo signaling pathway     100126569 (WNT2)    04150 mTOR signaling pathway     100126569 (WNT2)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100126569 (WNT2)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100126569 (WNT2)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100126569 (WNT2)    05205 Proteoglycans in cancer     100126569 (WNT2)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100126569 (WNT2)    05226 Gastric cancer     100126569 (WNT2)    05217 Basal cell carcinoma     100126569 (WNT2)    05224 Breast cancer     100126569 (WNT2)   09164 Neurodegenerative disease    05010 Alzheimer disease     100126569 (WNT2)    05022 Pathways of neurodegeneration - multiple diseases     100126569 (WNT2)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100126569 (WNT2)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100126569 (WNT2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100126569 (WNT2) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100126569 (WNT2) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100126569 NCBI-ProteinID:  NP_001164513 Ensembl:  ENSOCUG00000016173 UniProt:  Q09YN1 LinkDB All DBs Position 7 AA seq 360 aa AA seqDB search MNAPLGGIWLGLPLLLTWLSPEVSSSWWYMRATGDSSRVMCDNVPGLVSRQRQLCHRHPD VMRAIGLGVAEWTAECQYQFRQHRWNCNTLDRDHGLFGRVLLRSSRESAFVYAISSAGVV FAITRACSQGELKSCSCDPKKKGTAKDSKGTFDWGGCSDNIDYGIKFARAFVDAKERKGK DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG AIQVVMNQDGTGFTVANKRFKKPTKNDLVYFENSPDYCIRDREAGSPGTAGRVCNLTSRG MDSCEVMCCGRGYDTSRVTRMTKCECKFHWCCAVRCQDCLEALDVHTCKAPKSADWTTPT NT seq 1083 nt NT seq  +upstreamnt  +downstreamnt atgaacgcccctctcggtggaatctggctggggctccctctgctcttgacctggctcagc cccgaggtcagctcttcatggtggtacatgagagctacaggtgactcctccagggtgatg tgtgacaatgtgccaggcctggtgagccgccagcggcagctgtgccaccgacacccggac gtgatgcgtgccataggcctgggtgtggccgagtggacagcagagtgccagtatcagttc cgacagcaccgctggaactgcaacaccctggacagggatcacggcctctttggcagggtt ctgctccgaagtagtcgggaatctgcctttgtatacgccatctcctcagctggagttgta tttgccatcaccagggcctgtagccaaggagaattaaaatcctgttcctgtgatccaaag aagaaaggaactgccaaggacagcaagggcaccttcgactggggtggctgcagtgataac attgactatgggatcaagtttgcccgagcctttgtggatgccaaggaaaggaaaggaaag gatgccagagcgctgatgaatcttcacaacaacagagcgggcaggaaggctgtaaagcgg ttcttgaaacaagagtgcaagtgccacggtgtgagcggctcgtgtactctgcggacgtgc tggctggccatggccgacttcaggaaaacgggcgattacctctggaggaagtacaatgga gccatccaggtcgtcatgaaccaggatggcactggtttcactgtggctaacaagaggttt aagaagccaacgaaaaatgaccttgtgtactttgagaattctccagactactgtatcagg gaccgagaggcaggctccccgggtacagcaggtcgtgtgtgcaacctgacgtccagaggc atggacagctgtgaagtcatgtgctgcgggagaggctacgacacctcccgcgtcacccgg atgaccaagtgcgagtgtaagttccactggtgctgtgccgtgcgttgccaggactgcctg gaggccctggacgtgcacacatgcaaggctcccaagagtgctgactggacaaccccaaca tga

Oryctolagus cuniculus (rabbit): 100303773 Help Entry 100303773         CDS       T03373                                  Gene name WNT4 Definition (RefSeq) Wnt family member 4   KO K00408   wingless-type MMTV integration site family, member 4 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04360   Axon guidance ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04919   Thyroid hormone signaling pathway ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100303773 (WNT4)    04390 Hippo signaling pathway     100303773 (WNT4)    04150 mTOR signaling pathway     100303773 (WNT4)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100303773 (WNT4)  09150 Organismal Systems   09152 Endocrine system    04919 Thyroid hormone signaling pathway     100303773 (WNT4)    04916 Melanogenesis     100303773 (WNT4)   09158 Development and regeneration    04360 Axon guidance     100303773 (WNT4)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100303773 (WNT4)    05205 Proteoglycans in cancer     100303773 (WNT4)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100303773 (WNT4)    05226 Gastric cancer     100303773 (WNT4)    05217 Basal cell carcinoma     100303773 (WNT4)    05224 Breast cancer     100303773 (WNT4)   09164 Neurodegenerative disease    05010 Alzheimer disease     100303773 (WNT4)    05022 Pathways of neurodegeneration - multiple diseases     100303773 (WNT4)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100303773 (WNT4)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100303773 (WNT4)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100303773 (WNT4) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100303773 (WNT4) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100303773 NCBI-ProteinID:  XP_008263935 Ensembl:  ENSOCUG00000022473 LinkDB All DBs Position 13 AA seq 296 aa AA seqDB search MCKRNLEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAV SSAGVAFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRER SKGASSSRALMNLHNNEAGRKAILSHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALK EKFDGATEVEPRRVGSSRALVPRNGAVQPQTDEDLGYLEPSPDFCEQDLRSGVLGTRGRT CNKTSKAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR NT seq 891 nt NT seq  +upstreamnt  +downstreamnt atgtgcaagcgcaacctggaggtgatggactcggtgcgccgcggcgcgcagctggccatc gaggagtgccagtaccagttccggaaccggcgctggaactgctccacgctcgactccctg cccgtcttcggcaaggtggtgacgcaagggactcgggaggcggccttcgtgtacgcagtc tcctctgcaggggtggccttcgcggtgacacgggcgtgcagcagcggggagctggagaag tgcggctgtgaccgcacggtgcacggggtcagcccccagggcttccagtggtcgggatgc tcggacaacatcgcctacggcgtggccttctcgcagtccttcgtggacgtgcgggagagg agcaagggtgcctcgtccagccgggcgctcatgaacctccataacaacgaggccggcaga aaggccatcctgtcacacatgcgggtggagtgcaagtgccacggggtgtcgggctcctgc gaggtgaagacgtgctggcgggcggtgccgcccttccgccaggtgggccacgcgctgaag gagaagttcgacggcgccaccgaggtggagccacgccgggtgggctcctccagggccctg gtgccgcgcaacggggcagttcaaccgcaaacggacgaggacctggggtacctggagccc agcccggacttctgcgagcaggacttacgcagcggcgtgctgggcacgaggggccgcacc tgcaacaagacgtccaaggccatcgacggctgcgagctgctgtgctgcggccgcggcttc cacacggcgcaggtggagctggcggaacgctgcagctgcaaattccactggtgctgcttc gtcaagtgccgccagtgccagcggctggtggagctgcacacgtgccggtga

Oryctolagus cuniculus (rabbit): 100342870 Help Entry 100342870         CDS       T03373                                  Gene name WNT8A Definition (RefSeq) Wnt family member 8A   KO K00714   wingless-type MMTV integration site family, member 8 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100342870 (WNT8A)    04390 Hippo signaling pathway     100342870 (WNT8A)    04150 mTOR signaling pathway     100342870 (WNT8A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100342870 (WNT8A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100342870 (WNT8A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100342870 (WNT8A)    05205 Proteoglycans in cancer     100342870 (WNT8A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100342870 (WNT8A)    05226 Gastric cancer     100342870 (WNT8A)    05217 Basal cell carcinoma     100342870 (WNT8A)    05224 Breast cancer     100342870 (WNT8A)   09164 Neurodegenerative disease    05010 Alzheimer disease     100342870 (WNT8A)    05022 Pathways of neurodegeneration - multiple diseases     100342870 (WNT8A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100342870 (WNT8A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100342870 (WNT8A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100342870 (WNT8A) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100342870 (WNT8A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100342870 NCBI-ProteinID:  XP_002710155 Ensembl:  ENSOCUG00000005191 UniProt:  G1SNE4 LinkDB All DBs Position 3 AA seq 352 aa AA seqDB search MGDLVLLWVAVGMCSATFRASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMHTITKNCSMGDFENCGCDESKNG KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVKATMRRTC KCHGISGSCSIQTCWLQLADFREMGDYLKAKYDRALKIEMDKRRLRAGNSAEGHWAPTEA FLPSAEAELVFLEESPDYCTRNSSLGVQGTEGRECLQHSHNTSRRERRSCGRLCSECGLQ VEERRTEATSSCNCKFHWCCTVKCDQCRHVVNRYYCTRSPGTAQSWAKGSAW NT seq 1059 nt NT seq  +upstreamnt  +downstreamnt atgggagacctcgttctgctctgggtggctgtgggcatgtgcagtgccaccttccgtgcc tctgcctggtcagtgaacaatttcctgataactggccctaaggcctacctgacctatact accagcgtggccttgggggcccagagcggcattgaggagtgtaagttccagtttgcttgg gaacgttggaactgcccggaaaatgctctccagctctccacccacaacaggctgagaagc gccaccagagagacttccttcattcatgccatcagctcagctggagtcatgcacactatc accaagaactgcagcatgggcgactttgaaaactgtggctgcgatgagtcaaaaaacggg aaaacaggaggccatggctggatctggggaggctgcagcgacaatgtggaatttggggaa aggatctccaaactctttgtggacagtttggagaaggggaaggatgccagagccctgatg aatctccacaacaacagggccggcaggctggcagtgaaagccaccatgagaaggacctgc aagtgtcacggcatctcggggagctgcagcatccagacctgctggttgcagctggctgac ttccgggagatgggcgactacctgaaggccaagtacgaccgggcgctgaaaatcgagatg gacaagcggcggctaagagctgggaacagcgccgagggccactgggcgcccacagaggcc tttcttcctagtgcagaggccgagctggtctttctagaggagtcgccagattactgcacc cgcaattccagcctgggcgtccagggcactgagggccgtgagtgcctgcagcacagccac aacacctcccggagggagcgacgcagctgcgggcgcctgtgctccgagtgtgggctgcag gtggaagagaggcgaaccgaggccaccagcagctgtaactgcaaattccactggtgctgc acggtcaagtgtgaccagtgtaggcatgtggtgaacagatactactgcacccgctcccca ggcacggcccagtcctgggctaagggcagtgcctggtaa

Oryctolagus cuniculus (rabbit): 100348986 Help Entry 100348986         CDS       T03373                                  Gene name WNT6 Definition (RefSeq) Wnt family member 6   KO K00445   wingless-type MMTV integration site family, member 6 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100348986 (WNT6)    04390 Hippo signaling pathway     100348986 (WNT6)    04150 mTOR signaling pathway     100348986 (WNT6)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100348986 (WNT6)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100348986 (WNT6)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100348986 (WNT6)    05205 Proteoglycans in cancer     100348986 (WNT6)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100348986 (WNT6)    05226 Gastric cancer     100348986 (WNT6)    05217 Basal cell carcinoma     100348986 (WNT6)    05224 Breast cancer     100348986 (WNT6)   09164 Neurodegenerative disease    05010 Alzheimer disease     100348986 (WNT6)    05022 Pathways of neurodegeneration - multiple diseases     100348986 (WNT6)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100348986 (WNT6)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100348986 (WNT6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100348986 (WNT6) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100348986 (WNT6) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Collagen Motif Other DBs NCBI-GeneID:  100348986 NCBI-ProteinID:  XP_008257392 Ensembl:  ENSOCUG00000024007 LinkDB All DBs Position 7 AA seq 365 aa AA seqDB search MLPPAPSRFGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV TQACSMGELLQCGCQAPRGRGPPRPSGLPGTPGPPGPAGPADASAAWEWGGCGDDVDFGD EKSRLFMDAQHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE LSLCL NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atgctgccgcccgcgccctcccggttcgggttgctgctgctgctgctcctgtgtccggcg cacgtcggaggactctggtgggccgtgggcagccccttggtcatggaccccaccagcatc tgcaggaaggcacggcggctggcagggcggcaggcagagctgtgccaggccgagccggaa gtggtggcagagctagcccgtggcgcccgactcggggtgcgagagtgccagttccagttc cgcttccgccgctggaactgctccagccacagcaaggccttcggccgaatcctgcagcag gacattcgggagacggccttcgtgttcgccatcaccgcggcaggtgccagccacgcggtc acgcaggcctgttccatgggcgagctgctgcaatgcggctgccaggccccccgcgggcgg ggcccgcctcggccctccggcctaccaggcaccccgggccccccgggtcccgcgggcccc gcggacgccagcgccgcctgggagtggggaggctgcggcgacgacgtggacttcggggac gagaaatcgaggctcttcatggacgcgcagcacaagcggggccgcggggacatccgcgcg ctggtgcagctgcacaacaacgaagcgggccggctggccgtgcggagccacacgcgcacc gagtgtaagtgccacgggctgtccggctcatgcgccctgcgcacctgctggcagaagctg cccccgttccgcgaggtgggcgcgcggctgctggagcgcttccacggtgcctcgcgcgtc atgggcaccaacgacggcaaggccctgctgcccgccgtccgcacgctcaagcccccgggc cgcgccgacctcctctacgcggccgactcgcccgacttctgcgcccccaaccggcgcacc ggctctccgggcacgcgcggccgcgcctgcaacagcagtgccccggacctcagcggctgc gacctgttgtgctgcggccgcgggcaccgccaggagagcgtgcagctcgaggagaactgc ctgtgccgcttccactggtgctgcgtggtgcagtgccaccgctgccgcgtgcgcaaagag ctcagcctctgcctctga

Oryctolagus cuniculus (rabbit): 100349579 Help Entry 100349579         CDS       T03373                                  Gene name WNT5B Definition (RefSeq) Wnt family member 5B   KO K00444   wingless-type MMTV integration site family, member 5 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04360   Axon guidance ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100349579 (WNT5B)    04390 Hippo signaling pathway     100349579 (WNT5B)    04150 mTOR signaling pathway     100349579 (WNT5B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100349579 (WNT5B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100349579 (WNT5B)   09158 Development and regeneration    04360 Axon guidance     100349579 (WNT5B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100349579 (WNT5B)    05205 Proteoglycans in cancer     100349579 (WNT5B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100349579 (WNT5B)    05226 Gastric cancer     100349579 (WNT5B)    05217 Basal cell carcinoma     100349579 (WNT5B)    05224 Breast cancer     100349579 (WNT5B)   09164 Neurodegenerative disease    05010 Alzheimer disease     100349579 (WNT5B)    05022 Pathways of neurodegeneration - multiple diseases     100349579 (WNT5B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100349579 (WNT5B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100349579 (WNT5B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100349579 (WNT5B) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100349579 (WNT5B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100349579 NCBI-ProteinID:  XP_002712821 Ensembl:  ENSOCUG00000013686 LinkDB All DBs Position 8 AA seq 359 aa AA seqDB search MPSLLLLFTAALLSSWAQLLADASSWWSLAMSPVQRPEMFIIGAQPVCSQLPGLSPGQRK LCQLYQEHMAYIGEGAKMGIKECQYQFRQRRWNCSTVDNSSVFGRVMQIGSRETAFTYAV SAAGVVNAISRACREGELSTCGCSRTARPKDLPRDWLWGGCGDNVEYGYRFAKEFVDARE REKNFAKGSEEQGRVLMNLQNNEAGRRAVYKMADVACKCHGVSGSCSLKTCWLQLAEFRK VGDQLKEKYDSAAAMRITRKGKLELVNSRFNQPTPEDLVYVDPSPDYCLRNETTGSLGTQ GRICNKTSEGMDGCELMCCGRGYDQFKSVQVERCHCKFHWCCFVKCKKCTEIVDQYVCK NT seq 1080 nt NT seq  +upstreamnt  +downstreamnt atgcccagcctgctgctgctgttcactgctgctctgctctccagctgggcccagctcctg gcagacgccagctcctggtggtccttagccatgagcccggtgcagagacctgagatgttt atcatcggcgctcagcctgtgtgcagtcagcttcccgggctctcccctggccagagaaag ctgtgccagctgtaccaggagcacatggcctacattggagagggagccaagatgggcatc aaggagtgccagtaccagttccggcagaggcggtggaattgcagcacggtggacaactcg tccgtctttgggagagtcatgcagataggcagccgcgagacggccttcacctacgccgtg agcgccgcgggggtggtgaacgccatcagccgggcctgccgcgagggcgagctgtccacc tgtggctgcagccggacagcgcggcccaaggacctgccccgggactggctgtggggtggc tgcggggacaacgtggaatacggctaccgctttgctaaggagtttgtggacgcccgggag cgggagaagaacttcgccaagggatcggaggagcagggccgcgtgctcatgaacctgcag aacaacgaggcaggcagaagggctgtgtacaagatggcagacgtagcctgcaagtgccac ggcgtctccggctcctgcagcctcaagacgtgctggctgcagctggccgagttccgcaag gtgggggaccagctgaaggagaagtacgacagcgcggccgccatgcgcatcacccgcaag ggcaagctggagctggtcaacagccgcttcaaccagcccacgcccgaggacctggtctac gtggaccccagccctgactactgcctgcgcaacgagaccacgggctcgctgggcacgcag ggccgcatctgcaacaagacctcggagggcatggacggctgtgagctcatgtgctgcggc cgcggctacgaccagttcaagagcgtgcaggtggagcgctgccactgcaagttccactgg tgctgctttgtcaagtgcaagaagtgcacggagatcgtggaccagtacgtctgcaaatag

Oryctolagus cuniculus (rabbit): 100349847 Help Entry 100349847         CDS       T03373                                  Gene name WNT2B Definition (RefSeq) Wnt family member 2B   KO K00182   wingless-type MMTV integration site family, member 2 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100349847 (WNT2B)    04390 Hippo signaling pathway     100349847 (WNT2B)    04150 mTOR signaling pathway     100349847 (WNT2B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100349847 (WNT2B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100349847 (WNT2B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100349847 (WNT2B)    05205 Proteoglycans in cancer     100349847 (WNT2B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100349847 (WNT2B)    05226 Gastric cancer     100349847 (WNT2B)    05217 Basal cell carcinoma     100349847 (WNT2B)    05224 Breast cancer     100349847 (WNT2B)   09164 Neurodegenerative disease    05010 Alzheimer disease     100349847 (WNT2B)    05022 Pathways of neurodegeneration - multiple diseases     100349847 (WNT2B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100349847 (WNT2B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100349847 (WNT2B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100349847 (WNT2B) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100349847 (WNT2B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Herpes_LMP1 Motif Other DBs NCBI-GeneID:  100349847 NCBI-ProteinID:  XP_002715814 Ensembl:  ENSOCUG00000000266 UniProt:  G1THI6 LinkDB All DBs Position 13 AA seq 397 aa AA seqDB search MLRPGGAEEAAQLPPRRARAPAPAPAPAPAPRPAAPDGSPASARLGLACLLLLLLLTLPA RVDSSWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHH RWNCTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRG RHHDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLK LECKCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRA TRTDLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQ CECKFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT NT seq 1194 nt NT seq  +upstreamnt  +downstreamnt atgctgaggccgggtggtgcagaggaagccgcgcagctcccccctcggcgcgcccgcgcc cctgcccctgcccctgcccctgcccccgcgcccagacccgcggcccccgacggctccccg gcttcggcccgcctaggtcttgcctgcctgctgctgctgctgctgttgacgctgccagcc cgcgtcgattcgtcttggtggtacatcggggcactgggggcccgagtgatctgtgacaat atccctggtttggtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgc tcggtgggcgaaggtgcccgggaatggatccgagagtgtcagcaccagttccgccaccac cgctggaactgcaccacactggaccgggaccacactgtctttggtcgtgtcatgctcaga agtagccgggaggcagcttttgtatatgccatctcatccgcaggggtggtccatgccatc actcgagcctgtagccagggtgaactgagtgtatgcagctgtgacccctacacgcgtggc cgacaccacgaccaacgtggggactttgactggggtggctgcagtgacaacatccactat ggcgtccgctttgccaaggccttcgtggatgccaaggagaagaggctgaaggatgcccgg gccctcatgaacttacataacaaccgctgtgggcgcacggctgtgcggcggtttctgaag ctggagtgcaagtgccacggcgtgagtggctcctgtactctgcgcacctgctggcgtgca ctctcagacttccgtcgcacaggtgattacttgcgacggcgctacgatggggctgtgcag gtgacagccacccaggacggtgccaacttcacagcagcccgccaaggctatcgccgtgcc acccggactgatcttgtctacttcgacaactcccctgactactgtgtcttggacaaggct gcaggttccctaggcactgctggccgtgtctgcagcaagacatcgaaaggaacggacggc tgtgaaatcatgtgctgtggccgtgggtacgacacgactcgagttacccgtgtcacccag tgtgagtgcaaattccactggtgctgtgcggtgcgctgcaaggaatgcagaaacactgtg gacgtccatacttgcaaggcccccaagaaggcagagtggctagaccagacctga

Oryctolagus cuniculus (rabbit): 100351316 Help Entry 100351316         CDS       T03373                                  Gene name WNT10B Definition (RefSeq) Wnt family member 10B   KO K01357   wingless-type MMTV integration site family, member 10 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100351316 (WNT10B)    04390 Hippo signaling pathway     100351316 (WNT10B)    04150 mTOR signaling pathway     100351316 (WNT10B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100351316 (WNT10B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100351316 (WNT10B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100351316 (WNT10B)    05205 Proteoglycans in cancer     100351316 (WNT10B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100351316 (WNT10B)    05226 Gastric cancer     100351316 (WNT10B)    05217 Basal cell carcinoma     100351316 (WNT10B)    05224 Breast cancer     100351316 (WNT10B)   09164 Neurodegenerative disease    05010 Alzheimer disease     100351316 (WNT10B)    05022 Pathways of neurodegeneration - multiple diseases     100351316 (WNT10B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100351316 (WNT10B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100351316 (WNT10B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100351316 (WNT10B) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100351316 (WNT10B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100351316 NCBI-ProteinID:  XP_002711122 Ensembl:  ENSOCUG00000009580 UniProt:  G1SXH3 LinkDB All DBs Position 4 AA seq 389 aa AA seqDB search MLEEPQQRTLPLGLAGLLLLAVCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLG LCLRSPDVTASALQGLHVAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS FSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRSKLLQLQALSRGKSFPHSLPSP GPGSGSSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLR PRRLSGELVYFEKSPDFCERDPTVGSPGTRGRACNKTSRLLDGCGSLCCGRGHNVLRQTR VERCHCRFHWCCYVLCDECKVTEWVNVCK NT seq 1170 nt NT seq  +upstreamnt  +downstreamnt atgctggaggagccccagcagcggactctgcccttgggcctcgcgggtctcctgctcctt gcggtgtgcagtcgggcgctcagcaatgagattctgggcctgaagctgcccggggagccg ccgctgacggccaacaccgtgtgcttgacgctgtccggcctaagcaagcgccagttgggc ctgtgcctgcgcagccccgacgtgacggcctctgcgcttcagggtctgcacgtcgccgtg cacgagtgccagcaccagctgcgcgaccagcgctggaactgctcggcactcgagggcggc ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgcgagagtgccttctcc ttctccatgctggctgctggggtaatgcatgcagtagccacagcctgcagcctgggcaag ctggtgagctgtggctgtggctggaagggcagcggtgaacaggatcggctcaggtccaaa ctgctgcagctgcaggcgctgtcccggggcaagagttttccccactccctgcccagccct ggccccggctcaggctccagccctggcccccaggacacgtgggaatggggtggctgtaac catgacatggactttggagagaagttctctcgggacttcttggattccagggaagctccc cgggacatccaggcgagaatgagaatccataacaacagggtggggcgccaggtggtaact gaaaacctgaagcggaaatgcaagtgccatggcacttcgggcagctgccagtttaaaacc tgctggagggcagccccagagttccgggccgtgggggcagcgctgagggagcggctgggc cgagccatcttcattgacacccacaaccgcaattccggagccttccaaccccgcctgcgt ccccggcgcctctcaggagagctggtctactttgagaagtctcccgacttctgcgagcga gaccccacggtgggctccccgggcacgagaggccgggcttgcaacaagaccagccgcctg ctggatggctgcgggagcctgtgctgcggccgcgggcacaacgtgctccggcagacgcga gttgagcgctgccactgccgcttccactggtgctgctatgtgctgtgtgacgagtgcaaa gtcacggaatgggtcaatgtgtgcaagtga

Oryctolagus cuniculus (rabbit): 100352227 Help Entry 100352227         CDS       T03373                                  Gene name WNT9A Definition (RefSeq) Wnt family member 9A   KO K01064   wingless-type MMTV integration site family, member 9 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100352227 (WNT9A)    04390 Hippo signaling pathway     100352227 (WNT9A)    04150 mTOR signaling pathway     100352227 (WNT9A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100352227 (WNT9A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100352227 (WNT9A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100352227 (WNT9A)    05205 Proteoglycans in cancer     100352227 (WNT9A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100352227 (WNT9A)    05226 Gastric cancer     100352227 (WNT9A)    05217 Basal cell carcinoma     100352227 (WNT9A)    05224 Breast cancer     100352227 (WNT9A)   09164 Neurodegenerative disease    05010 Alzheimer disease     100352227 (WNT9A)    05022 Pathways of neurodegeneration - multiple diseases     100352227 (WNT9A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100352227 (WNT9A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100352227 (WNT9A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100352227 (WNT9A) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100352227 (WNT9A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Clr5 Motif Other DBs NCBI-GeneID:  100352227 NCBI-ProteinID:  XP_008250998 Ensembl:  ENSOCUG00000026170 LinkDB All DBs Position Un AA seq 404 aa AA seqDB search MGTGRSQRVPSCLRPPAGPFWGAWSHTAPGPVHSGRALHGVPPLALPSPTHRPAPATLLW ARAHPHLSVPRLTGSEPLTILPLSLEPEAAAQAHYKACDRLKLERKQRRMCRRDPGVAET LVEAVSMSALECQYQFRFERWNCTLEGRYRASLLKRGFKETAFLYAISSAGLTHALAKAC SAGRMERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVKEFLGRRSSKDLRARVDFHNNL VGVKVIKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVGKHLKHKYETALKVGSTTNEAT GEAGAISPPRGRASGMGGSDPLPRTPELVHLDDSPSFCLAGRFSPGTAGRRCHREKNCES ICCGRGHNTQSRVVTRPCQCQVRWCCYVECRQCTQREEVYTCKG NT seq 1215 nt NT seq  +upstreamnt  +downstreamnt atggggactggcaggtcccaaagggtcccttcttgcctccggccccctgcaggccctttc tggggtgcctggtcccacaccgctcctgggcctgtacactcaggccgggctctgcatggt gttcctccgctggcgctccccagccccacccaccgccctgccccagccaccctgctctgg gccagggctcaccctcacctctccgtgcccaggctaacgggcagcgagcccctgaccatc ctccctctgagcctggaacccgaggcggctgcccaggcgcactacaaagcgtgcgaccgg ctgaagctggagcggaagcaacggcgcatgtgccgccgggacccgggcgtggccgagacg ctggtggaggcggtgagcatgagtgcgctcgagtgccagtaccagttccgcttcgagcgc tggaactgcacgctggagggccgctaccgcgccagcctgctgaagcgaggcttcaaggag acggccttcctctacgccatctcctcggccggactgacgcacgcgctggccaaggcgtgc agcgcggggcgcatggagcgctgtacgtgcgacgaggcgcccgacctggagaaccgcgag gcctggcagtggggcggctgtggcgacaacctcaagtacagcagcaagttcgtcaaggag ttcctgggccggcggtccagcaaggacctgcgagcacgtgtggacttccataacaacctc gtgggcgtgaaggtgatcaaggccggggtggagaccacatgcaagtgccacggtgtgtct ggctcatgcacggtgcggacctgctggcggcagctggcgcccttccacgaggtgggcaag cacctgaagcacaagtatgagactgcactcaaggtgggcagcaccaccaacgaagccact ggcgaggcgggcgccatctccccgccacggggccgggcctcggggatgggcggcagtgac cccctgccccgcacaccagagctcgtacacctggacgactcgcccagcttctgcctggct ggccgcttctccccaggcaccgctggccgcaggtgccaccgggagaagaactgtgagagc atctgctgtggccgcggccacaacacacagagccgggtggtgacaagaccctgccagtgc caggtgcgctggtgctgctatgtggagtgtcgacagtgcacgcagcgcgaggaggtctac acctgcaagggctga

Oryctolagus cuniculus (rabbit): 100352839 Help Entry 100352839         CDS       T03373                                  Gene name WNT10A Definition (RefSeq) Wnt family member 10A   KO K01357   wingless-type MMTV integration site family, member 10 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100352839 (WNT10A)    04390 Hippo signaling pathway     100352839 (WNT10A)    04150 mTOR signaling pathway     100352839 (WNT10A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100352839 (WNT10A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100352839 (WNT10A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100352839 (WNT10A)    05205 Proteoglycans in cancer     100352839 (WNT10A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100352839 (WNT10A)    05226 Gastric cancer     100352839 (WNT10A)    05217 Basal cell carcinoma     100352839 (WNT10A)    05224 Breast cancer     100352839 (WNT10A)   09164 Neurodegenerative disease    05010 Alzheimer disease     100352839 (WNT10A)    05022 Pathways of neurodegeneration - multiple diseases     100352839 (WNT10A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100352839 (WNT10A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100352839 (WNT10A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100352839 (WNT10A) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100352839 (WNT10A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100352839 NCBI-ProteinID:  XP_002712529 Ensembl:  ENSOCUG00000016033 UniProt:  G1TAR3 LinkDB All DBs Position 7 AA seq 417 aa AA seqDB search MGSAHPRPWLRLRPRPQPRPPLWALLFFLLLLAAAVPRSAPNDILGLRLPPEPVLNANTV CLTLPGLSRRQMEVCVRHPDVAASAIQGIQIAIHECQHQFRDQRWNCSSLETRNKIPYES PIFSRGFRESAFAYAIAAAGVVHAVSNACALGKLRACGCDASRRGDEEAFRRKLHRLQLD ALQRGKGLSHGVPEHPALPPASPGLQDSWEWGGCSPDVGFGERFSKDFLDSREPHRDIHA RMRLHNNRVGRQAVMDNMRRKCKCHGTSGSCQLKTCWQVTPEFRAVGALLRNRFHRATLI RPHNRNGGQLEPGPAGAPSPAPGTPGPRRRASPADLVYFEKSPDFCEREPRLDSAGTVGR LCNKSSAGPDGCGSMCCGRGHNILRQTRSERCHCRFHWCCFVVCEECRITEWVSVCK NT seq 1254 nt NT seq  +upstreamnt  +downstreamnt atgggcagcgcccaccctcgcccctggctgcggctccgaccccggccccagccgcggccc ccgctctgggcgctcctgttcttcctactgctgctggctgctgccgtgcccaggtcagca cccaacgacatcctcggcctccgcctgcccccggagcccgtgctcaacgccaacacggtg tgcttgacgttgcccggcctgagccggcggcagatggaggtgtgtgtgcgccacccggac gtggccgcctcggccatccagggcattcagatcgccatccacgagtgccaacaccagttc cgggaccagcgctggaactgctccagcctcgagactcgcaacaagatcccctacgagagc cccatcttcagcagaggtttccgagagagcgccttcgcctatgccatcgcggcagccggt gtggtgcacgccgtgtccaacgcgtgcgccctgggcaaactgcgggcgtgcggctgcgac gcgtcccggcgcggggatgaggaggcctttcgtcggaagctgcaccgcttgcagctggac gcgctgcaacgtggaaagggcctgagccacggggtcccggagcaccccgccctgcccccc gccagcccgggcctgcaggactcctgggagtggggcggctgcagcccggatgtgggtttc ggcgagcgcttctctaaggactttctggactcccgggagcctcaccgagacatccacgcg cgcatgaggctccacaacaaccgggtcggtaggcaggcggtgatggacaacatgcggcgg aagtgcaagtgtcacggcacgtcgggcagctgccagctcaagacgtgctggcaggtgacg cccgagttccgcgccgtgggggcgctgctgcgcaaccgcttccaccgcgccacgctcatc cggccgcacaaccgcaacggcggccagctggaacccggcccggcgggggcgccgtcccca gcgccgggcacccccgggccgcgccgtcgggccagccccgccgacctggtctactttgag aagtcacccgacttctgcgagcgcgagccgcgcctggactcggcgggcaccgtgggccgc ctgtgcaacaagagcagcgcgggccccgacggctgcggcagcatgtgctgcggccgcggc cacaacatcctacgccagacccgcagcgaacgctgccactgccgcttccactggtgctgc ttcgtggtctgcgaagagtgccgcatcaccgagtgggtcagcgtctgcaagtga

Oryctolagus cuniculus (rabbit): 100353090 Help Entry 100353090         CDS       T03373                                  Gene name WNT16 Definition (RefSeq) Wnt family member 16   KO K01558   wingless-type MMTV integration site family, member 16 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05202   Transcriptional misregulation in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100353090 (WNT16)    04390 Hippo signaling pathway     100353090 (WNT16)    04150 mTOR signaling pathway     100353090 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100353090 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100353090 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100353090 (WNT16)    05202 Transcriptional misregulation in cancer     100353090 (WNT16)    05205 Proteoglycans in cancer     100353090 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100353090 (WNT16)    05226 Gastric cancer     100353090 (WNT16)    05217 Basal cell carcinoma     100353090 (WNT16)    05224 Breast cancer     100353090 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     100353090 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     100353090 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100353090 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100353090 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100353090 (WNT16) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100353090 (WNT16) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100353090 NCBI-ProteinID:  XP_002712150 Ensembl:  ENSOCUG00000014744 UniProt:  G1U287 LinkDB All DBs Position 7 AA seq 365 aa AA seqDB search MDRAALLGLPRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLSGRQKELC KRKPYLLPSIREGARLGIQECRSQFRHERWNCRVAAPAAAAPLGTGPLFGYELSSGTKET AFIYAVMAAGLVHAVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSR KFLDFPIRNTTGKDSKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMS SFEKIGHLLKDKYENSIQISEKTKKKMHRREKDQRKLPIRKEDLLYVNKSPNYCVEDKKL GIPGTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTD VHTCK NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atggaccgagcggcgctcctgggactgccacgcctgtgcgcgctgtgggcagccctgctc gcgctgtttccctgcggagcccaaggaaactggatgtggttgggcatcgcctcctttggc gtcccggagaagctgggctgcgccaacttgccgctgagcggccgccagaaggagctgtgc aagaggaaaccgtacctgctgccgagcatccgcgagggcgcgcgcctgggcatccaggag tgcaggagtcagttccggcacgagcgctggaactgcagggtcgccgccccggccgccgcc gcgccgctcggcactgggcccctcttcggctacgagctgagcagcggcaccaaggagaca gcatttatttatgctgtaatggctgcaggcctggtgcatgctgtgaccaggtcctgtagt gcaggcaacatgacagaatgctcctgtgacaccaccttgcagaacggtgggtcggcaagc gaaggctggcactgggggggctgctccgatgatgtccagtatggcatgtggttcagcagg aagttcctagactttcccatcagaaacaccacagggaaggacagcaaagtactgctagca atgaatctacataacaatgaagctgggaggcaggctgtcgccaagttgatgtcagtagac tgccgctgccacggagtttctggctcttgtgctgttaaaacatgctggaaaaccatgtct tcctttgaaaagatcggccatttgttgaaggataaatatgaaaatagtattcagatatca gagaaaacaaagaagaaaatgcaccggagagaaaaagatcagaggaaactaccgattcgc aaggaagatctgctctatgtcaataagtctcccaactactgtgtggaggacaagaaactg ggcatcccagggactcaaggcagagaatgcaaccgcacttcggaaggggctgacggctgc aacctcttatgctgtggccgaggatacaacacccatgtggtcaggcacgtggagaggtgt gagtgtaagtttatctggtgctgctacgtccgctgcagaagatgcgaaagcatgactgat gtccacacgtgtaagtaa

Oryctolagus cuniculus (rabbit): 100353559 Help Entry 100353559         CDS       T03373                                  Gene name WNT9B Definition (RefSeq) Wnt family member 9B   KO K01064   wingless-type MMTV integration site family, member 9 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100353559 (WNT9B)    04390 Hippo signaling pathway     100353559 (WNT9B)    04150 mTOR signaling pathway     100353559 (WNT9B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100353559 (WNT9B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100353559 (WNT9B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100353559 (WNT9B)    05205 Proteoglycans in cancer     100353559 (WNT9B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100353559 (WNT9B)    05226 Gastric cancer     100353559 (WNT9B)    05217 Basal cell carcinoma     100353559 (WNT9B)    05224 Breast cancer     100353559 (WNT9B)   09164 Neurodegenerative disease    05010 Alzheimer disease     100353559 (WNT9B)    05022 Pathways of neurodegeneration - multiple diseases     100353559 (WNT9B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100353559 (WNT9B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100353559 (WNT9B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100353559 (WNT9B) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100353559 (WNT9B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100353559 NCBI-ProteinID:  XP_017204738 LinkDB All DBs Position 19 AA seq 380 aa AA seqDB search MQPLRPACRPGGRCLEPPGSPPIPRALHPWSAPTVSPEAHPLPPLIPSSLTGREVLTPFP GLGTAAAPAQGGAHLKQCDLLKLSRRQKQLCRREPGLAETLRDAARLGLLECQFQFRQER WNCSLEGRTGLLKRGFKETAFLYAVSSAALTHALARACSAGRMERCTCDDSPGLQSRQAW QWGVCGDNLKYSTKFLSNFLGPKRGSKDLRARVDAHNTHVGIKAVKSGLRTTCKCHGVSG SCAVRTCWKQLAPFRETGEVLKLRYDSAVKVSSATNEALGRLELWAPSKPGSPAKGLAPR PGDLVYLEDSPSFCRPSKYSPGTAGRVCSREASCGSLCCGRGYDTQSRLVAFSCHCQVQW CCYVECQQCVQEELVYTCKH NT seq 1143 nt NT seq  +upstreamnt  +downstreamnt atgcagccgctgaggccggcctgccgcccaggagggagatgcttggagcccccaggaagc ccccccatccccagggctctgcacccttggtccgcacccactgtgtcccccgaggctcat cccctccctcctctcatcccttccagcttgaccgggcgcgaggtcctgacgcccttcccc ggcctgggcactgcggcggccccggcacaggggggcgcccacctgaagcagtgcgacctg ctgaagctgtcccgccggcagaagcagctgtgccggcgcgagcccggcctggcagagacc ctgcgggacgccgcgcgcctcggcctgctcgagtgccagttccagttccggcaggagcgc tggaactgcagcctggaggggaggaccgggctgctcaagagaggcttcaaggagacggcc ttcctgtacgcagtgtcctcggccgccctcacccacgcgctggcccgggcctgcagcgcc gggcgcatggagcgctgcacctgcgatgactccccggggctgcagagccggcaggcctgg cagtggggcgtgtgtggcgacaacctcaagtacagcaccaagtttctgagcaacttcctg ggacccaagcgaggaagcaaggacctgcgggcacgggtggacgcccacaacacccacgtg ggcatcaaggctgtgaagagcggcctcaggaccacgtgtaagtgccacggcgtgtcgggc tcctgtgcggtgcgcacctgctggaagcagcttgccccgttccgcgagacgggcgaggtg ctgaaactgcgctatgactcagctgtcaaggtgtccagcgccaccaacgaggccttgggc cgcctggagctctgggccccctccaagccaggcagccccgccaagggcctggccccccgg cccggggacctggtctacctggaagactcgcccagcttctgccggcccagcaaatactct cccggcacggcgggcagggtgtgctcccgggaggccagctgcggcagcctgtgctgtggg cggggctacgacacgcagagtcgcctggtggccttctcctgccactgccaggtgcagtgg tgctgctacgtggagtgccagcagtgcgtgcaggaggagctggtgtacacctgtaagcac tag

Oryctolagus cuniculus (rabbit): 100354018 Help Entry 100354018         CDS       T03373                                  Gene name WNT1 Definition (RefSeq) Wnt family member 1   KO K03209   wingless-type MMTV integration site family, member 1 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100354018 (WNT1)    04390 Hippo signaling pathway     100354018 (WNT1)    04150 mTOR signaling pathway     100354018 (WNT1)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100354018 (WNT1)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100354018 (WNT1)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100354018 (WNT1)    05205 Proteoglycans in cancer     100354018 (WNT1)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100354018 (WNT1)    05226 Gastric cancer     100354018 (WNT1)    05217 Basal cell carcinoma     100354018 (WNT1)    05224 Breast cancer     100354018 (WNT1)   09164 Neurodegenerative disease    05010 Alzheimer disease     100354018 (WNT1)    05022 Pathways of neurodegeneration - multiple diseases     100354018 (WNT1)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100354018 (WNT1)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100354018 (WNT1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100354018 (WNT1) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100354018 (WNT1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100354018 NCBI-ProteinID:  XP_002711131 Ensembl:  ENSOCUG00000026066 UniProt:  G1U5M0 LinkDB All DBs Position 4 AA seq 370 aa AA seqDB search MGCWALLPSWVSPALLLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTAPGPHLFGKIVNRG CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR AVGDVLRDRFDGASRVLYGNRGSNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT YSGRLGTAGTTGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC THTRVLHECL NT seq 1113 nt NT seq  +upstreamnt  +downstreamnt atggggtgctgggcgctgctgcccagctgggtttctcctgcgctgctactggcgctggcc gccctgcccgcagctctggcggccaacagcagcggccgatggtggggcatcgtaaacgtc gcttcctccacgaacctgctaactgactccaagagcctgcagctggtgctggagcccagt ctgcagctcctgagccgcaaacagcggcgcctgatccggcagaacccaggcatcctgcac agcgtgagcggggggctgcagagcgccgtgcgcgagtgcaagtggcaattccggaaccgc cgctggaactgccccaccgcgccggggccccacctcttcggcaagatcgtcaaccgaggc tgccgggaaacagcttttatcttcgccatcacctctgcgggggtcacccactcggtggcg cgctcctgctccgagggttccatcgagtcttgcacgtgcgactatcggcggcgcggcccc gggggccccgactggcactgggggggctgcagcgacaacatcgacttcggccgcctcttt ggcagggaattcgtggactccggggagaaggggcgggacttgcgctttctcatgaacctg cacaacaacgaggcgggccgcacgaccgtcttctctgagatgcgccaggagtgcaagtgc cacggcatgtcgggctcgtgcaccgtgcgcacgtgctggatgcggctgcccacgctgcgc gccgtgggcgacgtgctgcgcgaccgcttcgacggcgcctcgcgcgttctctacggcaac cgcggtagcaaccgcgcttcgcgggcggagctgctgcgcctggagcccgaggacccggcg cacaagccgccctccccacacgacctggtctactttgagaaatcgcccaacttctgcacg tacagcggacgcctgggcaccgcgggcaccacggggcgagcctgcaacagctcgtcgccg gctctggacggctgcgagctgctgtgctgcggtcggggccaccgcacgcgcacgcagcgc gtcaccgagcgctgcaattgcaccttccactggtgctgtcatgtcagctgccgcaactgc acgcatacgcgcgtgctgcacgagtgtctgtga

Oryctolagus cuniculus (rabbit): 100354583 Help Entry 100354583         CDS       T03373                                  Gene name WNT3A Definition (RefSeq) Wnt family member 3A   KO K00312   wingless-type MMTV integration site family, member 3 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05206   MicroRNAs in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100354583 (WNT3A)    04390 Hippo signaling pathway     100354583 (WNT3A)    04150 mTOR signaling pathway     100354583 (WNT3A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100354583 (WNT3A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100354583 (WNT3A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100354583 (WNT3A)    05206 MicroRNAs in cancer     100354583 (WNT3A)    05205 Proteoglycans in cancer     100354583 (WNT3A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100354583 (WNT3A)    05226 Gastric cancer     100354583 (WNT3A)    05217 Basal cell carcinoma     100354583 (WNT3A)    05224 Breast cancer     100354583 (WNT3A)   09164 Neurodegenerative disease    05010 Alzheimer disease     100354583 (WNT3A)    05022 Pathways of neurodegeneration - multiple diseases     100354583 (WNT3A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100354583 (WNT3A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100354583 (WNT3A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100354583 (WNT3A) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100354583 (WNT3A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100354583 NCBI-ProteinID:  XP_002723899 Ensembl:  ENSOCUG00000004048 UniProt:  G1SKY6 LinkDB All DBs Position Un AA seq 351 aa AA seqDB search MAPLGYFLLLCSLRPALGSYPIWWSLAVGPQHSSLGTHPVLCASIPGLVPKQLRFCRNYV EIMPSVAEGVRLAVQECQHQFRGRRWNCTTVDSLAIFGPVLDRATRESAFVHAIASAGVA FAVTRSCAEGSATICGCSSRHPGSPGEGWKWGGCSEDIEFGGMVSREFADARENRPDARS AMNRHNNEAGRQAIASHVHLKCKCHGLSGSCEVKTCWRAQPAFRAVGDLLKDKYDSASEM VVEKHREARGWVETLRPRYAHFKVPTERDLVYYEASPNFCEPNPDTGSFGTRDRACNVSS PGIDGCDLLCCGRGHNARTERRREKCRCVFHWCCYVSCHECARVLDVHTCK NT seq 1056 nt NT seq  +upstreamnt  +downstreamnt atggctccgctgggatacttcttgctgctgtgcagcttgaggccggcgctgggcagctac cccatctggtggtccctggccgtcgggccgcagcactcctcgctgggcacgcatcccgtg ctgtgtgccagcatccccggcctggtgcccaagcagctgcgcttctgcaggaactacgtg gagatcatgcccagcgtggcggagggcgtgcggctggccgtccaggagtgtcagcaccag ttccgcggccgccgctggaactgcaccaccgtcgacagcctggccatcttcggccctgtg ctggacagagccacccgggagtcagccttcgtgcacgccattgcctccgctggcgtggcc tttgctgtgacgcgttcctgcgcagagggctcagccaccatctgcggctgcagcagccgt cacccgggctcccctggtgagggctggaagtggggcggctgcagtgaggacatcgagttt ggtgggatggtgtcacgggagtttgccgacgcccgggagaaccggccggatgcccgctca gccatgaaccgccacaacaacgaggccgggcgccaggccatcgccagccacgtgcacctg aagtgcaagtgccacgggctgtccggcagctgcgaggtgaagacctgctggcgcgcgcag ccggccttccgagccgtgggcgacctgctcaaggacaagtacgacagcgcctcggagatg gtggtggagaagcaccgcgaggcgcgcggctgggtagagacgctgcggccgcgctacgcc cacttcaaggtgcccacggaacgcgacctggtctattacgaggcctcgcccaacttctgc gagcccaaccctgacacgggctccttcggcacgcgcgaccgcgcctgcaatgtgagctca cccggcatcgacggctgtgacctgctgtgctgcggccgcggccacaacgcacgcaccgag cggcgtcgggagaagtgccgctgcgtcttccactggtgctgctacgtgagctgccacgag tgcgcacgcgtgctggacgtgcatacctgcaagtag

Oryctolagus cuniculus (rabbit): 100355697 Help Entry 100355697         CDS       T03373                                  Gene name WNT7A Definition (RefSeq) Wnt family member 7A   KO K00572   wingless-type MMTV integration site family, member 7 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100355697 (WNT7A)    04390 Hippo signaling pathway     100355697 (WNT7A)    04150 mTOR signaling pathway     100355697 (WNT7A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100355697 (WNT7A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100355697 (WNT7A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100355697 (WNT7A)    05205 Proteoglycans in cancer     100355697 (WNT7A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100355697 (WNT7A)    05226 Gastric cancer     100355697 (WNT7A)    05217 Basal cell carcinoma     100355697 (WNT7A)    05224 Breast cancer     100355697 (WNT7A)   09164 Neurodegenerative disease    05010 Alzheimer disease     100355697 (WNT7A)    05022 Pathways of neurodegeneration - multiple diseases     100355697 (WNT7A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100355697 (WNT7A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100355697 (WNT7A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100355697 (WNT7A) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100355697 (WNT7A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt COG6 Motif Other DBs NCBI-GeneID:  100355697 NCBI-ProteinID:  XP_008258519 Ensembl:  ENSOCUG00000013432 LinkDB All DBs Position 9 AA seq 349 aa AA seqDB search MNGKARRCLGHLFLSLGMAYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEMYTCK NT seq 1050 nt NT seq  +upstreamnt  +downstreamnt atgaacgggaaggcgcggcgctgcttgggccacctctttctcagcctgggcatggcctac ctccggatcggtggcttctcctcggtggttgctctgggagccagcatcatctgtaacaag atcccaggcctggctcccagacagcgggcgatctgccagagccggccggacgccatcatc gtcataggagaaggctcgcaaatgggcctggacgagtgtcagtttcagttccgcaatggc cgctggaactgctcggcgctgggcgagcgcacggtcttcggaaaggagctcaaagtgggg agccgggaggctgccttcacgtacgccatcatcgctgccggcgtggcccacgccatcaca gcggcctgtacccagggcaacctgagcgactgcggctgcgacaaggagaagcaaggccag taccaccgggacgagggctggaagtggggtggctgctccgccgacatccgctacggcatc ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggacgctcatg aacttgcacaataacgaggcgggccgcaagatcctggaggagaacatgaagctggagtgc aagtgccacggtgtgtcgggctcgtgcaccactaagacctgctggaccacgctgccccag ttccgggagctgggctacgtgctcaaggacaagtacaacgaggccgtgcacgtggagccg gtgcgcgccagccgtaacaagcgtcccaccttcctgaagatcaagaagccactgtcgtac cgcaagcccatggacacggacctggtgtacatcgagaagtcgcccaactactgcgaggag gacccggtgacgggcagcgtgggcacgcagggccgtgcctgcaacaagacggccccccag gccagcggctgcgacctcatgtgctgcggccgcggctacaacacccaccagtacgcccgc gtgtggcagtgcaactgtaagttccactggtgctgctacgtcaaatgcaacacgtgcagc gagcgcactgagatgtacacgtgcaagtga

Oryctolagus cuniculus (rabbit): 100357933 Help Entry 100357933         CDS       T03373                                  Gene name WNT8B Definition (RefSeq) Wnt family member 8B   KO K00714   wingless-type MMTV integration site family, member 8 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100357933 (WNT8B)    04390 Hippo signaling pathway     100357933 (WNT8B)    04150 mTOR signaling pathway     100357933 (WNT8B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100357933 (WNT8B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100357933 (WNT8B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100357933 (WNT8B)    05205 Proteoglycans in cancer     100357933 (WNT8B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100357933 (WNT8B)    05226 Gastric cancer     100357933 (WNT8B)    05217 Basal cell carcinoma     100357933 (WNT8B)    05224 Breast cancer     100357933 (WNT8B)   09164 Neurodegenerative disease    05010 Alzheimer disease     100357933 (WNT8B)    05022 Pathways of neurodegeneration - multiple diseases     100357933 (WNT8B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100357933 (WNT8B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100357933 (WNT8B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     100357933 (WNT8B) Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    100357933 (WNT8B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  100357933 NCBI-ProteinID:  XP_017203983 Ensembl:  ENSOCUG00000000986 UniProt:  G1SEH4 LinkDB All DBs Position 18 AA seq 351 aa AA seqDB search MFREKPCVCVFLFTCVLQLSHTWSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAW DRWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNG QLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTC KCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRS ISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEE RRAETVSSCNCKFHWCCAVRCEQCRRRITKYFCSRAERPRGGAAHKAGRKP NT seq 1056 nt NT seq  +upstreamnt  +downstreamnt atgtttcgggagaagccctgtgtgtgtgtctttctgttcacctgtgtcctccagctcagc cacacctggtccgtgaacaatttcctgatgactggtccaaaggcatacctgatctactcc agcagcgtggcggctggggcccagagcggcattgaggaatgcaagtaccagtttgcctgg gaccgctggaactgcccggagcgcgccctgcagctgtccagccatggcgggctgcgcagt gcgaaccgcgagacggcgttcgtgcacgccatcagctccgccggcgtcatgtacaccctg accaggaactgcagcctgggcgattttgacaactgcggctgtgacgactcccgaaacggg cagctggggggccaaggctggctttggggaggctgcagtgacaacgtgggcttcggagag gccatttccaagcagttcgtcgatgccctggagacaggacaggacgcccgggcggccatg aacctgcacaacaacgaggccggccgcaaggcggtgaagggcaccatgaaacgcacgtgc aagtgccacggcgtgtccggcagctgcaccacgcagacctgctggctgcagctgcccgag ttccgcgaggtgggcgcgcacctcaaagagaagtaccacgcggcgctcaaggtggacctg ctgcagggcgccggcaacagcgcggccggccgcggcgccatcgccgacaccttccgctcc atctccacccgggagctcgtgcacctggaagactccccggactactgcctggagaacaaa acgctagggctgctgggcaccgagggccgagagtgcctgcggcgggggcgggccctgggc cgctgggagcgccgcagctgccgccggctgtgcggggactgcgggctggcggtggaggag cgccgcgccgagaccgtgtccagctgcaactgcaagttccactggtgctgcgccgtccgc tgcgagcagtgccgccggcgcatcaccaagtacttctgcagccgcgcggagcggccgcgg gggggcgctgcccacaaggccgggaggaagccctag

Oryctolagus cuniculus (rabbit): 103347432 Help Entry 103347432         CDS       T03373                                  Definition (RefSeq) protein Wnt-2b-like   KO K00572   wingless-type MMTV integration site family, member 7 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04150   mTOR signaling pathway ocu04310   Wnt signaling pathway ocu04390   Hippo signaling pathway ocu04550   Signaling pathways regulating pluripotency of stem cells ocu04916   Melanogenesis ocu04934   Cushing syndrome ocu05010   Alzheimer disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05165   Human papillomavirus infection ocu05200   Pathways in cancer ocu05205   Proteoglycans in cancer ocu05217   Basal cell carcinoma ocu05224   Breast cancer ocu05225   Hepatocellular carcinoma ocu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103347432    04390 Hippo signaling pathway     103347432    04150 mTOR signaling pathway     103347432  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103347432  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103347432  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103347432    05205 Proteoglycans in cancer     103347432   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103347432    05226 Gastric cancer     103347432    05217 Basal cell carcinoma     103347432    05224 Breast cancer     103347432   09164 Neurodegenerative disease    05010 Alzheimer disease     103347432    05022 Pathways of neurodegeneration - multiple diseases     103347432   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103347432   09172 Infectious disease: viral    05165 Human papillomavirus infection     103347432  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ocu00536]     103347432 Glycosaminoglycan binding proteins [BR:ocu00536]  Heparan sulfate / Heparin   Morphogens    103347432 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103347432 NCBI-ProteinID:  XP_008252185 LinkDB All DBs Position Un AA seq 203 aa AA seqDB search MTLWFRSWVCALEVENRGCDSNLYLHVQGKPGSQSWLRTGRGCGTLPWSSVCSRGWGPRF LRRPGQAGPFQTRITRDRAGVSSCSPGLTAPCLSCLGRALSSVVALGANIICNKIPGLAP RQRAICQSRPDAIIVIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGKGTPGL AWPLGWRGPWAGVAPGLAWPLGW NT seq 610 nt NT seq  +upstreamnt  +downstreamnt atgaccctgtggttccgttcctgggtgtgtgccctagaggtggaaaacaggggctgtgac agcaacttgtacctgcatgtgcagggaaagcccggctcccagagctggctccgcacaggg cgcggctgtgggactctgccctggagctctgtctgctcccggggctgggggcctcggttc ctgcgacgcccaggccaggcgggtcctttccaaacccggatcacgcgggatagggcgggg gtgtcctcctgctcacccggcctcaccgccccatgcctgtcctgtcttggcagagcgctg tcgtcggtggtggccctgggagccaacatcatctgcaacaagattcccggcttggcaccg cggcaacgcgccatctgccagagccggcccgacgccatcatcgtcatcggggagggggca cagatgggcatcaacgagtgccagtaccagttccgcttcggccgctggaactgctcggcc ctgggcgagaagaccgtgttcgggcaggagctccgagtcggtaagggcacccctgggctg gcgtggcccctgggctggcgtggcccctgggctggagtggcccctgggctggcgtggccc ctgggctgga

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