Oryx dammah (scimitar-horned oryx): 120858471 Help Entry 120858471         CDS       T07255                                  Symbol WNT7B Name (RefSeq) protein Wnt-7b   KO K00572   wingless-type MMTV integration site family, member 7 Organism oda  Oryx dammah (scimitar-horned oryx) Pathway oda04150   mTOR signaling pathway oda04310   Wnt signaling pathway oda04390   Hippo signaling pathway oda04550   Signaling pathways regulating pluripotency of stem cells oda04916   Melanogenesis oda04934   Cushing syndrome oda05010   Alzheimer disease oda05022   Pathways of neurodegeneration - multiple diseases oda05165   Human papillomavirus infection oda05200   Pathways in cancer oda05205   Proteoglycans in cancer oda05217   Basal cell carcinoma oda05224   Breast cancer oda05225   Hepatocellular carcinoma oda05226   Gastric cancer Brite KEGG Orthology (KO) [BR:oda00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     120858471 (WNT7B)    04390 Hippo signaling pathway     120858471 (WNT7B)    04150 mTOR signaling pathway     120858471 (WNT7B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     120858471 (WNT7B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     120858471 (WNT7B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     120858471 (WNT7B)    05205 Proteoglycans in cancer     120858471 (WNT7B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     120858471 (WNT7B)    05226 Gastric cancer     120858471 (WNT7B)    05217 Basal cell carcinoma     120858471 (WNT7B)    05224 Breast cancer     120858471 (WNT7B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     120858471 (WNT7B)   09164 Neurodegenerative disease    05010 Alzheimer disease     120858471 (WNT7B)    05022 Pathways of neurodegeneration - multiple diseases     120858471 (WNT7B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     120858471 (WNT7B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:oda00536]     120858471 (WNT7B) Glycosaminoglycan binding proteins [BR:oda00536]  Heparan sulfate / Heparin   Morphogens    120858471 (WNT7B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  120858471 NCBI-ProteinID:  XP_040090481 LinkDB All DBs Position Unknown AA seq 349 aa AA seqDB search MHRNFRKWIFYVFLCFGVLYVKLGALSSVVALGANIICNKIPGLAPRQRAICQSRPDAII VIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVAHAVT AACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNARRLM NLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNVAVQVEV VRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNRTSPG ADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK NT seq 1050 nt NT seq  +upstreamnt  +downstreamnt atgcacagaaactttcgcaagtggattttctacgtgtttctctgctttggcgttctctac gtgaagctcggagcgctgtcatccgtcgtggccctgggagccaacatcatctgcaacaag attcctggcctggccccgcggcagcgcgccatctgtcagagccggcccgatgccatcatc gtgatcggggagggggcgcagatgggcatcaacgagtgccagtaccagttccgcttcggg cgctggaactgctccgccctcggcgagaagaccgtcttcggccaagagctccgagtaggg agccgtgaggccgccttcacctacgccatcaccgcggccggcgtggcccacgccgtcacc gccgcgtgcagccagggcaacctcagcaactgcggctgcgaccgcgagaagcagggctac tacaaccaggccgagggctggaagtggggcggctgctccgccgacgtgcgctatggcatc gacttctcccggcgcttcgtggacgcccgcgagatcaagaaaaacgcccggcgcctcatg aacttgcacaacaacgaggcgggcaggaaggtcctggaggagcgcatgaagctggagtgc aagtgccacggcgtgtcaggctcttgcaccaccaagacgtgctggaccacgctgcccaag ttccgcgaggtgggccacctgctgaaggagaagtacaacgtggctgtgcaggtcgaggtg gtgcgtgccagccgcctgcgccagcccaccttcctgcgcatcaagcagctgcgcagctac cagaagcccatggagacggacctggtgtacatcgagaagtcccccaactactgcgaggag gacgcggccacgggcagcgtgggcacgcagggccgcctgtgcaaccgcacgtcgcccggc gcagatggctgcgacaccatgtgctgcggccggggctacaacacccaccagtacaccaag gtctggcagtgcaattgcaagttccactggtgctgcttcgtcaagtgcaacacgtgcagc gagcgcaccgaggtcttcacctgcaagtga

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