Physeter macrocephalus (sperm whale): 102985991 Help Entry 102985991         CDS       T06011                                  Symbol WNT7B Name (RefSeq) protein Wnt-7b   KO K00572   wingless-type MMTV integration site family, member 7 Organism pcad  Physeter macrocephalus (sperm whale) Pathway pcad04150   mTOR signaling pathway pcad04310   Wnt signaling pathway pcad04390   Hippo signaling pathway pcad04550   Signaling pathways regulating pluripotency of stem cells pcad04916   Melanogenesis pcad04934   Cushing syndrome pcad05010   Alzheimer disease pcad05022   Pathways of neurodegeneration - multiple diseases pcad05165   Human papillomavirus infection pcad05200   Pathways in cancer pcad05205   Proteoglycans in cancer pcad05217   Basal cell carcinoma pcad05224   Breast cancer pcad05225   Hepatocellular carcinoma pcad05226   Gastric cancer Brite KEGG Orthology (KO) [BR:pcad00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     102985991 (WNT7B)    04390 Hippo signaling pathway     102985991 (WNT7B)    04150 mTOR signaling pathway     102985991 (WNT7B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     102985991 (WNT7B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     102985991 (WNT7B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102985991 (WNT7B)    05205 Proteoglycans in cancer     102985991 (WNT7B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     102985991 (WNT7B)    05226 Gastric cancer     102985991 (WNT7B)    05217 Basal cell carcinoma     102985991 (WNT7B)    05224 Breast cancer     102985991 (WNT7B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     102985991 (WNT7B)   09164 Neurodegenerative disease    05010 Alzheimer disease     102985991 (WNT7B)    05022 Pathways of neurodegeneration - multiple diseases     102985991 (WNT7B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     102985991 (WNT7B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pcad00536]     102985991 (WNT7B) Glycosaminoglycan binding proteins [BR:pcad00536]  Heparan sulfate / Heparin   Morphogens    102985991 (WNT7B) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  102985991 NCBI-ProteinID:  XP_028347276 Ensembl:  ENSPCTG00005001409 UniProt:  A0A455BTU4 LinkDB All DBs Position 6:complement(48725863..48763025) Genome browser AA seq 369 aa AA seqDB search MSGVVGKAEVPAKPLGAETPSLAVGRALSSVVALGANIICNKIPGLAPRQRAICQSRPDA IIVIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVAHA VTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNARR LMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNVAVQV EVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNRTS PGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCKRGPCGPEWL KHWPETPRP NT seq 1110 nt NT seq  +upstreamnt  +downstreamnt atgtccggggtggtcgggaaggccgaagtgccggccaagccactaggcgccgagactccc agcctggccgtgggccgagcgctgtcatccgtcgtggccctgggagccaacatcatctgc aacaagatccctggcttggccccgcggcagcgtgccatctgccagagccggcccgatgcc atcatcgtgattggggagggggcgcagatgggcatcaacgagtgccagtaccagttccgc ttcggacgctggaactgctccgccctcggcgagaagactgtcttcgggcaagagctccga gtagggagccgtgaggccgccttcacatacgccatcaccgcagccggcgtggctcacgcc gtcaccgccgcctgcagccagggcaacctgagcaactgcgggtgcgaccgcgagaagcag ggctactacaaccaggccgagggctggaagtggggcggctgctccgccgacgtgcgctac ggcatcgacttctcccggcgcttcgtggacgcccgcgagatcaagaaaaacgcgaggcgc ctcatgaacctgcacaacaatgaggcgggcaggaaggtcctggaggagcgcatgaagctg gagtgcaagtgccacggcgtgtcaggctcgtgcaccaccaagacgtgctggaccacgctg cccaagttccgcgaggtgggccacctgctcaaggagaagtacaacgtggcggtgcaggtg gaggtggtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaagcagctgcgc agctaccagaagcccatggagacggacctggtgtacatcgagaagtcgcccaactactgc gaggaggacgcggccacgggcagcgtgggcacccagggccgcctgtgcaaccgcacctcg cccggcgccgacggctgcgacaccatgtgctgcggccgcggctacaacacccaccagtac accaaggtctggcagtgcaactgcaagttccactggtgctgcttcgtcaagtgcaacacg tgcagcgagcgcaccgaggtcttcacctgcaaacggggaccctgcggcccagaatggctc aagcactggccagagaccccaaggccgtga

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