Hylobates moloch (silvery gibbon): 116466764 Help Entry 116466764         CDS       T08803                                  Symbol WNT7A Name (RefSeq) protein Wnt-7a   KO K00572   wingless-type MMTV integration site family, member 7 Organism hmh  Hylobates moloch (silvery gibbon) Pathway hmh04150   mTOR signaling pathway hmh04310   Wnt signaling pathway hmh04390   Hippo signaling pathway hmh04550   Signaling pathways regulating pluripotency of stem cells hmh04916   Melanogenesis hmh04934   Cushing syndrome hmh05010   Alzheimer disease hmh05022   Pathways of neurodegeneration - multiple diseases hmh05165   Human papillomavirus infection hmh05200   Pathways in cancer hmh05205   Proteoglycans in cancer hmh05217   Basal cell carcinoma hmh05224   Breast cancer hmh05225   Hepatocellular carcinoma hmh05226   Gastric cancer Brite KEGG Orthology (KO) [BR:hmh00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     116466764 (WNT7A)    04390 Hippo signaling pathway     116466764 (WNT7A)    04150 mTOR signaling pathway     116466764 (WNT7A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     116466764 (WNT7A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     116466764 (WNT7A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     116466764 (WNT7A)    05205 Proteoglycans in cancer     116466764 (WNT7A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     116466764 (WNT7A)    05226 Gastric cancer     116466764 (WNT7A)    05217 Basal cell carcinoma     116466764 (WNT7A)    05224 Breast cancer     116466764 (WNT7A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     116466764 (WNT7A)   09164 Neurodegenerative disease    05010 Alzheimer disease     116466764 (WNT7A)    05022 Pathways of neurodegeneration - multiple diseases     116466764 (WNT7A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     116466764 (WNT7A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:hmh00536]     116466764 (WNT7A) Glycosaminoglycan binding proteins [BR:hmh00536]  Heparan sulfate / Heparin   Morphogens    116466764 (WNT7A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  116466764 NCBI-ProteinID:  XP_032005674 LinkDB All DBs Position Unknown AA seq 349 aa AA seqDB search MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEMYTCK NT seq 1050 nt NT seq  +upstreamnt  +downstreamnt atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac ctccggatcggcggcttctcctcagtggtagctctgggcgcaagcatcatctgtaacaag atcccaggcctggctcccagacagcgggcgatctgccagagccggcccgacgccatcatc gtcataggagaaggctcgcaaatgggcctggacgagtgtcagtttcagttccgcaatggc cgctggaactgctctgcactgggagagcgcaccgtctttgggaaggagctcaaagtgggg agccgggaggctgcattcacctacgccatcattgccgccggcgtggcccacgccatcaca gctgcctgtacccagggcaacctgagcgactgtggctgcgacaaagagaagcaaggccag taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg aacttgcacaataacgaggcaggccgaaagatcctggaggagaacatgaagctggaatgt aagtgccacggcgtgtcaggctcgtgcaccaccaagacgtgctggaccacactgccacag tttcgggagctaggctacgtgctcaaggacaagtacaacgaggccgttcacgtggagcct gtgcgtgccagccgcaacaagcggcccaccttcctgaagatcaagaagccactgtcgtac cgcaagcccatggacacggacctggtgtacatcgagaagtcgcccaactactgcgaggag gacccggtgaccggcagtgtgggcacccagggccgcgcctgcaacaagacggctccccag gccagcggctgtgacctcatgtgctgtgggcgtggctacaacacccaccagtacgcccgc gtgtggcagtgcaactgtaagttccactggtgctgctatgtcaagtgcaacacgtgcagc gagcgcacggagatgtacacgtgcaagtga

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