Pteropus vampyrus (large flying fox): 105294978 Help Entry 105294978         CDS       T07815                                  Symbol WNT7A Name (RefSeq) protein Wnt-7a   KO K00572   wingless-type MMTV integration site family, member 7 Organism pvp  Pteropus vampyrus (large flying fox) Pathway pvp04150   mTOR signaling pathway pvp04310   Wnt signaling pathway pvp04390   Hippo signaling pathway pvp04550   Signaling pathways regulating pluripotency of stem cells pvp04916   Melanogenesis pvp04934   Cushing syndrome pvp05010   Alzheimer disease pvp05022   Pathways of neurodegeneration - multiple diseases pvp05165   Human papillomavirus infection pvp05200   Pathways in cancer pvp05205   Proteoglycans in cancer pvp05217   Basal cell carcinoma pvp05224   Breast cancer pvp05225   Hepatocellular carcinoma pvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:pvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     105294978 (WNT7A)    04390 Hippo signaling pathway     105294978 (WNT7A)    04150 mTOR signaling pathway     105294978 (WNT7A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     105294978 (WNT7A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     105294978 (WNT7A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     105294978 (WNT7A)    05205 Proteoglycans in cancer     105294978 (WNT7A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     105294978 (WNT7A)    05226 Gastric cancer     105294978 (WNT7A)    05217 Basal cell carcinoma     105294978 (WNT7A)    05224 Breast cancer     105294978 (WNT7A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     105294978 (WNT7A)   09164 Neurodegenerative disease    05010 Alzheimer disease     105294978 (WNT7A)    05022 Pathways of neurodegeneration - multiple diseases     105294978 (WNT7A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     105294978 (WNT7A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pvp00536]     105294978 (WNT7A) Glycosaminoglycan binding proteins [BR:pvp00536]  Heparan sulfate / Heparin   Morphogens    105294978 (WNT7A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  105294978 NCBI-ProteinID:  XP_011362760 UniProt:  A0A6P3QT62 LinkDB All DBs Position Unknown AA seq 349 aa AA seqDB search MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEVYTCK NT seq 1050 nt NT seq  +upstreamnt  +downstreamnt atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac ctccggatcggtggcttctcctcggtggtagctctgggcgcgagcatcatctgtaacaag atcccaggcctggctcccagacagcgggcgatctgccagagccggcccgacgccatcatc gtcataggagaaggctcacaaatgggcctcgacgagtgtcagtttcagttccgcaatggc cgctggaactgctccgcgctgggggagcgcaccgtcttcggaaaggagctcaaagtgggg agccgagaggctgccttcacgtatgccatcattgctgccggtgtggcccatgccatcaca gctgcctgtacccagggcaacctgagtgactgtggctgcgacaaggagaagcaaggccag taccaccgggacgagggctggaagtggggtggctgctctgccgacattcgctacggcatc ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg aacttacacaataacgaggcaggccgaaagatcctggaagagaacatgaagctggagtgt aagtgccatggcgtgtcagggtcatgcaccaccaagacgtgctggaccacactgccacag ttccgggagctgggctatgtgctcaaggacaagtacaatgaggctgttcacgtggagcct gtacgcgctagccgcaacaagcggcccaccttcctgaagatcaagaagccactgtcatac cgcaagcccatggacacagacctggtgtacatcgagaagtcacccaactactgtgaggag gacccagtgaccggtagtgtgggcacgcagggccgcgcctgcaacaagacagccccccaa gccagtggttgtgacctcatgtgctgtggccgtggctacaacacccaccagtatgcccgc gtgtggcagtgcaactgcaaattccactggtgctgctatgtcaagtgcaacacctgcagt gaacgcacggaagtgtatacgtgcaagtga

DBGET integrated database retrieval system