Puma concolor (puma): 112867003 Help Entry 112867003         CDS       T08890                                  Symbol WNT16 Name (RefSeq) protein Wnt-16   KO K01558   wingless-type MMTV integration site family, member 16 Organism pcoo  Puma concolor (puma) Pathway pcoo04150   mTOR signaling pathway pcoo04310   Wnt signaling pathway pcoo04390   Hippo signaling pathway pcoo04550   Signaling pathways regulating pluripotency of stem cells pcoo04916   Melanogenesis pcoo04934   Cushing syndrome pcoo05010   Alzheimer disease pcoo05022   Pathways of neurodegeneration - multiple diseases pcoo05165   Human papillomavirus infection pcoo05200   Pathways in cancer pcoo05202   Transcriptional misregulation in cancer pcoo05205   Proteoglycans in cancer pcoo05217   Basal cell carcinoma pcoo05224   Breast cancer pcoo05225   Hepatocellular carcinoma pcoo05226   Gastric cancer Brite KEGG Orthology (KO) [BR:pcoo00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112867003 (WNT16)    04390 Hippo signaling pathway     112867003 (WNT16)    04150 mTOR signaling pathway     112867003 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112867003 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112867003 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112867003 (WNT16)    05202 Transcriptional misregulation in cancer     112867003 (WNT16)    05205 Proteoglycans in cancer     112867003 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112867003 (WNT16)    05226 Gastric cancer     112867003 (WNT16)    05217 Basal cell carcinoma     112867003 (WNT16)    05224 Breast cancer     112867003 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112867003 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     112867003 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     112867003 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112867003 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pcoo00536]     112867003 (WNT16) Glycosaminoglycan binding proteins [BR:pcoo00536]  Heparan sulfate / Heparin   Morphogens    112867003 (WNT16) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  112867003 NCBI-ProteinID:  XP_025785752 UniProt:  A0A6P6IC78 LinkDB All DBs Position Unknown AA seq 362 aa AA seqDB search MDRAALLGLSRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC KRKPYLLPSIGEGARLGIQECRSQFRHERWNCLVTATAQPGTSPLFGYELSSGTKETAFI YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL DFPIQNTTGKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE KIGHLLKDKYENSIQISDKIKRKMRRREKDQRKIPIRKDDLLYLNKSPNYCVEDKKLGIP GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT CK NT seq 1089 nt NT seq  +upstreamnt  +downstreamnt atggacagagcggcgctcctgggactgtcccgcctgtgcgcgctgtgggcagccctgctc gcgctgttcccctgcggagcccaaggaaattggatgtggttgggcatcgcttcctttggg gttccggagaagctgggctgcgccaacttgccgctgaacagccgccagaaggagctgtgc aagaggaaaccgtacctgctgccgagcatcggagagggcgcgcggctgggcattcaggag tgcaggagccagttcagacacgagagatggaactgcctggtcaccgccaccgcccagccg ggcaccagccccctctttggctacgagctgagcagcggcaccaaggaaacagcatttatt tatgctgtgatggctgcaggcctggtgcattctgtgaccaggtcatgcagtgcaggcaac atgaccgagtgctcctgtgacaccaccttgcagaatggcggctcagctagtgaaggctgg cactgggggggctgctccgatgatgtccagtatggcatgtggttcagcagaaagttccta gatttccccatccaaaacaccacaggaaaagaaagcaaagttctgttagcgatgaaccta cacaacaatgaagccggaaggcaggccgtcgccaagctgatgtcagtagactgtcgctgc cacggagtgtccggctcctgcgctgtgaaaacgtgctggaaaacgatgtcttcctttgaa aagatcggccatttgttgaaggacaaatatgaaaacagtatccaaatctcagacaaaata aagaggaaaatgcgcaggagagaaaaagatcagaggaagatacccatccgcaaagatgat ctgctctaccttaataagtctcccaattactgtgtagaggacaagaaactagggatccca ggaacacagggcagagaatgcaaccgcacgtcagagggcgcggacggctgcaacctcctt tgttgtggccgcggctacaacacccacgtggtcaggcacgtggagaggtgcgagtgcaag ttcatctggtgctgctacgtccgctgcaggaggtgtgaaagcatgactgacgtccacact tgcaagtag

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