Neogale vison (American mink): 122905021 Help Entry 122905021         CDS       T08764                                  Symbol WNT16 Name (RefSeq) protein Wnt-16   KO K01558   wingless-type MMTV integration site family, member 16 Organism nvs  Neogale vison (American mink) Pathway nvs04150   mTOR signaling pathway nvs04310   Wnt signaling pathway nvs04390   Hippo signaling pathway nvs04550   Signaling pathways regulating pluripotency of stem cells nvs04916   Melanogenesis nvs04934   Cushing syndrome nvs05010   Alzheimer disease nvs05022   Pathways of neurodegeneration - multiple diseases nvs05165   Human papillomavirus infection nvs05200   Pathways in cancer nvs05202   Transcriptional misregulation in cancer nvs05205   Proteoglycans in cancer nvs05217   Basal cell carcinoma nvs05224   Breast cancer nvs05225   Hepatocellular carcinoma nvs05226   Gastric cancer Brite KEGG Orthology (KO) [BR:nvs00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     122905021 (WNT16)    04390 Hippo signaling pathway     122905021 (WNT16)    04150 mTOR signaling pathway     122905021 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     122905021 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     122905021 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     122905021 (WNT16)    05202 Transcriptional misregulation in cancer     122905021 (WNT16)    05205 Proteoglycans in cancer     122905021 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     122905021 (WNT16)    05226 Gastric cancer     122905021 (WNT16)    05217 Basal cell carcinoma     122905021 (WNT16)    05224 Breast cancer     122905021 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     122905021 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     122905021 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     122905021 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     122905021 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:nvs00536]     122905021 (WNT16) Glycosaminoglycan binding proteins [BR:nvs00536]  Heparan sulfate / Heparin   Morphogens    122905021 (WNT16) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  122905021 NCBI-ProteinID:  XP_044102388 UniProt:  A0A8C7A721 LinkDB All DBs Position 4:202271933..202285830 Genome browser AA seq 362 aa AA seqDB search MDRAALLGLSRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC KKKPYLLPSIGEGARLGIQECRSQFRHERWNCLVTAAATPGTSPLFGYELSSGTKETAFI YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL DFPIRNTTGKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE KIGHLLKDKYENSVQISDKIKRKMRRRDKDQRKIPIGKDELLYVNKSPNYCVEDKKRGIP GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT CK NT seq 1089 nt NT seq  +upstreamnt  +downstreamnt atggacagagcggcgctcctgggactgtcgcgcctgtgcgcgctgtgggcagccctgctc gcgctgttcccctgcggagcccaaggaaattggatgtggttgggcatcgcctcctttggg gttccggagaagctgggctgcgccaacttgccgctgaacagccgccagaaggagctgtgc aagaagaaaccgtacctgctgccgagcatcggagagggcgcgcggctgggcattcaggag tgcaggagccagttcagacacgagaggtggaactgcctggtcaccgccgccgccacgccg ggcaccagccccctttttggctacgagctgagcagcggcaccaaggaaacagcatttatt tatgctgtgatggcagcaggcctggtgcattctgtgaccaggtcttgcagtgcaggcaac atgaccgagtgctcctgtgacaccaccttacagaacggcggttcagcaagcgaaggctgg cactgggggggctgctcagatgatgtccagtatggcatgtggttcagcagaaagttccta gatttccccatcagaaacactacaggaaaagaaagcaaagtacttttagcaatgaacctg cacaacaacgaagctggaaggcaggctgtcgccaagttgatgtccgtggattgccgatgt cacggagtttccggctcctgcgctgtgaaaacgtgctggaaaactatgtcttctttcgaa aagattggccacttgttgaaggataagtacgaaaacagtgtccaaatctccgacaaaata aagaggaaaatgcgcagaagagacaaagatcagaggaaaatacccattggcaaggatgaa ctcctctacgttaataagtctcccaattactgcgtcgaggataagaaacgagggatcccc gggacccaaggcagagaatgcaaccgcacgtcggagggcgcggacggctgcaacctcctt tgctgcggccgaggctacaacacccacgtggtcaggcacgtggagaggtgcgagtgcaag tttatttggtgctgctacgtccgctgcaggaggtgtgaaagcatgactgacgtccacact tgcaagtag

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