Mustela putorius furo (domestic ferret): 101692294 Help Entry 101692294         CDS       T07239                                  Symbol WNT16 Name (RefSeq) protein Wnt-16   KO K01558   wingless-type MMTV integration site family, member 16 Organism mpuf  Mustela putorius furo (domestic ferret) Pathway mpuf04150   mTOR signaling pathway mpuf04310   Wnt signaling pathway mpuf04390   Hippo signaling pathway mpuf04550   Signaling pathways regulating pluripotency of stem cells mpuf04916   Melanogenesis mpuf04934   Cushing syndrome mpuf05010   Alzheimer disease mpuf05022   Pathways of neurodegeneration - multiple diseases mpuf05165   Human papillomavirus infection mpuf05200   Pathways in cancer mpuf05202   Transcriptional misregulation in cancer mpuf05205   Proteoglycans in cancer mpuf05217   Basal cell carcinoma mpuf05224   Breast cancer mpuf05225   Hepatocellular carcinoma mpuf05226   Gastric cancer Brite KEGG Orthology (KO) [BR:mpuf00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     101692294 (WNT16)    04390 Hippo signaling pathway     101692294 (WNT16)    04150 mTOR signaling pathway     101692294 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     101692294 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     101692294 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     101692294 (WNT16)    05202 Transcriptional misregulation in cancer     101692294 (WNT16)    05205 Proteoglycans in cancer     101692294 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     101692294 (WNT16)    05226 Gastric cancer     101692294 (WNT16)    05217 Basal cell carcinoma     101692294 (WNT16)    05224 Breast cancer     101692294 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     101692294 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     101692294 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     101692294 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     101692294 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:mpuf00536]     101692294 (WNT16) Glycosaminoglycan binding proteins [BR:mpuf00536]  Heparan sulfate / Heparin   Morphogens    101692294 (WNT16) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  101692294 NCBI-ProteinID:  XP_004741947 Ensembl:  ENSMPUG00000006909 UniProt:  A0A8U0SQK4 M3Y6A3 LinkDB All DBs Position Unknown AA seq 362 aa AA seqDB search MDRAALLGLSRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC KKKPYLLPSIGEGARLGIQECRSQFRHERWNCLVAAAAPPGTSPLFGYELSSGTKETAFI YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL DFPIRNTTGKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE KIGHLLKDKYENSVQISDKIKRKMRRRDKDQRKIPIRKDDLLYVNKSPNYCVEDKKLGIP GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT CK NT seq 1089 nt NT seq  +upstreamnt  +downstreamnt atggacagagcggcgctcctgggactgtcgcgcctgtgcgcgctgtgggcagccctgctc gcgctgttcccctgcggagcccaaggaaattggatgtggttgggcatcgcctcctttggg gttccggagaagctgggctgcgccaacttgccgctgaacagccgccagaaggagctgtgc aagaagaaaccgtacctgctgccgagcatcggagagggcgcgcggctgggcattcaggag tgcaggagccagttcagacacgagaggtggaactgcctggtcgccgccgccgccccgccg ggcaccagccctctttttggctacgagctgagcagcggcacaaaggaaacagcatttatt tatgctgtgatggcagcaggcctggtgcattctgtgaccaggtcttgcagtgcaggcaac atgaccgagtgctcctgtgacaccaccttacagaacggcggttcagcaagcgaaggctgg cactgggggggctgctccgatgatgtccagtatggcatgtggttcagcagaaagttccta gatttccccatcagaaacactacaggaaaagaaagcaaagtacttttagcaatgaacctg cacaacaacgaagctggaaggcaggctgtcgccaagttgatgtccgtggattgccgatgt cacggagtttccggctcctgcgctgtgaaaacgtgctggaaaactatgtcttcttttgaa aagattggccacctgttgaaggataagtacgaaaacagtgtccaaatctcggacaaaata aagaggaaaatgcgcagaagagacaaagatcagaggaaaatacccattcgcaaggatgat ctcctctacgttaataagtctcccaattactgtgtcgaggataagaaactagggatcccc gggacccaaggcagagaatgcaaccgcacgtcggagggcgcggacggctgcaacctcctc tgctgtggccgaggctacaacacccacgtggtcaggcacgtggagaggtgcgagtgcaag tttatttggtgctgctacgtccgctgcaggaggtgtgaaagcatgactgacgtccacact tgcaagtag

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