Mustela lutreola (European mink): 131829677 Help Entry 131829677         CDS       T09578                                  Symbol WNT16 Name (RefSeq) protein Wnt-16   KO K01558   wingless-type MMTV integration site family, member 16 Organism mlk  Mustela lutreola (European mink) Pathway mlk04150   mTOR signaling pathway mlk04310   Wnt signaling pathway mlk04390   Hippo signaling pathway mlk04550   Signaling pathways regulating pluripotency of stem cells mlk04916   Melanogenesis mlk04934   Cushing syndrome mlk05010   Alzheimer disease mlk05022   Pathways of neurodegeneration - multiple diseases mlk05165   Human papillomavirus infection mlk05200   Pathways in cancer mlk05202   Transcriptional misregulation in cancer mlk05205   Proteoglycans in cancer mlk05217   Basal cell carcinoma mlk05224   Breast cancer mlk05225   Hepatocellular carcinoma mlk05226   Gastric cancer Brite KEGG Orthology (KO) [BR:mlk00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     131829677 (WNT16)    04390 Hippo signaling pathway     131829677 (WNT16)    04150 mTOR signaling pathway     131829677 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     131829677 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     131829677 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     131829677 (WNT16)    05202 Transcriptional misregulation in cancer     131829677 (WNT16)    05205 Proteoglycans in cancer     131829677 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     131829677 (WNT16)    05226 Gastric cancer     131829677 (WNT16)    05217 Basal cell carcinoma     131829677 (WNT16)    05224 Breast cancer     131829677 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     131829677 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     131829677 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     131829677 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     131829677 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:mlk00536]     131829677 (WNT16) Glycosaminoglycan binding proteins [BR:mlk00536]  Heparan sulfate / Heparin   Morphogens    131829677 (WNT16) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  131829677 NCBI-ProteinID:  XP_059027670 LinkDB All DBs Position 4:173394199..173406129 Genome browser AA seq 362 aa AA seqDB search MDRAALLGLSRLCALWVALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC KKKPYLLPSIGEGARLGIQECRSQFRHERWNCLVTAAAPPGTSPLFGYELSSGTKETAFI YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL DFPIRNTTGKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE KIGHLLKDKYENSVQISDKIKRKMRRRDKDQRKIPIRKDDLLYVNKSPNYCVEDKKLGIP GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT CK NT seq 1089 nt NT seq  +upstreamnt  +downstreamnt atggacagagcggcgctcctgggactgtcgcgcctgtgcgcgctgtgggtagccctgctc gcgctgttcccctgcggagcccaaggaaattggatgtggttgggcatcgcctcctttggg gttccggagaagctgggctgcgccaacttgccgctgaacagccgccagaaggagctgtgc aagaagaaaccgtacctgctgccgagcatcggagagggcgcgcggctgggcattcaggag tgcaggagccagttcagacacgagaggtggaactgcctggtcaccgccgccgccccgccg ggcaccagccctctttttggctacgagctgagcagcggcaccaaggaaacagcatttatt tatgctgtgatggcagcaggcctggtgcattctgtgaccaggtcttgcagtgcaggcaac atgaccgagtgctcctgtgacaccaccttacagaacggcggttcagcaagcgaaggctgg cactgggggggctgctccgatgatgtccagtatggcatgtggttcagcagaaagttccta gatttccccatcagaaacactacaggaaaagaaagcaaagtacttttagcaatgaacctg cacaacaacgaagctggaaggcaggctgtcgccaagttgatgtccgtggattgccgatgt cacggagtttccggctcctgcgctgtgaaaacgtgctggaaaactatgtcttcttttgaa aagattggccacctgttgaaggataagtacgaaaacagtgtccaaatctcggacaaaata aagaggaaaatgcgcagaagagacaaagatcagaggaaaatacccattcgcaaggatgat ctcctctacgttaataagtctcccaattactgtgtcgaggataagaaactagggatcccc gggacccaaggcagagaatgcaaccgcacgtcggagggcgcggacggctgcaacctcctc tgctgtggccgaggctacaacacccacgtggtcaggcacgtggagaggtgcgagtgcaag tttatttggtgctgctacgtccgctgcaggaggtgtgaaagcatgactgacgtccacact tgcaagtag

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