Myotis davidii (David's myotis): 102773494 Help Entry 102773494         CDS       T02992                                  Symbol WNT16 Name (RefSeq) Wnt family member 16   KO K01558   wingless-type MMTV integration site family, member 16 Organism myd  Myotis davidii (David's myotis) Pathway myd04150   mTOR signaling pathway myd04310   Wnt signaling pathway myd04390   Hippo signaling pathway myd04550   Signaling pathways regulating pluripotency of stem cells myd04916   Melanogenesis myd04934   Cushing syndrome myd05010   Alzheimer disease myd05022   Pathways of neurodegeneration - multiple diseases myd05165   Human papillomavirus infection myd05200   Pathways in cancer myd05202   Transcriptional misregulation in cancer myd05205   Proteoglycans in cancer myd05217   Basal cell carcinoma myd05224   Breast cancer myd05225   Hepatocellular carcinoma myd05226   Gastric cancer Brite KEGG Orthology (KO) [BR:myd00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     102773494 (WNT16)    04390 Hippo signaling pathway     102773494 (WNT16)    04150 mTOR signaling pathway     102773494 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     102773494 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     102773494 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102773494 (WNT16)    05202 Transcriptional misregulation in cancer     102773494 (WNT16)    05205 Proteoglycans in cancer     102773494 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     102773494 (WNT16)    05226 Gastric cancer     102773494 (WNT16)    05217 Basal cell carcinoma     102773494 (WNT16)    05224 Breast cancer     102773494 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     102773494 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     102773494 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     102773494 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     102773494 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:myd00536]     102773494 (WNT16) Glycosaminoglycan binding proteins [BR:myd00536]  Heparan sulfate / Heparin   Morphogens    102773494 (WNT16) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  102773494 NCBI-ProteinID:  XP_015414957 LinkDB All DBs Position Un AA seq 299 aa AA seqDB search MGCPASDVHGGAAVSYRWLGIASFGVPEKLGCANXRLNSRQKDNLRLILGTKETAFIYAV MAAGLVHAVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWVSRKFLDFP IRNTTGRESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFEKIG HFLKDKYEHSVQVSDKIKRKMRRREKDQRKVPIRKEDLLYLHKSPNYCVEDKNIGIPGTQ GRECNRTSEGAGGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHTCK NT seq 900 nt NT seq  +upstreamnt  +downstreamnt atggggtgcccagcgagcgacgtgcatgggggggcggccgtttcttacaggtggttgggc atcgcctccttcggggtccccgagaagctgggctgcgccaactagcggctgaacagccgg cagaaggacaatttacgtcttattctaggcaccaaggaaacagcgtttatctacgcggtg atggctgcaggcctggtgcacgcggtgaccaggtcctgcagcgcaggcaacatgacggag tgctcctgtgacaccaccctgcagaacgggggctcagccagcgaaggctggcactggggg ggctgctcggatgacgtccagtacggcatgtgggtcagcagaaagttcctggacttcccc atcagaaacaccacgggcagagaaagcaaagtgctgttagcgatgaaccttcataacaac gaagctggaaggcaggctgtggccaagctgatgtccgtggactgccgctgtcacggcgtg tccggctcctgtgcggtgaaaacatgctggaaaaccatgtcttcatttgagaagattggc catttcctgaaggataaatatgagcacagtgttcaagtctcagacaaaataaaaaggaaa atgcgcaggagagaaaaggaccagaggaaagtaccgatccgcaaggaggatctgctctac ctccataagtctcccaactactgcgtagaggataagaacattgggatcccggggacgcag ggcagagaatgcaaccgcacgtcggagggcgcgggtggctgcaacctcctctgctgtggc cgaggctacaacacacacgtggtcagacacgtggagaggtgcgagtgcaagttcatctgg tgctgctacgttcgctgcaggaggtgtgaaagcatgactgacgtccacacctgcaagtaa

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