Myotis davidii (David's myotis): 102758435 Help Entry 102758435         CDS       T02992                                  Symbol WNT8B Name (RefSeq) Wnt family member 8B   KO K00714   wingless-type MMTV integration site family, member 8 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 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     102758435 (WNT8B)    04390 Hippo signaling pathway     102758435 (WNT8B)    04150 mTOR signaling pathway     102758435 (WNT8B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     102758435 (WNT8B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     102758435 (WNT8B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102758435 (WNT8B)    05205 Proteoglycans in cancer     102758435 (WNT8B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     102758435 (WNT8B)    05226 Gastric cancer     102758435 (WNT8B)    05217 Basal cell carcinoma     102758435 (WNT8B)    05224 Breast cancer     102758435 (WNT8B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     102758435 (WNT8B)   09164 Neurodegenerative disease    05010 Alzheimer disease     102758435 (WNT8B)    05022 Pathways of neurodegeneration - multiple diseases     102758435 (WNT8B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     102758435 (WNT8B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:myd00536]     102758435 (WNT8B) Glycosaminoglycan binding proteins [BR:myd00536]  Heparan sulfate / Heparin   Morphogens    102758435 (WNT8B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  102758435 NCBI-ProteinID:  XP_015414763 LinkDB All DBs Position Un AA seq 300 aa AA seqDB search MLLMKPSVCIFLLTCVLHLSHTWXVNNICILTPVSPKAYLIYSSSVAAGAQSGIEECKYQ FAWDRWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDS RNGQLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMK RTCKCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADT FRSISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRFCSRAERPRGGAAHKPARKP NT seq 903 nt NT seq  +upstreamnt  +downstreamnt atgttacttatgaagccttctgtgtgcatctttcttctcacctgcgtcctccacctcagc catacctggtaagtaaataacatctgcattttgacccctgtgtccccgaaggcttacctg atctactccagcagtgtggccgctggtgcccagagcgggattgaagaatgcaaataccag ttcgcctgggaccgctggaactgccctgagagagccctgcagctgtccagccatggcggc ctgcgcagtgctaaccgggagacagccttcgtacacgccatcagttctgccggcgtcatg tacactctgactcggaactgtagccttggggattttgacaactgtggctgtgatgactcc cgcaacgggcagctggggggccaaggctggctgtggggaggctgcagtgacaacgtgggc ttcggagaggcaatatccaagcagttcgttgatgccctggagaccggacaggatgcccgg gcagccatgaacttgcacaacaatgaggccggccgcaaggcggtgaagggcaccatgaaa cgcacgtgtaagtgccacggcgtgtctggcagctgcaccacgcagacctgctggctgcag ctgccggagttccgcgaggtgggcgcgcacctgaaggagaagtaccacgcagctctcaag gtggacctgctgcaaggtgctggcaacagcgcggccggacgcggcgccatcgccgacacc tttcgctccatctccacgcgggagctggtgcacttggaggactccccagactactgcctg gagaacaaaacgctaggcctgctgggcacggagggccgagagtgcctgcggcgcgggcgc ttctgcagccgcgcggagcggccgcgggggggcgctgcgcacaaacccgcgagaaaaccc taa

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