Myotis yumanensis (Yuma myotis): 139002969 Help Entry 139002969         CDS       T10762                                  Symbol WNT4 Name (RefSeq) protein Wnt-4 isoform X1   KO K00408   wingless-type MMTV integration site family, member 4 Organism myum  Myotis yumanensis (Yuma myotis) Pathway myum04150   mTOR signaling pathway myum04310   Wnt signaling pathway myum04360   Axon guidance myum04390   Hippo signaling pathway myum04550   Signaling pathways regulating pluripotency of stem cells myum04916   Melanogenesis myum04919   Thyroid hormone signaling pathway myum04934   Cushing syndrome myum05010   Alzheimer disease myum05022   Pathways of neurodegeneration - multiple diseases myum05165   Human papillomavirus infection myum05200   Pathways in cancer myum05205   Proteoglycans in cancer myum05217   Basal cell carcinoma myum05224   Breast cancer myum05225   Hepatocellular carcinoma myum05226   Gastric cancer Brite KEGG Orthology (KO) [BR:myum00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     139002969 (WNT4)    04390 Hippo signaling pathway     139002969 (WNT4)    04150 mTOR signaling pathway     139002969 (WNT4)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     139002969 (WNT4)  09150 Organismal Systems   09152 Endocrine system    04919 Thyroid hormone signaling pathway     139002969 (WNT4)    04916 Melanogenesis     139002969 (WNT4)   09158 Development and regeneration    04360 Axon guidance     139002969 (WNT4)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     139002969 (WNT4)    05205 Proteoglycans in cancer     139002969 (WNT4)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     139002969 (WNT4)    05226 Gastric cancer     139002969 (WNT4)    05217 Basal cell carcinoma     139002969 (WNT4)    05224 Breast cancer     139002969 (WNT4)   09172 Infectious disease: viral    05165 Human papillomavirus infection     139002969 (WNT4)   09164 Neurodegenerative disease    05010 Alzheimer disease     139002969 (WNT4)    05022 Pathways of neurodegeneration - multiple diseases     139002969 (WNT4)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     139002969 (WNT4)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:myum00536]     139002969 (WNT4) Glycosaminoglycan binding proteins [BR:myum00536]  Heparan sulfate / Heparin   Morphogens    139002969 (WNT4) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  139002969 NCBI-ProteinID:  XP_070260404 LinkDB All DBs Position Unknown AA seq 351 aa AA seqDB search MSPRSCLRSLRLLVFAVFSAAASNWLYLAKLSSVGSISEEETCEKLKGLIQRQVQMCKRN LEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAISSAGV AFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRERSKGAS SSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALKEKFDG ATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDMRSGVLGTRGRTCNKTS KAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR NT seq 1056 nt NT seq  +upstreamnt  +downstreamnt atgagtccccgctcctgcctgcgttcgctgcgcctcctcgtcttcgccgtcttctcggcc gccgcgagcaactggctgtacctggccaagctgtcctcggtggggagcatctcggaggag gagacctgcgagaagctcaagggcctgatccagcggcaggtgcagatgtgcaagcggaat ctggaggtgatggactcggtgcgccgcggcgcccagctcgccatcgaggagtgccagtac cagttccggaaccggcgctggaactgctccacgctcgactccctgcccgtcttcggcaag gtggtgacgcaagggactcgggaggcggccttcgtgtacgccatctcttcagcaggtgtg gccttcgcggtgacgcgggcgtgcagcagtggggagctggaaaagtgcggctgtgaccgg acagtacacggggtcagcccccagggcttccagtggtcaggatgctccgacaacatcgcc tatggcgtggccttctcacagtcgttcgtggacgtgcgggagaggagcaagggggcctcg tctagccgggccctcatgaacctccacaacaatgaggccggcaggaaggccatcctgacg cacatgcgggtggagtgcaagtgccacggggtgtcgggctcctgtgaggtaaagacctgc tggcgagccgtgccgcccttccgccaggtgggccacgccctgaaggagaagtttgacggt gccaccgaggtggagccgcggcgtgtgggctcctccagggcgctggtgccgcgcaacgcg cagttcaagccgcacaccgacgaggacctggtgtacttggagcccagcccggacttctgc gagcaggacatgcgcagcggggtgctgggcacgcggggccgcacgtgcaacaagacatcc aaggccatcgacggctgtgagctgctgtgctgcggccgcggcttccacacggcacaggtg gagctggccgagcgctgcagctgcaagttccactggtgctgcttcgtcaagtgccggcag tgccagcggctggtggagctgcacacgtgccggtga

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