Vulpes vulpes (red fox): 112910612 Help Entry 112910612         CDS       T05911                                  Symbol WNT16 Name (RefSeq) protein Wnt-16   KO K01558   wingless-type MMTV integration site family, member 16 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05202   Transcriptional misregulation in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112910612 (WNT16)    04390 Hippo signaling pathway     112910612 (WNT16)    04150 mTOR signaling pathway     112910612 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112910612 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112910612 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112910612 (WNT16)    05202 Transcriptional misregulation in cancer     112910612 (WNT16)    05205 Proteoglycans in cancer     112910612 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112910612 (WNT16)    05226 Gastric cancer     112910612 (WNT16)    05217 Basal cell carcinoma     112910612 (WNT16)    05224 Breast cancer     112910612 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112910612 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     112910612 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     112910612 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112910612 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:vvp00536]     112910612 (WNT16) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112910612 (WNT16) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  112910612 NCBI-ProteinID:  XP_025842602 LinkDB All DBs Position Unknown AA seq 302 aa AA seqDB search MRGRQPWKGPSAQPGACDPLAPHIPRDQKEDLLWTKPDRDTALSFSNLCFVLGTKETAFI YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL DFPIRNTTGKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE KVGRLLKDKYENSIQISDKIQRKVRRRDKDQRRVPIRKDDLLYVNKSPNYCVEDKKLGIP GTRGRECNRTSEGAGGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT CK NT seq 909 nt NT seq  +upstreamnt  +downstreamnt atgcgaggccgccagccctggaaaggtccatcggcccagcccggagcctgcgaccccctc gctcctcacatcccaagggaccaaaaggaagatttgttatggacaaaaccagacagagat acggctctttcattcagcaatttatgttttgttctaggcaccaaggaaacagcatttatt tatgctgtgatggctgcaggcctggtgcattctgtgaccaggtcatgcagtgccggcaac atgacggagtgctcctgtgacaccaccctacagaacggtggctcagcgagcgaaggctgg cactgggggggctgctctgatgatgtccagtatggcatgtggttcagcagaaagttccta gatttccccatcagaaacaccacaggaaaagaaagcaaagtactgttagcaatgaacctg cacaacaacgaagctggaaggcaggctgtcgccaagctcatgtcggtggactgccgctgt cacggggtctcgggctcctgcgccgtgaagacctgctggaaaaccatgtcctcgttcgag aaggtcggccggctgctgaaggacaagtacgaaaacagtatccagatctcagacaaaata cagcggaaggtgcgcaggagagacaaagaccagaggcgggtccccattcgcaaggacgac ctgctgtacgtcaacaagtcccccaactactgcgtggaggacaagaagctgggcatcccg ggcacgcggggccgcgagtgcaaccgcacctccgagggcgccggcggctgcaacctgctg tgctgcggccgcggctacaacacgcacgtggtcaggcacgtggagaggtgcgagtgcaag ttcatctggtgctgctacgttcgctgccggcgctgtgagagcatgaccgacgtgcacacc tgcaagtag

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