Pan paniscus (bonobo): 100985948 Help Entry 100985948         CDS       T02283                                  Symbol WNT16 Name (RefSeq) protein Wnt-16 isoform X1   KO K01558   wingless-type MMTV integration site family, member 16 Organism pps  Pan paniscus (bonobo) Pathway pps04150   mTOR signaling pathway pps04310   Wnt signaling pathway pps04390   Hippo signaling pathway pps04550   Signaling pathways regulating pluripotency of stem cells pps04916   Melanogenesis pps04934   Cushing syndrome pps05010   Alzheimer disease pps05022   Pathways of neurodegeneration - multiple diseases pps05165   Human papillomavirus infection pps05200   Pathways in cancer pps05202   Transcriptional misregulation in cancer pps05205   Proteoglycans in cancer pps05217   Basal cell carcinoma pps05224   Breast cancer pps05225   Hepatocellular carcinoma pps05226   Gastric cancer Brite KEGG Orthology (KO) [BR:pps00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100985948 (WNT16)    04390 Hippo signaling pathway     100985948 (WNT16)    04150 mTOR signaling pathway     100985948 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100985948 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100985948 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100985948 (WNT16)    05202 Transcriptional misregulation in cancer     100985948 (WNT16)    05205 Proteoglycans in cancer     100985948 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100985948 (WNT16)    05226 Gastric cancer     100985948 (WNT16)    05217 Basal cell carcinoma     100985948 (WNT16)    05224 Breast cancer     100985948 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100985948 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     100985948 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     100985948 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100985948 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pps00536]     100985948 (WNT16) Glycosaminoglycan binding proteins [BR:pps00536]  Heparan sulfate / Heparin   Morphogens    100985948 (WNT16) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  100985948 NCBI-ProteinID:  XP_003808686 Ensembl:  ENSPPAG00000028372 UniProt:  A0A2R8ZZ85 LinkDB All DBs Position 6:158199273..158223862 Genome browser AA seq 365 aa AA seqDB search MDRAALLGLARLCALWAALLVLFPYGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC KRKPYLLPSIREGARLGIQECRSQFRHERWNCMITAAATTAPMGASPLFGYELSSGTKET AFIYAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSR KFLDFPIGNTTGKENKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMS SFEKIGHLLKDKYENSIQISDKIKRKMRRREKDQRKTPIHKDDLLYVNKSPNYCVEDKKL GIPGTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTD VHTCK NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atggacagggcggcgctcctgggactggcccgcttgtgcgcgctgtgggcagcccttctc gtgctgttcccctacggagcccaaggaaactggatgtggttgggcattgcctccttcggg gttccagagaagctgggctgcgccaatttgccgctgaacagtcgccagaaggagctgtgc aagaggaaaccgtacctgctgccgagcatccgagagggcgcccggctgggcattcaggag tgcaggagccagttcagacacgagagatggaactgcatgatcaccgccgccgccaccacc gccccgatgggcgccagccccctctttggctacgagctgagcagcggcaccaaagagaca gcatttatttatgctgtgatggctgcaggcctggtgcattctgtgaccaggtcatgcagt gcaggcaacatgacagagtgttcctgtgacaccaccttgcagaacggcggctcagcaagt gaaggctggcactgggggggctgctccgatgatgtccagtatggcatgtggttcagcaga aagttcctggatttccccatcggaaacaccacgggcaaagaaaacaaagtactattagca atgaacctacataacaatgaagctggaaggcaggctgtcgccaagctgatgtcagtagac tgccgctgccacggagtttccggctcctgtgctgtgaaaacatgctggaaaaccatgtct tcttttgaaaagattggccatttgttgaaggataaatatgaaaacagtatccagatatca gacaaaataaagaggaaaatgcgcaggagagaaaaagatcagaggaaaacaccaatccac aaggatgatctgctctatgttaataagtctcccaactactgtgtagaagataagaaactg ggaatcccagggacacaaggcagagaatgcaaccgtacatcagagggtgcagatggctgc aacctcctctgctgtggccgaggttacaacacccatgtggtcaggcacgtggagaggtgt gagtgtaagttcatctggtgctgctatgtccgttgcaggaggtgtgaaagcatgactgat gtccacacttgcaagtaa

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