Pongo abelii (Sumatran orangutan): 100452466 Help Entry 100452466         CDS       T01416                                  Symbol WNT16 Name (RefSeq) protein Wnt-16   KO K01558   wingless-type MMTV integration site family, member 16 Organism pon  Pongo abelii (Sumatran orangutan) Pathway pon04150   mTOR signaling pathway pon04310   Wnt signaling pathway pon04390   Hippo signaling pathway pon04550   Signaling pathways regulating pluripotency of stem cells pon04916   Melanogenesis pon04934   Cushing syndrome pon05010   Alzheimer disease pon05022   Pathways of neurodegeneration - multiple diseases pon05165   Human papillomavirus infection pon05200   Pathways in cancer pon05202   Transcriptional misregulation in cancer pon05205   Proteoglycans in cancer pon05217   Basal cell carcinoma pon05224   Breast cancer pon05225   Hepatocellular carcinoma pon05226   Gastric cancer Brite KEGG Orthology (KO) [BR:pon00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     100452466 (WNT16)    04390 Hippo signaling pathway     100452466 (WNT16)    04150 mTOR signaling pathway     100452466 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100452466 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100452466 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100452466 (WNT16)    05202 Transcriptional misregulation in cancer     100452466 (WNT16)    05205 Proteoglycans in cancer     100452466 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100452466 (WNT16)    05226 Gastric cancer     100452466 (WNT16)    05217 Basal cell carcinoma     100452466 (WNT16)    05224 Breast cancer     100452466 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100452466 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     100452466 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     100452466 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100452466 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pon00536]     100452466 (WNT16) Glycosaminoglycan binding proteins [BR:pon00536]  Heparan sulfate / Heparin   Morphogens    100452466 (WNT16) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  100452466 NCBI-ProteinID:  XP_002818419 Ensembl:  ENSPPYG00000017947 UniProt:  H2PNB7 LinkDB All DBs Position 6:118615020..118627085 Genome browser AA seq 365 aa AA seqDB search MDRAALLGLARLCALWAALLVLFPYGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC KRKPYLLPSIREGARLGIQECRNQFRHERWNCMITAAATTAPMGASPLFGYELSSGTKET AFIYAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSR KFLDFPIGNTTGKENKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMS SFEKIGHLLKDKYENSIQISDKIKRKMRRREKDQRKIPIHKDDLLYVNKSPNYCVEDKKL GIPGTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTD VHTCK NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atggacagggcggcgctcctgggactggcccgcttgtgcgcgctgtgggcagccctgctc gtgctgttcccctacggagcccaaggaaactggatgtggttgggcattgcctccttcggg gttccagagaagctgggctgcgccaatttgccgctgaacagccgccagaaggagctgtgc aagaggaaaccgtacctgctgccgagcatccgggagggcgcccggctgggcattcaggag tgcaggaaccagttcagacacgagagatggaactgcatgatcaccgccgccgccaccacc gccccgatgggcgccagccccctctttggctacgagctgagcagcggcaccaaagagaca gcatttatttatgctgtgatggctgcaggcctggtgcattctgtgaccaggtcatgcagt gcaggcaacatgacagagtgttcctgtgacaccaccttgcagaacggcggctcagcaagt gaaggctggcactgggggggctgctctgatgatgtccagtatggcatgtggttcagcaga aagttcctagatttccccattggaaacaccacgggcaaagaaaacaaagtactattagca atgaacctacataacaatgaagctggaaggcaggctgtcgccaagttgatgtcagtagac tgccgctgccacggagtttccggctcctgtgctgtgaaaacatgctggaaaaccatgtct tcttttgaaaagattggccatttgttgaaggataaatatgaaaacagtatccagatatca gacaaaataaagaggaaaatgcgcaggagagaaaaagatcagaggaaaataccaatccac aaggatgatctgctctatgttaataagtctcccaactactgtgtagaagataagaaactg ggaatcccagggacacaaggcagagagtgcaaccgtacatcagagggtgcagatggctgc aacctcctctgctgtggccgaggttacaacacccacgtggtcaggcacgtggagaggtgt gagtgtaagttcatctggtgctgctatgtccgttgcaggaggtgtgaaagcatgactgat gtccacacttgcaagtaa

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