Pan paniscus (bonobo): 100995123 Help Entry 100995123         CDS       T02283                                  Symbol WNT10B Name (RefSeq) protein Wnt-10b   KO K01357   wingless-type MMTV integration site family, member 10 Organism pps  Pan paniscus (bonobo) Pathway pps04150   mTOR signaling pathway pps04310   Wnt signaling pathway pps04390   Hippo signaling pathway pps04519   Cadherin signaling 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 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     100995123 (WNT10B)    04390 Hippo signaling pathway     100995123 (WNT10B)    04150 mTOR signaling pathway     100995123 (WNT10B)   09133 Signaling molecules and interaction    04519 Cadherin signaling     100995123 (WNT10B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     100995123 (WNT10B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     100995123 (WNT10B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100995123 (WNT10B)    05205 Proteoglycans in cancer     100995123 (WNT10B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     100995123 (WNT10B)    05226 Gastric cancer     100995123 (WNT10B)    05217 Basal cell carcinoma     100995123 (WNT10B)    05224 Breast cancer     100995123 (WNT10B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     100995123 (WNT10B)   09164 Neurodegenerative disease    05010 Alzheimer disease     100995123 (WNT10B)    05022 Pathways of neurodegeneration - multiple diseases     100995123 (WNT10B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     100995123 (WNT10B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pps00536]     100995123 (WNT10B) Glycosaminoglycan binding proteins [BR:pps00536]  Heparan sulfate / Heparin   Morphogens    100995123 (WNT10B) SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  100995123 NCBI-ProteinID:  XP_003825867 Ensembl:  ENSPPAG00000035557 UniProt:  A0A2R9B5H3 LinkDB All DBs Position 10:45205454..45219702 Genome browser AA seq 389 aa AA seqDB search MLEEPRPRPPPSGLAGLLFLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLG LCLRNPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS FSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFPYSLPSP GPGSSPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLR PRRLSGELVYFEKSPDFCERDPTMGSPGTRGRACNKTSRLLDGCGSLCCGRGHNVLRQTR VERCHCRFHWCCYVLCDECKVTEWVNVCK NT seq 1170 nt NT seq  +upstreamnt  +downstreamnt atgctggaggagccccggccgcggcctccgccctcgggcctcgcgggtctcctgttcctg gcgttgtgcagtcgggctctaagcaatgagattctgggcctgaagttgcctggcgagccg ccgctgacggccaacaccgtgtgcttgacgctgtccggcctgagcaagcggcagctaggc ctgtgcctgcgcaaccccgacgtgacggcgtccgcgcttcagggtctgcacatcgcggtc cacgagtgtcagcaccagctgcgcgaccagcgctggaactgctccgcgcttgagggcggc ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgagaaagtgctttttcc ttctccatgctggctgctggggtcatgcacgcagtagccacggcctgcagcctgggcaag ctggtgagctgtggctgtggctggaagggcagtggtgagcaggatcggctgagggccaaa ctgctgcagctgcaggcactgtcccgaggcaagagtttcccctactctctgcccagccct ggccctggctcaagccccagccctggcccccaggacacatgggaatggggtggctgtaac catgacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc cgggacatccaggcacgaatgcgaatccacaacaacagggtggggcgccaggtggtaact gaaaacctgaagcggaaatgcaagtgtcatggcacgtcaggcagctgccagttcaagaca tgctggagggcggccccagagttccgggcagtgggggcggcgttgagggagcggctgggc cgggccatcttcattgatacccacaaccgcaattctggagccttccagccccgtctccgt ccccgtcgcctctcaggagagctggtctactttgagaagtctcctgacttctgtgagcga gaccccactatgggctccccagggacaaggggccgggcctgcaacaagaccagccgcctg ttggatggctgtggcagcctgtgctgtggccgtgggcacaacgtgctccggcagacacga gttgagcgctgccattgccgcttccactggtgctgctatgtgctgtgtgatgagtgcaag gttacagagtgggtgaatgtgtgtaagtga

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