WNT9B

Wingless-type MMTV integration site family, member 9B
Identifiers
Symbols	WNT9B ; WNT14B; WNT15
External IDs	OMIM: 602864 HomoloGene: 2551 GeneCards: WNT9B Gene
Gene ontology Molecular function • frizzled binding Cellular component • extracellular region • proteinaceous extracellular matrix • extracellular space Biological process • branching involved in ureteric bud morphogenesis • in utero embryonic development • regulation of protein phosphorylation • regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis • cell-cell signaling • multicellular organismal development • cellular response to starvation • regulation of asymmetric cell division • Wnt signaling pathway • neuron differentiation • male genitalia development • response to retinoic acid • regulation of tube size • positive regulation of catalytic activity • cell fate commitment • embryonic cranial skeleton morphogenesis • palate development • canonical Wnt signaling pathway • Wnt signaling pathway, planar cell polarity pathway • uterus morphogenesis • cornea development in camera-type eye • cellular response to retinoic acid • kidney rudiment formation • mesenchymal stem cell maintenance involved in nephron morphogenesis • collecting duct development • establishment of planar polarity involved in nephron morphogenesis • metanephric tubule formation • mesonephric duct formation Sources: Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	7484	22412
Ensembl	ENSG00000158955	ENSMUSG00000018486
UniProt	O14905	O35468
RefSeq (mRNA)	NM_003396	NM_011719
RefSeq (protein)	NP_003387	NP_035849
Location (UCSC)	Chr 17: 46.83 – 46.89 Mb	Chr 11: 103.73 – 103.75 Mb
PubMed search

Protein Wnt-9b (formerly Wnt15^[1]) is a protein that in humans is encoded by the WNT9B gene.^[2]

References

1. Garriock RJ, Warkman AS, Meadows SM, D'Agostino S, Krieg PA (2007). "Census of vertebrate Wnt genes: isolation and developmental expression of Xenopus Wnt2, Wnt3, Wnt9a, Wnt9b, Wnt10a, and Wnt16". Developmental Dynamics 236 (5): 1249–58. doi:10.1002/dvdy.21156. PMID 17436276.
2. "Entrez Gene: Wnt9b wingless-type MMTV integration site family, member 9B".