WNT9B

WNT9B
Identifiers
Aliases	WNT9B, WNT14B, WNT15, Wnt family member 9B
External IDs	MGI: 1197020 HomoloGene: 2551 GeneCards: WNT9B
Genetically Related Diseases
vasculitis[1]
Gene ontology Molecular function • frizzled binding • receptor binding • co-receptor binding Cellular component • proteinaceous extracellular matrix • extracellular fluid • extracellular region Biological process • kidney morphogenesis • cell-cell signaling • cellular response to starvation • mesonephric duct formation • canonical Wnt signaling pathway • multicellular organism development • male genitalia development • cornea development in camera-type eye • branching morphogenesis of an epithelial tube • kidney rudiment formation • collecting duct development • regulation of asymmetric cell division • embryonic cranial skeleton morphogenesis • kidney development • Wnt signaling pathway, planar cell polarity pathway • cellular response to retinoic acid • mesenchymal stem cell maintenance involved in nephron morphogenesis • establishment of planar polarity involved in nephron morphogenesis • nephron tubule morphogenesis • palate development • metanephric tubule development • in utero embryonic development • regulation of tube size • mesonephric tubule development • uterus morphogenesis • response to retinoic acid • regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis • cell fate commitment • branching involved in ureteric bud morphogenesis • positive regulation of catalytic activity • metanephric tubule formation • regulation of protein phosphorylation • neuron differentiation • Wnt signaling pathway Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	7484	22412
Ensembl	n/a	ENSMUSG00000018486
UniProt	O14905	O35468
RefSeq (mRNA)	NM_003396 NM_001320458	NM_011719
RefSeq (protein)	NP_003387.1	NP_035849.3
Location (UCSC)	Chr 17: 46.83 – 46.89 Mb	Chr 11: 103.73 – 103.75 Mb
PubMed search	[2]	[3]
Wikidata

View/Edit Human

View/Edit Mouse

Protein Wnt-9b (formerly Wnt15^[4]) is a protein that in humans is encoded by the WNT9B gene.^[5]

References

1. "Diseases that are genetically associated with WNT9B view/edit references on wikidata".
2. "Human PubMed Reference:".
3. "Mouse PubMed Reference:".
4. 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.
5. "Entrez Gene: Wnt9b wingless-type MMTV integration site family, member 9B".