PARD3B

PARD3B
Identifiers
Aliases	PARD3B, ALS2CR19, PAR3B, PAR3L, PAR3LC, PAR3beta, Par3Lb, par-3 family cell polarity regulator beta
External IDs	MGI: 1919301; HomoloGene: 35389; GeneCards: PARD3B; OMA:PARD3B - orthologs
Gene location (Human)
Chr.	Chromosome 2 (human)
End	205,620,162 bp
Gene location (Mouse)
Chr.	Chromosome 1 (mouse)
End	62,681,443 bp
RNA expression pattern
	Top expressed in
	sural nerve; ; ventricular zone; ; Achilles tendon; ; epithelium of colon; ; saphenous vein; ; tibial arteries; ; mucosa of ileum; ; testicle; ; gonad; ; skin of hip;
	Top expressed in
	Rostral migratory stream; ; crypt of lieberkuhn of small intestine; ; internal carotid artery; ; external carotid artery; ; sciatic nerve; ; lumbar spinal ganglion; ; renal corpuscle; ; ciliary body; ; iris; ; intestinal villus;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding; phosphatidylinositol binding;
Cellular component	membrane; endomembrane system; bicellular tight junction; cell junction; nucleoplasm; nuclear body; protein-containing complex; cytoplasm; adherens junction; cell cortex; apical plasma membrane; apical junction complex;
Biological process	cell division; cell cycle; microtubule cytoskeleton organization; cell adhesion; protein localization; establishment of cell polarity; establishment or maintenance of epithelial cell apical/basal polarity; establishment of centrosome localization;
	Sources:Amigo / QuickGO
Orthologs
	117583
	72823
	ENSG00000116117
	ENSMUSG00000052062
	Q8TEW8
	Q9CSB4
	NM_001302769; NM_057177; NM_152526; NM_205863
	NM_001081050
	NP_001289698; NP_476518; NP_689739; NP_995585
	NP_001074519
	Wikidata
View/Edit Human	View/Edit Mouse

Partitioning defective 3 homolog B is a protein that in humans is encoded by the PARD3B gene.