KIAA0196

WASHC5
Identifiers
Aliases	WASHC5, RTSC, SPG8, RTSC1, KIAA0196, WASH complex subunit 5
External IDs	OMIM: 610657; MGI: 2146110; HomoloGene: 8898; GeneCards: WASHC5; OMA:WASHC5 - orthologs
Gene location (Human)
Chr.	Chromosome 8 (human)
End	125,091,819 bp
Gene location (Mouse)
Chr.	Chromosome 15 (mouse)
End	59,246,016 bp
RNA expression pattern
	Top expressed in
	corpus callosum; ; Achilles tendon; ; stromal cell of endometrium; ; monocyte; ; bone marrow cell; ; epithelium of nasopharynx; ; epithelium of colon; ; islet of Langerhans; ; C1 segment; ; spinal ganglia;
	Top expressed in
	endothelial cell of lymphatic vessel; ; hand; ; stroma of bone marrow; ; calvaria; ; epithelium of lens; ; foot; ; vas deferens; ; condyle; ; iris; ; otolith organ;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding;
Cellular component	cytoplasm; cytosol; endosome; early endosome; WASH complex; endoplasmic reticulum; nucleoplasm; neuron projection; soma;
Biological process	protein transport; endosomal transport; oocyte maturation; polar body extrusion after meiotic divisions; meiotic spindle assembly; positive regulation of neuron projection development;
	Sources:Amigo / QuickGO
Orthologs
	9897
	223593
	ENSG00000164961
	ENSMUSG00000022350
	Q12768
	Q8C2E7
	NM_014846; NM_001330609
	NM_153548
	NP_001317538; NP_055661
	NP_705776
	Wikidata
View/Edit Human	View/Edit Mouse

KIAA0196 (also known as strumpellin) is a human gene.^[5] The product is a protein that is a component of the WASH complex, which regulates actin assembly on intracellular vesicles.^[6] Mutations in KIAA0196 are implicated in some forms of hereditary spastic paraplegia.^[7]