Ataxin 10

ATXN10
Identifiers
Aliases	ATXN10, E46L, HUMEEP, SCA10, ataxin 10, ATX10
External IDs	OMIM: 611150; MGI: 1859293; HomoloGene: 40858; GeneCards: ATXN10; OMA:ATXN10 - orthologs
Gene location (Human)
Chr.	Chromosome 22 (human)
End	45,845,307 bp
RNA expression pattern
	Top expressed in
	ventricular zone; ; ganglionic eminence; ; gonad; ; prefrontal cortex; ; stromal cell of endometrium; ; islet of Langerhans; ; right ventricle; ; postcentral gyrus; ; pons; ; retinal pigment epithelium;
	n/a
	More reference expression data
	n/a
Gene ontology
Molecular function	enzyme binding; protein binding; identical protein binding;
Cellular component	cytoplasm; perinuclear region of cytoplasm; soma; plasma membrane; dendrite; membrane; extracellular space; cytosol;
Biological process	neuron projection development; nervous system development; protein homotrimerization; cilium assembly;
	Sources:Amigo / QuickGO
Orthologs
	25814
	54138
	ENSG00000130638
	ENSMUSG00000016541
	Q9UBB4
	P28658
	NM_013236; NM_001167621
	NM_016843
	NP_001161093; NP_037368
	NP_058539
	Wikidata
View/Edit Human	View/Edit Mouse

Ataxin-10 is a protein that in humans is encoded by the ATXN10 gene.^[4]^[5]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000130638 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Zu L, Figueroa KP, Grewal R, Pulst SM (Apr 1999). "Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22". Am J Hum Genet. 64 (2): 594–9. doi:10.1086/302247. PMC 1377770. PMID 9973298.
^ "Entrez Gene: ATXN10 ataxin 10".