SLC2A13

SLC2A13
Identifiers
Aliases	SLC2A13, HMIT, solute carrier family 2 member 13
External IDs	OMIM: 611036; MGI: 2146030; HomoloGene: 43139; GeneCards: SLC2A13; OMA:SLC2A13 - orthologs
Gene location (Human)
Chr.	Chromosome 12 (human)
End	40,106,089 bp
Gene location (Mouse)
Chr.	Chromosome 15 (mouse)
End	91,457,464 bp
RNA expression pattern
	Top expressed in
	lateral nuclear group of thalamus; ; pars reticulata; ; endothelial cell; ; pars compacta; ; Brodmann area 23; ; Brodmann area 46; ; external globus pallidus; ; superior frontal gyrus; ; entorhinal cortex; ; middle temporal gyrus;
	Top expressed in
	olfactory tubercle; ; suprachiasmatic nucleus; ; habenula; ; dorsal striatum; ; nucleus accumbens; ; subiculum; ; substantia nigra; ; medial dorsal nucleus; ; lateral septal nucleus; ; paraventricular nucleus of hypothalamus;
	More reference expression data
	n/a
Gene ontology
Molecular function	transporter activity; carbohydrate:proton symporter activity; transmembrane transporter activity; glucose transmembrane transporter activity; myo-inositol:proton symporter activity;
Cellular component	integral component of membrane; plasma membrane; membrane; integral component of plasma membrane;
Biological process	glucose import; transmembrane transport; myo-inositol transport; proton transmembrane transport; hexose transmembrane transport; glucose transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
	114134
	239606
	ENSG00000151229
	ENSMUSG00000036298
	Q96QE2
	Q3UHK1
	NM_052885
	NM_001033633
	NP_443117
	NP_001028805
	Wikidata
View/Edit Human	View/Edit Mouse

Proton myo-inositol cotransporter, also known as solute carrier family 2 member 13 is a protein that in humans is encoded by the SLC2A13 gene.^[5]