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]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000151229 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000036298 – 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.
^ "SLC2A13 solute carrier family 2 member 13 [ Homo sapiens (human) ]". Retrieved 2021-04-18.

Uldry M, Ibberson M, Horisberger JD, Chatton JY, Riederer BM, Thorens B (August 2001). "Identification of a mammalian H(+)-myo-inositol symporter expressed predominantly in the brain". The EMBO Journal. 20 (16): 4467–77. doi:10.1093/emboj/20.16.4467. PMC 125574. PMID 11500374.
Fu GK, Wang JT, Yang J, Au-Young J, Stuve LL (July 2004). "Circular rapid amplification of cDNA ends for high-throughput extension cloning of partial genes". Genomics. 84 (1): 205–10. doi:10.1016/j.ygeno.2004.01.011. PMID 15203218.
Bankovic J, Stojsic J, Jovanovic D, Andjelkovic T, Milinkovic V, Ruzdijic S, Tanic N (February 2010). "Identification of genes associated with non-small-cell lung cancer promotion and progression". Lung Cancer. 67 (2): 151–9. doi:10.1016/j.lungcan.2009.04.010. PMID 19473719.
Di Daniel E, Mok MH, Mead E, Mutinelli C, Zambello E, Caberlotto LL, Pell TJ, Langmead CJ, Shah AJ, Duddy G, Kew JN, Maycox PR (July 2009). "Evaluation of expression and function of the H+/myo-inositol transporter HMIT". BMC Cell Biology. 10: 54. doi:10.1186/1471-2121-10-54. PMC 2717050. PMID 19607714.
Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T (December 2009). "Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease". Nature Genetics. 41 (12): 1303–7. doi:10.1038/ng.485. PMID 19915576. S2CID 205356259.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000151229 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000036298 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "SLC2A13 solute carrier family 2 member 13 [ Homo sapiens (human) ]". Retrieved 2021-04-18.

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References

Further reading