SLC2A13

Solute carrier family 2 (facilitated glucose transporter), member 13 is a protein that in humans is encoded by the SLC2A13 gene.[5]

SLC2A13
Identifiers
Aliases	SLC2A13, HMIT, solute carrier family 2 member 13
External IDs	OMIM: 611036 MGI: 2146030 HomoloGene: 43139 GeneCards: SLC2A13
Gene location (Human) Chr. Chromosome 12 (human)[1] Band 12q12 Start 39,755,025 bp[1] End 40,106,089 bp[1]
Gene location (Mouse) Chr. Chromosome 15 (mouse)[2] Band 15|15 E3 Start 91,267,696 bp[2] End 91,573,261 bp[2]
Gene ontology Molecular function • transporter activity • carbohydrate:proton symporter activity • GO:0022891 transmembrane transporter activity • glucose transmembrane transporter activity • myo-inositol:proton symporter activity Cellular component • integral component of membrane • cell membrane • membrane • integral component of plasma membrane Biological process • glucose import • transmembrane transport • myo-inositol transport • hydrogen ion transmembrane transport • hexose transport • glucose transmembrane transport Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	114134	239606
Ensembl	ENSG00000151229	ENSMUSG00000036298
UniProt	Q96QE2	Q3UHK1
RefSeq (mRNA)	NM_052885	NM_001033633
RefSeq (protein)	NP_443117	NP_001028805
Location (UCSC)	Chr 12: 39.76 – 40.11 Mb	Chr 15: 91.27 – 91.57 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. GRCh38: Ensembl release 89: ENSG00000151229 - Ensembl, May 2017
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.
5. "Entrez Gene: Solute carrier family 2 (facilitated glucose transporter), member 13". Retrieved 2011-10-23.

Further reading

• 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.