SLC2A13

Protein-coding gene in the species Homo sapiens
SLC2A13
Identifiers
AliasesSLC2A13, HMIT, solute carrier family 2 member 13
External IDsOMIM: 611036 MGI: 2146030 HomoloGene: 43139 GeneCards: SLC2A13
Gene location (Human)
Chromosome 12 (human)
Chr.Chromosome 12 (human)[1]
Chromosome 12 (human)
Genomic location for SLC2A13
Genomic location for SLC2A13
Band12q12Start39,755,025 bp[1]
End40,106,089 bp[1]
Gene location (Mouse)
Chromosome 15 (mouse)
Chr.Chromosome 15 (mouse)[2]
Chromosome 15 (mouse)
Genomic location for SLC2A13
Genomic location for SLC2A13
Band15|15 E3Start91,151,899 bp[2]
End91,457,464 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • endothelial cell

  • Brodmann area 23

  • Brodmann area 46

  • external globus pallidus

  • superior frontal gyrus

  • entorhinal cortex

  • middle temporal gyrus

  • postcentral gyrus

  • pancreatic epithelial cell

  • right ventricle
Top expressed in
  • olfactory tubercle

  • suprachiasmatic nucleus

  • habenula

  • nucleus accumbens

  • subiculum

  • substantia nigra

  • medial dorsal nucleus

  • paraventricular nucleus of hypothalamus

  • primary motor cortex

  • dorsomedial hypothalamic nucleus
More reference expression data
BioGPS
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
SpeciesHumanMouse
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 MbChr 15: 91.15 – 91.46 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/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

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

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.
  • v
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By group
SLC1–10
(1):
(2):
(3):
(4):
(5):
(6):
(7):
(8):
  • Na+/Ca2+ exchanger
(9):
(10):
SLC11–20
(11):
(12):
(13):
(14):
(15):
(16):
(17):
(18):
(19):
(20):
SLC21–30
(21):
(22):
(23):
  • Na+-dependent ascorbic acid transporter
(24):
  • Na+/(Ca2+-K+) exchanger
(25):
(26):
(27):
(28):
(29):
(30):
SLC31–40
(31):
(32):
(33):
(34):
(35):
(36):
(37):
(38):
(39):
(40):
  • basolateral iron transporter
SLC41–48
(41):
(42):
(43):
  • Na+-independent, system-L like amino-acid transporter
(44):
(45):
(46):
(47):
(48):
SLCO1–4
Symporter, Cotransporter
  • Na+/K+,Cl
  • Na+/Pi3
  • Na+/Cl
  • Na+/glucose
  • Na+/I
  • Cl/K+
Antiporter (exchanger)
  • Na+/H+
  • Na+/Ca2+
    • Na+/(Ca2+-K+) - Cl/HCO
      3
      (Band 3)
  • Cl-formate
  • Cl-oxalate
see also solute carrier disorders


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