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SLC25A16

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Protein-coding gene in the species Homo sapiens
SLC25A16
Identifiers
AliasesSLC25A16, D10S105E, GDA, GDC, HGT.1, ML7, hML7, solute carrier family 25 member 16
External IDsOMIM: 139080; MGI: 1920382; HomoloGene: 21858; GeneCards: SLC25A16; OMA:SLC25A16 - orthologs
Gene location (Human)
Chromosome 10 (human)
Chr.Chromosome 10 (human)
Chromosome 10 (human)Genomic location for SLC25A16Genomic location for SLC25A16
Band10q21.3Start68,477,998 bp
End68,527,523 bp
Gene location (Mouse)
Chromosome 10 (mouse)
Chr.Chromosome 10 (mouse)
Chromosome 10 (mouse)Genomic location for SLC25A16Genomic location for SLC25A16
Band10|10 B4Start62,756,412 bp
End62,782,277 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • jejunal mucosa

  • right lobe of liver

  • adipose tissue

  • gonad

  • mammary gland

  • lactiferous gland

  • epithelium of colon

  • lactiferous duct

  • corpus epididymis

  • duodenum
Top expressed in
  • left lobe of liver

  • human kidney

  • right kidney

  • Epithelium of choroid plexus

  • parotid gland

  • retinal pigment epithelium

  • lacrimal gland

  • otolith organ

  • utricle

  • seminal vesicula
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

8034

73132

Ensembl

ENSG00000122912

ENSMUSG00000071253

UniProt

P16260

Q8C0K5

RefSeq (mRNA)
NM_152707
NM_001324312
NM_001324313
NM_001324314
NM_001324315

NM_001324317

NM_175194

RefSeq (protein)
NP_001311241
NP_001311242
NP_001311243
NP_001311244
NP_001311246

NP_689920

NP_780403

Location (UCSC)Chr 10: 68.48 – 68.53 MbChr 10: 62.76 – 62.78 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16 is a protein in humans that is encoded by the SLC25A16 gene.

This gene encodes a protein that contains three tandemly repeated mitochondrial carrier protein domains. The encoded protein is localized in the inner membrane and facilitates the rapid transport and exchange of molecules between the cytosol and the mitochondrial matrix space. This gene has a possible role in Graves' disease. .

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000122912 – Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000071253 – 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 25 (mitochondrial carrier; Graves disease autoantigen), member 16". Retrieved 2012-11-27.

Further reading


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