solute carrier family 25 member 10

Summary
Gene Symbol
  • SLC25A10
Organism
Homo sapiens (human)
NCBI Gene
1468
PubChem
1468
Alliance of Genome Resources
JoGo
SLC25A10
TogoVar
SLC25A10
Annotation
Keyword
  • Alternative splicing
  • Antiport
  • Disease variant
  • Lipid transport
  • Mitochondrion inner membrane
  • Primary mitochondrial disease
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Transmembrane helix
  • Transport
Proteins
Displaying all 5 entries
UniProt Protein Name
Q9UBX3
  • Solute carrier family 25 member 10
A0A0S2Z382
  • Solute carrier family 25 member 10
F6RGN5
A0A0S2Z3G3
  • Solute carrier family 25 member 10
B4E1E9
  • Solute carrier family 25 member 10
Gene Ontology (GO)
Displaying entries 1 - 5 of 15 in total
GO Term Evidence Code PMID
gluconeogenesis
monoatomic ion transport
ion transport
dicarboxylic acid transport
lipid transport
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Mitochondrial uncoupling protein
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0070450 mitochondrial DNA depletion syndrome 19

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026