solute carrier family 25 member 1

Summary
Gene Symbol
  • SLC25A1
Organism
Homo sapiens (human)
External Links
NCBI Gene
6576
PubChem
6576
Alliance of Genome Resources
Annotation
Keyword
  • Antiport
  • Congenital myasthenic syndrome
  • Disease variant
  • Mitochondrion inner membrane
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Transmembrane
  • Transmembrane helix
Proteins
Displaying all 3 entries
UniProt Protein Name
D3DX16
D9HTE9
P53007
  • Citrate transport protein
  • Mitochondrial citrate carrier
  • Solute carrier family 25 member 1
  • Tricarboxylate carrier protein
Gene Ontology (GO)
GO Hierarchy
Disease
Disease Ontology
Displaying all 6 entries
DO ID Disease Name Source
DOID:0050573 2-hydroxyglutaric aciduria
DOID:0060413 chromosome 22q11.2 deletion syndrome, distal
DOID:0111619 combined D-2- and L-2-hydroxyglutaric aciduria
DOID:11198 DiGeorge syndrome
DOID:3635 congenital myasthenic syndrome
DOID:700 mitochondrial metabolism disease

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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: August 19, 2024