solute carrier family 25 member 19

Summary
Gene Symbol
  • SLC25A19
Organism
Homo sapiens (human)
NCBI Gene
60386
PubChem
60386
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Antiport
  • Disease variant
  • Mitochondrion
  • Neuropathy
  • Phosphoprotein
  • Reference proteome
  • Repeat
  • Transmembrane
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
Q5JPC1
  • Solute carrier family 25 member 19
Q9HC21
  • Mitochondrial thiamine pyrophosphate transporter
  • Mitochondrial uncoupling protein 1
  • Solute carrier family 25 member 19
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Mitochondrial carrier
Functional Category
  • G: Carbohydrate transport and metabolism
  • K: Transcription
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:10907 microcephaly
DOID:655 inherited metabolic disorder

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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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