solute carrier family 38 member 3

Summary
Gene Symbol
  • SLC38A3
Organism
Homo sapiens (human)
NCBI Gene
10991
PubChem
10991
Alliance of Genome Resources
Annotation
Keyword
  • Amino-acid transport
  • Antiport
  • Cell membrane
  • Disease variant
  • Disulfide bond
  • Epilepsy
  • Glycoprotein
  • Intellectual disability
  • Reference proteome
  • Sodium transport
  • Symport
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q99624
  • N-system amino acid transporter 1
  • Na(+)-coupled neutral amino acid transporter 3
  • Solute carrier family 38 member 3
  • System N amino acid transporter 1
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Amino acid transporter
Functional Category
  • E: Amino acid transport and metabolism
  • M: Cell wall/membrane/envelope biogenesis
  • T: Signal transduction mechanisms
Displaying 1 entry
InterPro
Amino acid transporter, transmembrane domain
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:0050758 metabolic acidosis
DOID:0070388 developmental and epileptic encephalopathy 102
DOID:11832 visual epilepsy

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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: December 9, 2024