solute carrier family 52 member 3

Summary
Gene Symbol
  • SLC52A3
Organism
Homo sapiens (human)
NCBI Gene
113278
PubChem
113278
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cell membrane
  • Cytoplasm
  • Deafness
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Nucleus
  • Phosphoprotein
  • Reference proteome
  • Transmembrane helix
  • Transport
Proteins
Displaying 1 entry
UniProt Protein Name
Q9NQ40
  • Riboflavin transporter 2
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Solute carrier family 52 riboflavin transporter
Functional Category
  • E: Amino acid transport and metabolism
  • M: Cell wall/membrane/envelope biogenesis
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0080632 Fazio-Londe disease
DOID:0080785 Brown-Vialetto-Van Laere syndrome 1

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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 7, 2025