solute carrier family 19 member 2

Summary
Gene Symbol
  • SLC19A2
Organism
Homo sapiens (human)
NCBI Gene
10560
PubChem
10560
Alliance of Genome Resources
Annotation
Keyword
  • Acetylation
  • Alternative splicing
  • Cell membrane
  • Deafness
  • Diabetes mellitus
  • Disease variant
  • Glycoprotein
  • Phosphoprotein
  • Reference proteome
  • Transmembrane helix
  • Transport
Proteins
Displaying all 3 entries
UniProt Protein Name
O60779
  • Solute carrier family 19 member 2
  • Thiamine carrier 1
A0A024R928
A0A024R8Y5
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
transporter
Functional Category
  • O: Posttranslational modification, protein turnover, chaperones
  • P: Inorganic ion transport and metabolism
  • T: Signal transduction mechanisms
Displaying all 2 entries
Gene Ontology
vitamin transmembrane transport
vitamin transport
Displaying all 2 entries
InterPro
MFS transporter superfamily
Reduced folate carrier
Disease
Disease Ontology
Displaying all 4 entries
DO ID Disease Name Source
DOID:0090117 thiamine-responsive megaloblastic anemia syndrome
DOID:13382 megaloblastic anemia
DOID:784 chronic kidney disease
DOID:9351 diabetes mellitus

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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