Gene

slc19a2

ID
ZDB-GENE-110411-262
Name
solute carrier family 19 member 2
Symbol
slc19a2 Nomenclature History
Previous Names
  • si:ch211-194e2.2
Type
protein_coding_gene
Location
Chr: 6 Mapping Details/Browsers
Description
Predicted to have thiamine transmembrane transporter activity. Predicted to be involved in thiamine transport and transmembrane transport. Predicted to localize to plasma membrane. Human ortholog(s) of this gene implicated in diabetes mellitus; megaloblastic anemia; and thiamine-responsive megaloblastic anemia syndrome. Orthologous to human SLC19A2 (solute carrier family 19 member 2).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With slc19a2 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
thiamine-responsive megaloblastic anemia syndrome Alliance Thiamine-responsive megaloblastic anemia syndrome 249270
Associated With slc19a2 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR002666 Reduced folate carrier
Homologous_superfamily IPR036259 MFS transporter superfamily
Domain Details Per Protein
Protein Length MFS transporter superfamily Reduced folate carrier
UniProtKB:E7F340 463
UniProtKB:A0A2R8QIQ8 274
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations