Gene

slc52a3-2b

ID
ZDB-GENE-040704-21
Name
solute carrier family 52 member 3-2b
Symbol
slc52a3-2b Nomenclature History
Previous Names
  • slc52a3b (1)
  • zgc:91890 (1)
Type
protein_coding_gene
Location
Chr: 16 Mapping Details/Browsers
Description
Predicted to have riboflavin transmembrane transporter activity. Predicted to be involved in riboflavin transport. Predicted to localize to integral component of plasma membrane. Human ortholog(s) of this gene implicated in Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. Is expressed in several structures, including alar plate midbrain region; epidermis; immature eye; midbrain; and pectoral fin. Orthologous to human SLC52A3 (solute carrier family 52 member 3).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
7 figures from Thisse et al., 2004
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 slc52a3-2b Human Ortholog
No data available
Associated With slc52a3-2b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR009357 Solute carrier family 52, riboflavin transporter
Domain Details Per Protein
Protein Length Solute carrier family 52, riboflavin transporter
UniProtKB:Q6GMG6 452
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