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Protein Coding Gene : Slc52a2 solute carrier protein 52, member 2

Primary Identifier  MGI:1289288 Organism  mouse, laboratory
Chromosome  15 NCBI Gene Number  52710
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables riboflavin transmembrane transporter activity. Involved in flavin adenine dinucleotide biosynthetic process and riboflavin metabolic process. Is active in plasma membrane. Human ortholog(s) of this gene implicated in Brown-Vialetto-Van Laere syndrome 2 and riboflavin deficiency. Orthologous to several human genes including SLC52A2 (solute carrier family 52 member 2).
PHENOTYPE: Mice homozygous for a null allele die prior to E10.5. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 2010003P03 gene,
  • GPCR42,
  • MGI:1923771,
  • 2010003P03Rik,
  • DNA segment, Chr 15, ERATO Doi 747, expressed,
  • G protein-coupled receptor 172B,
  • Gpr172b,
  • PAR2,
  • Rfvt2,
  • Slc52a2,
  • solute carrier protein 52, member 2,
  • D15Ertd747e

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

5 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

4 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For