Slc52a2 - solute carrier protein 52, member 2 Gene
Also Known as PAR2; RFT1; Rfvt2; mRFT1; GPCR42; Gpr172b; D15Ertd747e; 2010003P03Rik
Species: Mus musculus
Summary
Predicted to enable 4-hydroxybutyrate receptor activity and riboflavin transmembrane transporter activity. Predicted to be involved in riboflavin transport. Predicted to be located in plasma membrane. Predicted to be integral component of 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). [provided by Alliance of Genome Resources, Apr 2022]
Slc52a2 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_029643.4 | NP_083919.1 | solute carrier family 52, riboflavin transporter, member 2 precursor |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables riboflavin transmembrane transporter activity |
IDA
IDA: Inferred from direct assay
|
26791833 | MGI |
| enables riboflavin transmembrane transporter activity |
IMP
IMP: Inferred from mutant phenotype
|
23911957 | MGI |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in flavin adenine dinucleotide biosynthetic process |
IDA
IDA: Inferred from direct assay
|
26791833 | MGI |
| involved in flavin adenine dinucleotide biosynthetic process |
IMP
IMP: Inferred from mutant phenotype
|
23911957 | MGI |
| involved in riboflavin metabolic process |
IDA
IDA: Inferred from direct assay
|
26791833 | MGI |
| involved in riboflavin metabolic process |
IMP
IMP: Inferred from mutant phenotype
|
23911957 | MGI |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| is active in plasma membrane |
IDA
IDA: Inferred from direct assay
|
26791833 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
solute carrier family 52, riboflavin transporter, member 2 |
|
|