Slc52a2 - solute carrier family 52 member 2 Gene
Also Known as rRFT1; Gpr172a; Gpr172b; RGD1560410
Species: Rattus norvegicus
Summary
Enables riboflavin transmembrane transporter activity. Involved in riboflavin transport. Is 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_001109670.1 | NP_001103140.1 | solute carrier family 52, riboflavin transporter, member 2 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables riboflavin transmembrane transporter activity |
IDA
IDA: Inferred from direct assay
|
18632736 | RGD |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in riboflavin transport |
IDA
IDA: Inferred from direct assay
|
18632736 | RGD |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in plasma membrane |
IDA
IDA: Inferred from direct assay
|
18632736 | RGD |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
solute carrier family 52, riboflavin transporter, member 2 |
|
|