Slc46a1 - solute carrier family 46 member 1 Gene

Also Known as rPCFT; RGD1309472

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 303333

Summary

Enables folic acid transmembrane transporter activity. Involved in folic acid transport. Located in brush border membrane. Biomarker of chronic kidney disease. Human ortholog(s) of this gene implicated in hereditary folate malabsorption. Orthologous to human SLC46A1 (solute carrier family 46 member 1). [provided by Alliance of Genome Resources, Apr 2022]

Slc46a1 Products (1)

mRNA Protein Name
NM_001013969.1 NP_001013991.1 proton-coupled folate transporter

Gene Ontology

  • Cellular Component
Cellular Component GO Annotation Evidence References Source
located in brush border membrane IDA
IDA: Inferred from direct assay
23287122 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

proton-coupled folate transporter

  • PCFT/HCP1

  • heme carrier protein 1

  • solute carrier family 46 (folate transporter), member 1

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13260 SLC46A1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc46a1 NCBI NCBI:113235