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Browse our SLC46A1 Proteins (SLC46A1)

Full name:
Solute Carrier Family 46 (Folate Transporter), Member 1 Proteins (SLC46A1)
On are 3 Solute Carrier Family 46 (Folate Transporter), Member 1 (SLC46A1) Proteins from 2 different suppliers available. Additionally we are shipping SLC46A1 Antibodies (25) and many more products for this protein. A total of 32 SLC46A1 products are currently listed.
1110002C08Rik, D11Ertd18e, G21, HCP1, Pcft, RGD1309472, TRPE
list all proteins Gene Name GeneID UniProt
SLC46A1 113235 Q96NT5
Rat SLC46A1 SLC46A1 303333 Q5EBA8
SLC46A1 52466 Q6PEM8

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SLC46A1 Proteins (SLC46A1) by Origin

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Human Solute Carrier Family 46 (Folate Transporter), Member 1 (SLC46A1) interaction partners

  1. we observed nominally significant (but not definitive) associations between SLC46A1 SNPs and NTDs and oral clefts, and this finding warrants follow-up in other populations.

  2. A homology model of PCFT, based upon the Escherichia coliglycerol 3-phosphate transporter structure, predicted that PCFT transmembrane domains (TMDs) 1, 2, 7, and 11 form an extracellular gate in the inward-open conformation.

  3. We conclude that SLC46A1/PCFT and SLC19A1/RFC-1 (show SLC19A1 Proteins) are associated with DFS (show FST Proteins) of patients with colorectal cancer and hypothesize that poor response to 5-fluorouracil plus leucovorin therapy in some patients may be linked to low expression of these genes.

  4. Report sustained inhibition of PCFT by myricetin.

  5. this is the first study to simultaneously evaluate both DNA methylation (show HELLS Proteins) and protein expression of all three folate transporter genes, FOLR1 (show FOLR1 Proteins), PCFT, and RFC1 (show RFC1 Proteins), in colorectal cancer.

  6. the RFC1 (show RFC1 Proteins) G80A polymorphism does not seem to be a good marker of MTX (show MTX1 Proteins)-related toxicity in pediatric ALL.

  7. The current study addresses the role of Tyr (show TYR Proteins) residues in SLC46A1 function; and identifies four residues that enhance the affinity of the carrier for its substrates and decrease the rate at which the carrier oscillates between its conformational states.

  8. SLC46A1 genotype may help to identify patients with increased risk of methotrexate-related toxicity.

  9. Data indicate that 28/33 cysteine-less proton-coupled folate transporter (PCFT) mutant HeLa cells were active for [(3)H]methotrexate uptake.

  10. The molecular bases for methotrexate resistance associated with loss of SLC19A1 (show SLC19A1 Proteins) transport and for hereditary folate malabsorption, attributable to mutant SLC46A1, were determned (review).

Mouse (Murine) Solute Carrier Family 46 (Folate Transporter), Member 1 (SLC46A1) interaction partners

  1. Functional regulation of P-glycoprotein at the blood-brain barrier in proton-coupled folate transporter (PCFT) mutant mice.

  2. Hemochromatosis (show HFE Proteins) is associated not only with excessive accumulation of free iron in the retina and retinal pigment epithelium but also with excessive accumulation of heme.

  3. In vivo folate uptake experiments demonstrated a systemic folate deficiency caused by disruption of PCFT-mediated intestinal folate uptake, thus confirming in vivo a critical role of the PCFT protein in intestinal folate transport and erythropoiesis.

  4. heme carrier protein 1(HCP 1)is the long-sought intestinal heme transporter and was iron regulated and localized to the brush-border membrane of duodenal enterocytes in iron deficiency. Its mRNA was expressed in duodenum and regulated by hypoxia

  5. Slc46a1/PCFT plays critical role in intestinal folate absorption.

  6. Intestinal folate uptake process undergoes differentiation-dependent regulation and that this regulation is mediated via changes in the level of expression of both the RFC (show SLC19A1 Proteins) and PCFT.

SLC46A1 Protein Profile

Protein Summary

This gene encodes a transmembrane proton-coupled folate transporter protein that facilitates the movement of folate and antifolate substrates across cell membranes, optimally in acidic pH environments. This protein is also expressed in the brain and choroid plexus where it transports folates into the central nervous system. This protein further functions as a heme transporter in duodenal enterocytes, and potentially in other tissues like liver and kidney. Its localization to the apical membrane or cytoplasm of intestinal cells is modulated by dietary iron levels. Mutations in this gene are associated with autosomal recessive hereditary folate malabsorption (HFM) disease. HFM is characterized by folate deficiency due to reduced intestinal folate absorption and subsequent anemia, hypoimmunoglobulinemia, and recurrent infections. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

Alternative names and synonyms associated with SLC46A1

  • solute carrier family 46 (folate transporter), member 1 (SLC46A1)
  • solute carrier family 46 (folate transporter), member 1 (slc46a1)
  • solute carrier family 46 (folate transporter), member 1 (Slc46a1)
  • solute carrier family 46, member 1 (Slc46a1)
  • 1110002C08Rik protein
  • D11Ertd18e protein
  • G21 protein
  • HCP1 protein
  • Pcft protein
  • RGD1309472 protein
  • TRPE protein

Protein level used designations for SLC46A1

solute carrier family 46, member 1 , solute carrier family 46 (folate transporter), member 1 , proton-coupled folate transporter-like , heme carrier protein 1 , proton-coupled folate transporter , PCFT/HCP1 , retinal pigment epithelilum transporter , retinal pigment epithelium transporter , solute carrier family 46 member 1

491166 Canis lupus familiaris
708727 Macaca mulatta
100072047 Equus caballus
100145771 Xenopus (Silurana) tropicalis
100411886 Callithrix jacchus
100468045 Ailuropoda melanoleuca
100599656 Nomascus leucogenys
113235 Homo sapiens
303333 Rattus norvegicus
511097 Bos taurus
52466 Mus musculus
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