FAQ

SLC52A1 gene

Known as: PERV-A RECEPTOR 2, G PROTEIN-COUPLED RECEPTOR 42, solute carrier family 52 member 1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2008-2018
02420082018

Related topics

Related topics

2 relations
GPR39 geneGPR42 gene

Related mentions per year

Related mentions per year

1997-2018
1990200020102020
SLC52A1 gene
GPR39 gene
GPR42 gene

Papers overview

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2017
2017
Three cysteine residues of SLC52A1, a receptor for the porcine endogenous retrovirus-A (PERV-A), play a critical role in cell surface expression and infectivity.
Porcine endogenous retrovirus-A (PERV-A), a gammaretrovirus, infects human cells in vitro, thus raising the potential risk of… (More)
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2016
2016
Comparison of rice flowering-time genes under paddy conditions
Heading date is one of most important agronomic traits in rice. Flowering regulatory mechanisms have been elucidated in many… (More)
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2014
2014
Identification and characterization of 5'-flanking region of the human riboflavin transporter 1 gene (SLC52A1).
The human SLC52A1 gene encodes the riboflavin transporter-1 (RFVT-1), a plasma membrane protein that transports vitamin B2… (More)
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2013
2013
Natural Variation of the RICE FLOWERING LOCUS T 1 Contributes to Flowering Time Divergence in Rice
In rice (Oryza sativa L.), there is a diversity in flowering time that is strictly genetically regulated. Some indica cultivars… (More)
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2012
2012
Ectopic expression of OsMADS45 activates the upstream genes Hd3a and RFT1 at an early development stage causing early flowering in rice
The rice gene, OsMADS45, which belongs to the MADS-box E class gene, participates in the regulation of floral development… (More)
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2011
2011
Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B.
Riboflavin, or vitamin B2, is a precursor to flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) molecules… (More)
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2010
2010
Identification and comparative functional characterization of a new human riboflavin transporter hRFT3 expressed in the brain.
We isolated cDNA coding a new human riboflavin transporter (hRFT)3, which exhibits 86.7 and 44.1% amino acid identity with hRFT1… (More)
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2009
2009
Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In)
Very recently, Haeuptle and colleagues described a new glycosylation defect due to RFT1 deficiency (CDG In). Accumulation of… (More)
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Highly Cited
2008
Highly Cited
2008
Hd3a and RFT1 are essential for flowering in rice.
RICE FLOWERING LOCUS T 1 (RFT1/FT-L3) is the closest homologue of Heading date 3a (Hd3a), which is thought to encode a mobile… (More)
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2008
2008
Identification and functional characterization of a novel human and rat riboflavin transporter, RFT1.
Absorption of riboflavin is mediated by transporter(s). However, a mammalian riboflavin transporter has yet to be identified. In… (More)
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