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SLC7A7 gene

Known as: y+LAT-1, y(+)LAT1, SOLUTE CARRIER FAMILY 7 (CATIONIC AMINO ACID TRANSPORTER, y+ SYSTEM), MEMBER 7 
This gene plays a role in the transport of cationic amino acids.
National Institutes of Health

Related topics

Related topics

6 relations
Homo sapiensIonophore activityLigand BindingMolecular Transport

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Lysinuric protein intolerance with homozygous SLC7A7 mutation caused by maternal uniparental isodisomy of chromosome 14
Lysinuric protein intolerance (LPI) is caused by mutations in the SLC7A7 gene at 14q11.2. Its clinical presentation includes… 
2017
2017
Association of three common single nucleotide polymorphisms of SLC7A7 with the development of glioma in a Chinese population.
Gliomas are brain tumors that can be seriously damaging to human health. The SLC7 family is involved in amino acid or peptide… 
2017
2017
Association of six SNPs in SLC 7 A 7 with glioma risk in a Chinese population
Glioma is the most common type of tumors in the central nervous system. We performed a case-control study in a Chinese population… 
2016
2016
CDX2 increases SLC7A7 expression and proliferation of pig intestinal epithelial cells
Nutrient absorption mediated by nutrient transporters expressed in the intestinal epithelium supplies substrates to support… 
2013
2013
Molecular and clinical evaluation of Turkish patients with lysinuric protein intolerance.
2012
2012
Exploring the transcriptomic variation caused by the Finnish founder mutation of lysinuric protein intolerance (LPI).
2012
2012
The First Korean Case of Lysinuric Protein Intolerance: Presented with Short Stature and Increased Somnolence
Lysinuric protein intolerance (LPI) is a rare inherited metabolic disease, caused by defective transport of dibasic amino acids… 
2007
2007
Renal Fanconi syndrome with ultrastructural defects in lysinuric protein intolerance
SummaryRenal Fanconi syndrome developed rapidly in a 3-year-old Moroccan girl with established lysinuric protein intolerance. She… 
2005
2005
Multiple pathways for cationic amino acid transport in rat thyroid epithelial cell line PC Cl3.
Information regarding cationic amino acid transport systems in thyroid is limited to Northern blot detection of y(+)LAT1 mRNA in… 
2005
2005
A y+LAT-1 mutant protein interferes with y+LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance
Lysinuric protein intolerance (LPI) is an inherited aminoaciduria caused by defective cationic amino acid (CAA) transport at the… 
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