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SLC3A1 wt Allele

Known as: RBAT, Solute Carrier Family 3 (Cystine, Dibasic and Neutral Amino Acid Transporters), Member 1 Gene, NBAT 
Human SLC3A1 wild-type allele is located in the vicinity of 2p16.3 and is approximately 46 kb in length. This allele, which encodes neutral and basic… 
National Institutes of Health

Related topics

Related topics

8 relations
2p16.3Carbohydrate MetabolismCystinuriaHomo sapiens

Narrower (1)

Neutral and Basic Amino Acid Transport Protein rBAT

Broader (1)

SLC3A1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Rapid Communication: Variance component estimates for Charolais-sired fed cattle and relative economic impact of bovine respiratory disease.
Variance components were estimated and relative economic importance of bovine respiratory disease (BRD) was derived from 3 yr of… 
2015
2015
Planar dicyclic B6S6, B6S6(-), and B6S6(2-) clusters: boron sulfide analogues of naphthalene.
Inorganic analogues of hydrocarbons or polycyclic aromatic hydrocarbons (PAHs) are of current interest in chemistry. Based upon… 
2009
2009
Gene polymorphisms of renin angiotensin system and serotonin transporter gene in patients with vasovagal syncope.
UNLABELLED Objective of this study was to compare the distribution frequencies of gene polymorphisms of renin-angiotensin and… 
2007
2007
Renin-angiotensin system polymorphisms and renal graft function in renal transplant recipients.
OBJECTIVE To analyze the role of 3 polymorphisms of the renin-angiotensin system (RAS) in renal transplant recipients (RTRs) and… 
2002
2002
Cystine Transport Activity of Heterozygous rBAT Mutants Expressed in Xenopus Oocytes
The rBAT gene encodes a transport protein for cystine and dibasic amino acids. It is a candidate gene for type I cystinuria, a… 
2001
2001
Uteroplacental Insufficiency Alters Liver and Skeletal Muscle Branched-Chain Amino Acid Metabolism in Intrauterine Growth-Restricted Fetal Rats
Uteroplacental insufficiency causes intrauterine growth restriction (IUGR) and decreases plasma levels of the branched-chain… 
Review
2000
Review
2000
The Molecular Basis of Cystinuria: An Update
Cystinuria is a hereditary disorder of cystine and dibasic amino acid transport across the luminal membrane of renal proximal… 
1996
1996
rBAT is an Amino Acid Exchanger with Variable Stoichiometry
Abstract. The rBAT protein, when expressed in Xenopus oocytes, was previously shown to reproduce the selectivity of the Na… 
1996
1996
Genomic structure and organization of the human rBAT gene (SLC3A1).
Cystinuria is an autosomal recessive disorder of amino acid transport, manifesting as three phenotypes (I, II, and III). An amino… 
1989
1989
Glottic and cervical tracheal narrowing in patients with obstructive sleep apnea.
There are several studies showing that patients with idiopathic obstructive sleep apnea (OSA) have a narrow and collapsible… 
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