High affinity cationic amino acid transporter 1

Last updated
SLC7A1
Identifiers
Aliases SLC7A1 , ATRC1, CAT-1, ERR, HCAT1, REC1L, solute carrier family 7 member 1
External IDs OMIM: 104615 MGI: 88117 HomoloGene: 20658 GeneCards: SLC7A1
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003045

NM_001301424
NM_007513

RefSeq (protein)

NP_003036

NP_001288353
NP_031539

Location (UCSC) Chr 13: 29.51 – 29.6 Mb Chr 5: 148.26 – 148.34 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

High affinity cationic amino acid transporter 1 is a protein that in humans is encoded by the SLC7A1 gene. [5] [6]

Contents

See also

Related Research Articles

The solute carrier (SLC) group of membrane transport proteins include over 400 members organized into 66 families. Most members of the SLC group are located in the cell membrane. The SLC gene nomenclature system was originally proposed by the HUGO Gene Nomenclature Committee (HGNC) and is the basis for the official HGNC names of the genes that encode these transporters. A more general transmembrane transporter classification can be found in TCDB database.

CD98 is a glycoprotein that is a heterodimer composed of SLC3A2 and SLC7A5 that forms the large neutral amino acid transporter (LAT1). LAT1 is a heterodimeric membrane transport protein that preferentially transports branched-chain and aromatic amino acids. LAT is highly expressed in brain capillaries relative to other tissues.

<span class="mw-page-title-main">Excitatory amino acid transporter 1</span> Protein found in humans

Excitatory amino acid transporter 1 (EAAT1) is a protein that, in humans, is encoded by the SLC1A3 gene. EAAT1 is also often called the GLutamate ASpartate Transporter 1 (GLAST-1).

<span class="mw-page-title-main">Thiamine transporter 1</span> Mammalian protein found in Homo sapiens

Thiamine transporter 1, also known as thiamine carrier 1 (TC1) or solute carrier family 19 member 2 (SLC19A2) is a protein that in humans is encoded by the SLC19A2 gene. SLC19A2 is a thiamine transporter. Mutations in this gene cause thiamine-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness.

<span class="mw-page-title-main">4F2 cell-surface antigen heavy chain</span> Protein-coding gene in the species Homo sapiens

4F2 cell-surface antigen heavy chain is a protein that in humans is encoded by the SLC3A2 gene.

<span class="mw-page-title-main">SLC22A4</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 22, member 4, also known as SLC22A4, is a human gene; the encoded protein is known as the ergothioneine transporter.

<span class="mw-page-title-main">Excitatory amino acid transporter 3</span> Protein found in humans

Excitatory amino acid transporter 3 (EAAT3), is a protein that in humans is encoded by the SLC1A1 gene.

<span class="mw-page-title-main">Proton-coupled amino acid transporter 1</span> Protein-coding gene in the species Homo sapiens

Proton-coupled amino acid transporter 1 is a protein that in humans is encoded by the SLC36A1 gene.

<span class="mw-page-title-main">Y+L amino acid transporter 1</span>

Y+L amino acid transporter 1 is a protein that in humans is encoded by the SLC7A7 gene.

An amino acid transporter is a membrane transport protein that transports amino acids. They are mainly of the solute carrier family.

<span class="mw-page-title-main">Cationic amino acid transporter 3</span> Protein-coding gene in the species Homo sapiens

Cationic amino acid transporter 3 is a protein that in humans is encoded by the SLC7A3 gene.

<span class="mw-page-title-main">Monocarboxylate transporter 1</span>

Monocarboxylate transporter 1 is a ubiquitous protein that in humans is encoded by the SLC16A1 gene. It is a proton coupled monocarboxylate transporter.

<span class="mw-page-title-main">Cationic amino acid transporter 2</span> Protein-coding gene in the species Homo sapiens

Cationic amino acid transporter 2 is a protein that in humans is encoded by the SLC7A2 gene.

<span class="mw-page-title-main">Cationic amino acid transporter 4</span> Protein-coding gene in the species Homo sapiens

Cationic amino acid transporter 4 is a protein that in humans is encoded by the SLC7A4 gene.

<span class="mw-page-title-main">Sodium-dependent neutral amino acid transporter B(0)AT1</span> Protein-coding gene in the species Homo sapiens

Sodium-dependent neutral amino acid transporter B(0)AT1 is a protein that in humans is encoded by the SLC6A19 gene.

<span class="mw-page-title-main">Plasma membrane monoamine transporter</span> Protein-coding gene in the species Homo sapiens

The plasma membrane monoamine transporter (PMAT) is a low-affinity monoamine transporter protein which in humans is encoded by the SLC29A4 gene. It is known alternatively as the human equilibrative nucleoside transporter-4 (hENT4). Unlike other members of the ENT family, it is impermeable to most nucleosides, with the exception of the inhibitory neurotransmitter and ribonucleoside adenosine, which it is permeable to in a highly pH-dependent manner.

<span class="mw-page-title-main">Large neutral amino acids transporter small subunit 1</span> Protein-coding gene in the species Homo sapiens

Large neutral amino acids transporter small subunit 1, also known as 4F2 light chain, or CD98 light chain is a protein that in humans is encoded by the SLC7A5 gene.

<span class="mw-page-title-main">Y+L amino acid transporter 2</span> Protein-coding gene in the species Homo sapiens

Y+L amino acid transporter 2, also known as cationic amino acid transporter, y+ system, is a protein that in humans is encoded by the SLC7A6 gene.

<span class="mw-page-title-main">Monocarboxylate transporter 10</span>

Monocarboxylate transporter 10, also known as aromatic amino acid transporter 1 and T-type amino acid transporter 1 (TAT1) and solute carrier family 16 member 10 (SLC16A10), is a protein that in humans is encoded by the SLC16A10 gene. SLC16A10 is a member of the solute carrier family.

<span class="mw-page-title-main">Proton-coupled folate transporter</span> Mammalian protein found in Homo sapiens

The proton-coupled folate transporter is a protein that in humans is encoded by the SLC46A1 gene. The major physiological roles of PCFTs are in mediating the intestinal absorption of folate, and its delivery to the central nervous system.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000139514 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000041313 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Albritton LM, Bowcock AM, Eddy RL, Morton CC, Tseng L, Farrer LA, Cavalli-Sforza LL, Shows TB, Cunningham JM (March 1992). "The human cationic amino acid transporter (ATRC1): physical and genetic mapping to 13q12-q14". Genomics. 12 (3): 430–4. doi:10.1016/0888-7543(92)90431-Q. PMID   1348489.
  6. "Entrez Gene: SLC7A1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1".

Further reading