SLC7A5
Sign in to saveAlso known as 4F2LC, CD98, D16S469E, E16, LAT1, MPE16, hLAT1, solute carrier family 7 member 5
protein-coding gene in the species Homo sapiens
In the Vinony graph
Vinony's link graph records 261 inbound references to SLC7A5, and connects out to PubMed, human chromosome 16 and Ensembl genome database project.
It is catalogued under topics including Genes on human chromosome 16 and Solute carrier family.
Vinony links it to 6 Wikipedia language editions.
Gene data
SLC7A5- Name
- solute carrier family 7 member 5
- Type
- protein-coding
- Position
- 87,830,016–87,869,514 (−)
- Aliases
- 4F2LC, CD98, D16S469E, E16, LAT1, MPE16
- Ensembl
- ENSG00000103257
- RefSeq RNA
- NM_003486.7
- RefSeq protein
- NP_003477.4
Enables L-leucine transmembrane transporter activity; L-tryptophan transmembrane transporter activity; and thyroid hormone transmembrane transporter activity. Involved in carboxylic acid transport; thyroid hormone transport; and xenobiotic transport. Located in cytosol; intracellular membrane-bounded organelle; and plasma membrane. Is integral component of membrane. Part of amino acid transport complex; apical plasma membrane; and microvillus membrane. [provided by Alliance of Genome Resources, Apr 2022]
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
solute carrier family 7 member 5
- Symbol
- SLC7A5
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 16:87,830,016-87,869,514
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 55759
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/8140
- genomic end
- 87869507
- genomic start
- 87863629
- chromosome
- human chromosome 16
- cytogenetic location
- 16q24.2
Sources (4)
via Wikidata · CC0