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
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