SLC38A9
Sign in to saveAlso known as URLC11, solute carrier family 38 member 9
protein-coding gene in the species Homo sapiens
Gene data
SLC38A9- Name
- solute carrier family 38 member 9
- Type
- protein-coding
- Position
- 55,621,278–55,773,194 (−)
- Aliases
- SNAT9, URLC11
- Ensembl
- ENSG00000177058
- RefSeq RNA
- NM_001258286.1, NM_001258287.1, NM_001282429.1, NM_001349382.1, NM_001349383.1
- RefSeq protein
- NP_001245215.1, NP_001245216.1, NP_001269358.1, NP_001336311.1, NP_001336312.1
Enables L-arginine transmembrane transporter activity and L-leucine transmembrane transporter activity. Involved in amino acid transmembrane transport; cellular response to amino acid stimulus; and positive regulation of TOR signaling. Located in late endosome and lysosomal membrane. Is integral component of lysosomal membrane. Colocalizes with Ragulator complex. [provided by Alliance of Genome Resources, Apr 2022]
Gene Ontology
Biological process
Molecular function
guanyl-nucleotide exchange factor activityprotein bindingamino acid transmembrane transporter activityamino acid transmembrane transporter activityL-amino acid transmembrane transporter activityL-asparagine transmembrane transporter activityL-glutamine transmembrane transporter activityL-leucine transmembrane transporter activity
Pathways
via MyGene.info
Gene · Ensembl
solute carrier family 38 member 9
- Symbol
- SLC38A9
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 5:55,621,278-55,773,194
- Strand
- Reverse (−)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 18139
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/153129
- genomic end
- 55069022
- genomic start
- 54921673
- chromosome
- human chromosome 5
- cytogenetic location
- 5q11.2
Sources (4)
via Wikidata · CC0