SLC38A10
Sign in to saveAlso known as PP1744, solute carrier family 38 member 10
protein-coding gene in the species Homo sapiens
Gene data
SLC38A10- Name
- solute carrier family 38 member 10
- Type
- protein-coding
- Position
- 81,244,811–81,295,567 (−)
- Aliases
- PP1744, SNAT10
- Ensembl
- ENSG00000157637
- RefSeq RNA
- NM_001037984.3, NM_138570.4, XM_005257019.2, XM_011524288.2, XM_011524289.2
- RefSeq protein
- NP_001033073.1, NP_612637.1, XP_005257076.1, XP_011522590.1, XP_011522591.1
Predicted to enable amino acid transmembrane transporter activity. Predicted to be involved in amino acid transmembrane transport. Predicted to act upstream of or within bone development. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Apr 2022]
Gene Ontology
Molecular function
Cellular component
via MyGene.info
Gene · Ensembl
solute carrier family 38 member 10
- Symbol
- SLC38A10
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 17:81,244,811-81,295,567
- Strand
- Reverse (−)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 41556
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/124565
- genomic end
- 79269347
- genomic start
- 81244811
- chromosome
- human chromosome 17
- cytogenetic location
- 17q25.3
- expressed in
- granulocyte
Sources (3)
via Wikidata · CC0