Slc7a14 - solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 Gene

Also Known as A930013N06

Species: Mus musculus

Gene Type: protein coding
Gene ID: 241919

Summary

Predicted to enable amino acid transmembrane transporter activity. Predicted to be involved in amino acid transport. Predicted to be located in cytosol and nucleoplasm. Predicted to be active in plasma membrane. Is expressed in several structures, including central nervous system; eye; and pancreas trunk epithelium. Human ortholog(s) of this gene implicated in retinitis pigmentosa 68. Orthologous to human SLC7A14 (solute carrier family 7 member 14). [provided by Alliance of Genome Resources, Apr 2022]

Slc7a14 Products (1)

mRNA Protein Name
NM_172861.3 NP_766449.1 probable cationic amino acid transporter

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables gamma-aminobutyric acid transmembrane transporter activity IDA
IDA: Inferred from direct assay
36640347 MGI
Biological Process GO Annotation Evidence References Source
involved in gamma-aminobutyric acid import IMP
IMP: Inferred from mutant phenotype
36640347 MGI
Cellular Component GO Annotation Evidence References Source
located in lysosomal membrane IDA
IDA: Inferred from direct assay
36640347 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

probable cationic amino acid transporter

  • solute carrier family 7, member 14

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13327 SLC7A14 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc7a14 NCBI NCBI:57709