Slc17a9 - solute carrier family 17 member 9 Gene

Also Known as RGD1311940

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 362287

Summary

Predicted to enable ADP transmembrane transporter activity; ATP transmembrane transporter activity; and guanine nucleotide transmembrane transporter activity. Acts upstream of or within ATP export. Predicted to be located in chromaffin granule membrane. Human ortholog(s) of this gene implicated in porokeratosis. Orthologous to human SLC17A9 (solute carrier family 17 member 9). [provided by Alliance of Genome Resources, Apr 2022]

Slc17a9 Products (1)

mRNA Protein Name
NM_001108613.1 NP_001102083.1 solute carrier family 17 member 9

Gene Ontology

  • Biological Process
Biological Process GO Annotation Evidence References Source
acts upstream of or within ATP export IMP
IMP: Inferred from mutant phenotype
18375752 RGD
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

solute carrier family 17 member 9

  • solute carrier family 17 (vesicular nucleotide transporter), member 9

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13042 SLC17A9 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc17a9 NCBI NCBI:63910