Slc17a9 - solute carrier family 17 member 9 Gene

Rattus norvegicus

Also known as RGD1311940

Gene ID: 362287 | Gene type: protein coding

About Slc17a9

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	Reference	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

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

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