Slc7a9 - solute carrier family 7 member 9 Gene

Rattus norvegicus

Gene ID: 116726 | Gene type: protein coding

About Slc7a9

Summary

Enables amino acid transmembrane transporter activity. Involved in amino acid transport. Located in plasma membrane. Human ortholog(s) of this gene implicated in cystinuria. Orthologous to human SLC7A9 (solute carrier family 7 member 9). [provided by Alliance of Genome Resources, Apr 2022]

Slc7a9 Products(1)

mRNA	Protein	Name
NM_053929.1	NP_446381.1	B(0,+)-type amino acid transporter 1

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables amino acid transmembrane transporter activity	IDA IDA: Inferred from direct assay	10506124	RGD

Biological Process GO Annotation	Evidence	Reference	Source
involved in amino acid transport	IDA IDA: Inferred from direct assay	10506124	RGD

Cellular Component GO Annotation	Evidence	Reference	Source
located in plasma membrane	IDA IDA: Inferred from direct assay	16358225	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

B(0,+)-type amino acid transporter 1

b(0,+)AT	glycoprotein-associated amino acid transporter b0,+AT1
solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9	solute carrier family 7 (cationic amino acid transporter, y+ system), member 9
solute carrier family 7

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13336	SLC7A9 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Slc7a9	NCBI	NCBI:11136

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