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MGP Database

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MGP002877

Ontology/Pathway Information

Entrez Gene ID	6542
Gene Name	solute carrier family 7 (cationic amino acid transporter, y+ system), member 2
Gene Symbol	SLC7A2
Species	Homo sapiens

Gene Ontology (GO Annotations)

GO ID	Source	Type	Description
GO:0005887	TAS:ProtInc	C	integral component of plasma membrane
GO:0016020	TAS:ProtInc	C	membrane
GO:0005886	TAS:Reactome	C	plasma membrane
GO:0015174	TAS:ProtInc	F	basic amino acid transmembrane transporter activity
GO:0005289	IEA:Ensembl	F	high-affinity arginine transmembrane transporter activity
GO:0015189	IEA:Ensembl	F	L-lysine transmembrane transporter activity
GO:0000064	IEA:Ensembl	F	L-ornithine transmembrane transporter activity
GO:0006865	TAS:Reactome	P	amino acid transport
GO:0006520	TAS:ProtInc	P	cellular amino acid metabolic process
GO:0006811	TAS:Reactome	P	ion transport
GO:0042116	IEA:Ensembl	P	macrophage activation
GO:0006809	IEA:Ensembl	P	nitric oxide biosynthetic process
GO:0002537	IEA:Ensembl	P	nitric oxide production involved in inflammatory response
GO:0050727	IEA:Ensembl	P	regulation of inflammatory response
GO:0043030	IEA:Ensembl	P	regulation of macrophage activation
GO:0055085	TAS:Reactome	P	transmembrane transport
GO:0006810	TAS:ProtInc	P	transport

SMP Pathway Links

SMP ID	Description
SMP00719	2-aminoadipic 2-oxoadipic aciduria
SMP00186	Glutaric Aciduria Type III
SMP00527	Hyperlysinemia I, Familial
SMP00528	Hyperlysinemia II or Saccharopinuria
SMP00037	Lysine Degradation
SMP00571	Pyridoxine dependency with seizures
SMP00239	Saccharopinuria/Hyperlysinemia II