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FLASH GENE
Symbol SLC7A2 contributors: mct/npt/pgu - updated : 31-10-2013
HGNC name solute carrier family 7 (cationic amino acid transporter, y+ system), member 2
HGNC id 11060
ASSOCIATED DISORDERS
corresponding disease(s)
Susceptibility
Variant & Polymorphism SNP
  • a single-nucleotide variation in the first intron of the SLC7A2 gene (IVS1-1713 A > G) associated to infantile encephalopathy with severe infantile anorexia
  • Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS
  • Cat2(-/-) mice are significantly more susceptible to the Th1-inducing pathogen Toxoplasma gondii