Disease-gene associations mined from literature

Literature associating SLC7A1 and amelogenesis imperfecta type 1G

SLC7A1 [ENSP00000370128]

Solute carrier family 7 (cationic amino acid transporter, y+ system), member 1; High-affinity, low capacity permease involved in the transport of the cationic amino acids (arginine, lysine and ornithine) in non-hepatic tissues; Belongs to the amino acid-polyamine-organocation (APC) superfamily. Cationic amino acid transporter (CAT) (TC 2.A.3.3) family.

Synonyms:  SLC7A1,  SLC7A1p,  hSLC7A1,  A0A024RDQ9,  P30825 ...

Linkouts:  STRING  Pharos  UniProt  OMIM