|Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 7
expressed sequence AI790233,
| Description: PHENOTYPE: Homozygous null mice exhibit fetal growth retardation and often die neonatally. After heavy protein ingestion, surviving adults show a metabolic derangement akin to lysinuric protein intolerance and including a lasting postnatal growth retardation, splenomegaly, hyperammonemia, and aminoaciduria. [provided by MGI curators]
|This information is supplied by the AllianceGenome.org API.