| Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 |
| Aliases:
AI790233,
my+lat1,
y+LAT1,
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] |
| Crossreferences:
MGI:1337120,
UniProtKB:Q9Z1K8,
NCBI_Gene:20540,
UniProtKB:A0A0G2JE10,
UniProtKB:A0A2I3BQX2,
UniProtKB:A0A2I3BPU1,
UniProtKB:A0A0G2JEB8,
UniProtKB:A0A0G2JEM2,
ENSEMBL:ENSMUSG00000000958,
UniProtKB:A0A2I3BQK2
|
| This information is supplied by the AllianceGenome.org API. |