Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 |
Aliases: AI790233, my+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:A0A0G2JEM2, UniProtKB:A0A0G2JEB8, UniProtKB:A0A2I3BQK2, UniProtKB:A0A2I3BPU1, ENSEMBL:ENSMUSG00000000958, UniProtKB:A0A2I3BQX2, UniProtKB:Q9Z1K8, UniProtKB:A0A0G2JE10, NCBI_Gene:20540 |
This information is supplied by the AllianceGenome.org API. |
Compared To: | Log2fold: | SEM: | Adjusted p-value: |
---|---|---|---|
EV-GFPneg Tumor Microglia | -0.078 | 0.269 | 1 |
EV-GFPpos Tumor Microglia | 0.989 | 0.271 | 0.00288279 |
Compared To: | Log2fold: | SEM: | Adjusted p-value: |
---|---|---|---|
Control microglia | 0.078 | 0.269 | 1 |
EV-GFPpos Tumor Microglia | 1.067 | 0.271 | 0.00342875 |
Compared To: | Log2fold: | SEM: | Adjusted p-value: |
---|---|---|---|
Control Microglia | -0.989 | 0.271 | 0.00288279 |
EV-GFPneg Tumor Microglia | -1.067 | 0.271 | 0.00342875 |