Symbol Name ID |
Slc7a1
solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 MGI:88117 |
Allelic Composition Genetic Background |
Annotated Term | Reference |
Slc7a1tm1Rbmn/Slc7a1tm1Rbmn either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: C57BL/6) |
abnormal cell physiology | J:39649 |
abnormal proerythroblast morphology | J:39649 | |
abnormal reticulocyte morphology | J:39649 | |
anemia | J:39649 | |
anisopoikilocytosis | J:39649 | |
decreased body size | J:39649 | |
decreased body weight | J:39649 | |
decreased erythrocyte cell number | J:39649 | |
decreased hemoglobin content | J:39649 | |
decreased mean corpuscular hemoglobin | J:39649 | |
increased nucleated erythrocyte cell number | J:39649 | |
neonatal lethality, complete penetrance | J:39649 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 12/17/2024 MGI 6.24 |
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