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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc7a1
solute carrier family 7 (cationic amino acid transporter, y+ system), member 1
MGI:88117
12 phenotypes from 1 allele in 1 genetic background
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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

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/09/2019
MGI 6.13
The Jackson Laboratory