Slc7a1 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Slc7a1^tm1Rbmn/Slc7a1^tm1Rbmn 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

Contributing Projects: 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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