Slc51a Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc51a
solute carrier family 51, alpha subunit
MGI:2146634

8 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc51a^tm1Nbal/Slc51a^tm1Nbal involves: C57BL/6	postnatal growth retardation	J:126544
Slc51a^tm1Pda/Slc51a^tm1Pda involves: 129S6/SvEvTac * C57BL/6J	abnormal bile salt homeostasis	J:132778
	abnormal bile salt level	J:132778
	abnormal cholesterol level	J:132778
	abnormal feces composition	J:132778
	abnormal small intestine morphology	J:132778
	decreased circulating cholesterol level	J:132778
	decreased circulating triglyceride level	J:132778
	postnatal growth retardation	J:132778

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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