Ugt8a Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ugt8a
UDP galactosyltransferase 8A
MGI:109522

18 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ugt8a^tm1Pop/Ugt8a⁺ involves: 129P2/OlaHsd * C57BL/6	abnormal lipid level	J:77226
Ugt8a^tm1Pop/Ugt8a^tm1Pop involves: 129P2/OlaHsd	abnormal Purkinje cell axon morphology	J:107653
Ugt8a^tm1Pop/Ugt8a^tm1Pop involves: 129P2/OlaHsd	abnormal Purkinje cell morphology	J:107653
Ugt8a^tm1Pop/Ugt8a^tm1Pop involves: 129P2/OlaHsd * C57BL/6	abnormal head movements	J:77226
	abnormal lipid level	J:77226
	abnormal myelination	J:78426
	abnormal nerve conduction	J:58935, J:78426
	ataxia	J:77226
	decreased body weight	J:77226
	hindlimb paralysis	J:77226
	normal immune system phenotype	J:78426
	normal nervous system phenotype	J:78426
	premature death	J:77226
	tremors	J:77226
Ugt8a^tm1Wst/Ugt8a^tm1Wst involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal gait	J:36558
	abnormal lipid level	J:36558
	abnormal nerve conduction	J:36558
	decreased locomotor activity	J:36558
	demyelination	J:36558, J:48209
	forelimb paralysis	J:36558
	hindlimb paralysis	J:36558
	postnatal growth retardation	J:36558
	premature death	J:36558
	tremors	J:36558

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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