Abhd12 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Abhd12
abhydrolase domain containing 12
MGI:1923442

13 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Abhd12^tm1Crv/Abhd12^tm1Crv involves: C57BL/6	abnormal phospholipid level	J:193716
	absent startle reflex	J:193716
	ataxia	J:193716
	decreased lipoprotein lipase activity	J:193716
	decreased startle reflex	J:193716
	hyperactivity	J:193716
	impaired coordination	J:193716
	impaired hearing	J:193716
	increased auditory brainstem response wave interpeak latency	J:193716
	increased auditory brainstem response wave peak latency	J:193716
	microgliosis	J:193716
	muscle weakness	J:193716
	normal vision/eye phenotype	J:193716

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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