Ocm Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ocm
oncomodulin
MGI:97401

9 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ocm^tm1.1Ddsi/Ocm^tm1.1Ddsi involves: 129X1/SvJ * CBA/CaJ * FVB/N	deafness	J:153876
Ocm^tm1.1Ddsi/Ocm^tm1.1Ddsi involves: 129X1/SvJ * FVB/N	abnormal distortion product otoacoustic emission	J:231626
	cochlear inner hair cell degeneration	J:231626
	cochlear outer hair cell degeneration	J:231626
	decreased threshold for auditory brainstem response	J:231626
	impaired hearing	J:231626
	increased or absent threshold for auditory brainstem response	J:231626
	pillar cell degeneration	J:231626
Ocm^{tm1e(EUCOMM)Wtsi}/Ocm^{tm1e(EUCOMM)Wtsi} C57BL/6N-Ocm^{tm1e(EUCOMM)Wtsi}/Wtsi	absent pinna reflex	J:211773

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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