Ocm Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 09/30/2025 MGI 6.24