Obsl1 Phenotype Annotations - Multigenic Genotypes

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Obsl1
obscurin-like 1
MGI:2138628

11 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Obscn^tm1Chen/Obscn^tm1Chen Obsl1^tm1.1Slan/Obsl1^tm1.1Slan Tg(Myog-cre)1Eno/0 involves: 129 * Black Swiss * C57BL/6 * SJL	abnormal glycogen catabolism	J:283623
	abnormal mitochondrial ATP synthesis coupled electron transport	J:283623
	abnormal muscle physiology	J:283623
	abnormal sarcolemma morphology	J:283623
	abnormal sarcoplasmic reticulum morphology	J:283623
	decreased skeletal muscle enzyme/coenzyme level	J:283623
	decreased skeletal muscle fiber diameter	J:283623
	increased catalase level	J:283623
	normal mortality/aging	J:283623
	normal muscle phenotype	J:283623
	normal reproductive system phenotype	J:283623

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