Obscn Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Obscn
obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF
MGI:2681862

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 enzyme/coenzyme level	J:283623
	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 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)
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