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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Obscntm1Chen/Obscntm1Chen
Obsl1tm1.1Slan/Obsl1tm1.1Slan
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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory