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Symbol
Name
ID
Obsl1
obscurin-like 1
MGI:2138628
Phenotype annotations related to muscle
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Scapular winging
Disease(s) Associated with OBSL1
3-M syndrome

Mouse Phenotypes
muscle phenotype
increased extensor digitorum longus weight
increased skeletal muscle fiber diameter
Availability Mouse Genotype
Obsl1tm1.1Slan/Obsl1tm1.1Slan
Tg(Myog-cre)1Eno/0  (conditional)
*

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
04/16/2024
MGI 6.23
The Jackson Laboratory