Symbol Name ID |
Obsl1
obscurin-like 1 MGI:2138628 |
Darker colors indicate more annotations |
Human Phenotypes | Short 5th finger |
Clinodactyly of the 5th finger |
Clinodactyly |
Rocker bottom foot |
Prominent calcaneus |
Abnormal metaphysis morphology |
Hypoplasia of the ulna |
Pes planus |
Hip dislocation |
Congenital hip dislocation |
Scapular winging |
Abnormality of the elbow |
Micromelia |
Disease(s) Associated with OBSL1 | |||||||||||||
3-M syndrome |
Mouse Phenotypes | increased extensor digitorum longus weight |
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Availability | Mouse Genotype | |
Obsl1tm1.1Slan/Obsl1tm1.1Slan Tg(Myog-cre)1Eno/0 (conditional) |
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 09/03/2024 MGI 6.24 |
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