Symbol Name ID |
Emilin1
elastin microfibril interfacer 1 MGI:1926189 |
Darker colors indicate more annotations |
Human Phenotypes | Bruising susceptibility |
Disease(s) Associated with EMILIN1 | |
autosomal dominant distal hereditary motor neuronopathy 10 |
Mouse Phenotypes | decreased platelet aggregation |
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Availability | Mouse Genotype | |
Emilin1tm1Gmb/Emilin1tm1Gmb |
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 05/14/2024 MGI 6.23 |
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