Symbol Name ID |
Mccc2
methylcrotonoyl-Coenzyme A carboxylase 2 (beta) MGI:1925288 |
Darker colors indicate more annotations |
Human Phenotypes | Opisthotonus |
Cerebral palsy |
Lethargy |
Intellectual disability |
Coma |
Hyperreflexia |
Global developmental delay |
Seizure |
Disease(s) Associated with MCCC2 | ||||||||
3-methylcrotonyl-CoA carboxylase 2 deficiency |
Mouse Phenotypes | increased prepulse inhibition |
|
Availability | Mouse Genotype | |
Mccc2em1(IMPC)J/Mccc2+ |
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 08/02/2024 MGI 6.24 |
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