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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 |
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| 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 05/07/2024 MGI 6.23 |
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