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Symbol Name ID |
Serac1
serine active site containing 1 MGI:2447813 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spasticity |
Cerebellar atrophy |
Brain atrophy |
Aplasia/Hypoplasia involving the central nervous system |
Abnormality of extrapyramidal motor function |
Absent speech |
Intellectual disability |
Dystonia |
Inability to walk |
Encephalopathy |
Developmental regression |
Global developmental delay |
Seizure |
| Disease(s) Associated with SERAC1 | ||||||||||||||
| 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome |
| Mouse Phenotypes | abnormal basal ganglion morphology |
brain lesion |
encephalopathy |
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| Availability | Mouse Genotype | |||
| Serac1em1Bcgen/Serac1em1Bcgen | ||||
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 05/28/2024 MGI 6.13 |
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