|
Symbol Name ID |
Cad
carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase MGI:1916969 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dysphagia |
Global brain atrophy |
Poor speech |
Broad-based gait |
Epileptic encephalopathy |
Developmental regression |
Global developmental delay |
Seizure |
Status epilepticus |
| Disease(s) Associated with CAD | |||||||||
| developmental and epileptic encephalopathy 50 |
| Mouse Phenotypes | decreased prepulse inhibition |
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| Availability | Mouse Genotype | |
| Cadem1(IMPC)Mbp/Cad+ | ||
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 04/23/2024 MGI 6.23 |
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