|
Symbol Name ID |
Camta1
calmodulin binding transcription activator 1 MGI:2140230 |
| Darker colors indicate more annotations |
| Human Phenotypes | Drooling |
Cerebral cortical atrophy |
Hippocampal atrophy |
Cerebellar hypoplasia |
Ataxia |
Dysmetria |
Gait ataxia |
Poor gross motor coordination |
Hand tremor |
Delayed speech and language development |
Dysarthria |
Aggressive behavior |
Hyperactivity |
Attention deficit hyperactivity disorder |
Motor stereotypy |
Intellectual disability |
Intellectual disability, mild |
Broad-based gait |
Unsteady gait |
Global developmental delay |
Seizure |
Bilateral tonic-clonic seizure |
Generalized myoclonic-atonic seizure |
| Disease(s) Associated with CAMTA1 | |||||||||||||||||||||||
| nonprogressive cerebellar ataxia with mental retardation |
| Mouse Phenotypes | abnormal Purkinje cell morphology |
Purkinje cell degeneration |
thin cerebellar granule layer |
thin cerebellar molecular layer |
cerebellum atrophy |
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| Availability | Mouse Genotype | |||||
| Camta1tm1.1Eno/Camta1tm1.1Eno Tg(Nes-cre)1Kln/0 (conditional) |
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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 04/30/2024 MGI 6.23 |
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