|
Symbol Name ID |
Actl6b
actin-like 6B MGI:1933548 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Lower limb spasticity |
Upper limb spasticity |
Delayed CNS myelination |
Hypoplasia of the corpus callosum |
Periventricular white matter hyperintensities |
Cerebral atrophy |
Cerebellar atrophy |
Multifocal epileptiform discharges |
Absent speech |
Intellectual disability |
Inability to walk |
Severe global developmental delay |
Seizure |
| Disease(s) Associated with ACTL6B | ||||||||||||||
| developmental and epileptic encephalopathy 76 |
| Mouse Phenotypes | decreased CNS synapse formation |
abnormal dendrite morphology |
abnormal myelination |
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| Availability | Mouse Genotype | |||
| Actl6btm1Grc/Actl6btm1Grc | ||||
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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