|
Symbol Name ID |
Supt16
SPT16, facilitates chromatin remodeling subunit MGI:1890948 |
| Darker colors indicate more annotations |
| Human Phenotypes | Unilateral facial palsy |
Torticollis |
Thin corpus callosum |
Partial agenesis of the corpus callosum |
Spina bifida |
Tethered cord |
Absent speech |
Delayed speech and language development |
Autistic behavior |
Intellectual disability |
Sleep abnormality |
Global developmental delay |
Delayed gross motor development |
Focal impaired awareness seizure |
Focal aware seizure |
| Disease(s) Associated with SUPT16H | |||||||||||||||
| neurodevelopmental disorder with dysmorphic facies and thin corpus callosum |
| Mouse Phenotypes | abnormal dendrite morphology |
decreased dendritic spine density |
decreased dendritic spine length |
decreased dendritic spine number |
decreased neuron number |
abnormal nervous system electrophysiology |
abnormal neuronal stem cell physiology |
decreased neuronal stem cell self-renewal |
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| Availability | Mouse Genotype | ||||||||
| Supt16em1Hguo/Supt16+ | |||||||||
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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