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 |
|
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) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 08/21/2024 MGI 6.24 |
![]() |
|