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Symbol Name ID |
Supt16
SPT16, facilitates chromatin remodeling subunit MGI:1890948 |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties |
Autistic behavior |
| Disease(s) Associated with SUPT16H | ||
| neurodevelopmental disorder with dysmorphic facies and thin corpus callosum |
| Mouse Phenotypes | abnormal object recognition memory |
impaired spatial learning |
abnormal spatial reference memory |
increased thigmotaxis |
decreased social novelty preference |
decreased social investigation |
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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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