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Symbol Name ID |
Stil
Scl/Tal1 interrupting locus MGI:107477 |
| Darker colors indicate more annotations |
| Human Phenotypes | Primary microcephaly |
Simplified gyral pattern |
Absent speech |
Intellectual disability |
Intellectual disability, severe |
Global developmental delay |
Seizure |
| Disease(s) Associated with STIL | |||||||
| primary autosomal recessive microcephaly 7 |
| Mouse Phenotypes | abnormal neural tube morphology |
absent floor plate |
delayed neural tube closure |
holoprosencephaly |
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| Availability | Mouse Genotype | ||||
| Stiltm1Mku/Stiltm1Mku | |||||
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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