|
Symbol Name ID |
Nfia
nuclear factor I/A MGI:108056 |
| Darker colors indicate more annotations |
| Human Phenotypes | Intraventricular hemorrhage |
Moyamoya phenomenon |
Ventriculomegaly |
Aplasia/Hypoplasia of the corpus callosum |
Agenesis of corpus callosum |
Hypoplasia of the corpus callosum |
Chiari type I malformation |
Tethered cord |
Syringomyelia |
Attention deficit hyperactivity disorder |
Compulsive behaviors |
Cognitive impairment |
Intellectual disability |
Global developmental delay |
Delayed fine motor development |
Delayed gross motor development |
Seizure |
| Disease(s) Associated with NFIA | |||||||||||||||||
| NFIA-related disorder |
| Mouse Phenotypes | abnormal glial cell morphology |
abnormal axon extension |
abnormal cerebellar foliation |
hydrocephaly |
dilated lateral ventricle |
dilated third ventricle |
abnormal corpus callosum morphology |
absent corpus callosum |
abnormal hippocampal commissure morphology |
abnormal hippocampus morphology |
abnormal cerebellar granule cell morphology |
abnormal cerebellar molecular layer |
syringomyelia |
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| Availability | Mouse Genotype | |||||||||||||
| Nfiatm1Rmg/Nfiatm1Rmg | ||||||||||||||
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 03/31/2026 MGI 6.24 |
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