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 |
Compulsive behaviors |
Attention deficit hyperactivity disorder |
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 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 |
abnormal glial cell morphology |
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 05/07/2024 MGI 6.23 |
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