Symbol Name ID |
Nedd4l
neural precursor cell expressed, developmentally down-regulated gene 4-like MGI:1933754 |
Darker colors indicate more annotations |
Human Phenotypes | Cerebral hemorrhage |
Microcephaly |
Progressive microcephaly |
Stroke |
Abnormal nervous system morphology |
Thin corpus callosum |
Hypoplasia of the corpus callosum |
Cerebellar hypoplasia |
Abnormality of neuronal migration |
Gray matter heterotopia |
Periventricular heterotopia |
Periventricular nodular heterotopia |
Tetraparesis |
Hypsarrhythmia |
Reduced eye contact |
Delayed speech and language development |
Intellectual disability |
Intellectual disability, mild |
Intellectual disability, severe |
Global developmental delay |
Mild global developmental delay |
Seizure |
Focal-onset seizure |
Focal motor seizure |
Infantile spasms |
Disease(s) Associated with NEDD4L | |||||||||||||||||||||||||
periventricular nodular heterotopia |
Mouse Phenotypes | decreased prepulse inhibition |
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Availability | Mouse Genotype | |
Nedd4ltm1b(KOMP)Wtsi/Nedd4ltm1b(KOMP)Wtsi |
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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