Symbol Name ID |
Flna
filamin, alpha MGI:95556 |
Darker colors indicate more annotations |
Human Phenotypes | Cerebral hemorrhage |
Microcephaly |
Progressive microcephaly |
Encephalocele |
Stroke |
Ectopic posterior pituitary |
Optic nerve hypoplasia |
Spastic diplegia |
Abnormal nervous system morphology |
Hydrocephalus |
Thin corpus callosum |
Partial agenesis of the corpus callosum |
Hypoplasia of the corpus callosum |
Cerebellar hypoplasia |
Chiari type I malformation |
Myelomeningocele |
Spina bifida |
Abnormality of neuronal migration |
Gray matter heterotopia |
Periventricular heterotopia |
Periventricular nodular heterotopia |
Tetraparesis |
Hypsarrhythmia |
Increased intracranial pressure |
Delayed speech and language development |
Reduced eye contact |
Diminished ability to concentrate |
Autism |
Intellectual disability |
Intellectual disability, mild |
Intellectual disability, severe |
Obstructive sleep apnea |
Gait disturbance |
Headache |
Global developmental delay |
Mild global developmental delay |
Motor delay |
Seizure |
Focal-onset seizure |
Focal motor seizure |
Infantile spasms |
Disease(s) Associated with FLNA | |||||||||||||||||||||||||||||||||||||||||
craniosynostosis | |||||||||||||||||||||||||||||||||||||||||
frontometaphyseal dysplasia 1 | |||||||||||||||||||||||||||||||||||||||||
Melnick-Needles syndrome | |||||||||||||||||||||||||||||||||||||||||
otopalatodigital syndrome type 1 | |||||||||||||||||||||||||||||||||||||||||
otopalatodigital syndrome type 2 | |||||||||||||||||||||||||||||||||||||||||
periventricular nodular heterotopia | |||||||||||||||||||||||||||||||||||||||||
X-linked cardiac valvular dysplasia | |||||||||||||||||||||||||||||||||||||||||
X-linked chronic idiopathic intestinal pseudo-obstruction |
Mouse Phenotypes | abnormal brain size |
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Availability | Mouse Genotype | |
Flnatm1.1Caw/Y H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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 09/03/2024 MGI 6.24 |
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