fmn2 Phenotypes

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Phenotypes

Gene Literature (8)

Nucleotides (86)

Interactants (191)

XB-GENEPAGE-5955924

Gene Symbol: fmn2 Gene Name: formin 2

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (40 sources): Abnormal facial shape, Absent septum pellucidum, Autistic behavior, Cerebral atrophy, Cerebral visual impairment, Chorea, Cortical dysplasia, Delayed speech and language development, Depression, Dyskinesia, Dystonia, EEG with focal epileptiform discharges, EEG with generalized epileptiform discharges, Epileptic spasm, Focal impaired awareness seizure, Focal-onset seizure, Generalized hypotonia, Generalized-onset seizure, Global developmental delay, Hyperactivity, Hypoplasia of the corpus callosum, Hypotonia, Hypsarrhythmia, Impulsivity, Intellectual disability, Intellectual disability, mild, Intellectual disability, moderate, Intellectual disability, severe, Large basal ganglia, Microcephaly, Motor delay, Motor stereotypy, Multifocal epileptiform discharges, Nasogastric tube feeding, Polymicrogyria, Poor speech, Seizure, Short attention span, Sleep abnormality, Spasticity [+]
Mouse (6 sources): abnormal female meiosis, abnormal nursing, abnormal oocyte morphology, abnormal pregnancy, abnormal primary polar body morphology, reduced female fertility
View all ortholog results at Monarch