fbxo31 Phenotypes

Phenotypes

XB-GENEPAGE-953634

Gene Symbol: fbxo31 Gene Name: F-box protein 31

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: fbxo31 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (38 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-onset seizure, Generalized hypotonia, Generalized-onset seizure, Global developmental delay, Hyperactivity, Hypoplasia of the corpus callosum, Hypotonia, Hypsarrhythmia, Impulsivity, 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 disturbance, Spasticity [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Human (38 sources): Abnormal facial shape, Absent septum pellucidum, Autistic behavior, Cerebral atrophy, Cerebral visual impairment, Chorea, Cortical dysplasia, Delayed speech and language development, Depression, Dyskinesia, [+]