| Monarch Ortholog Phenotypes
|
Human (50 sources):
Abnormal eating behavior,
Abnormal social behavior,
Aggressive behavior,
Anxiety,
Ataxia,
Atonic seizure,
Atypical absence seizure,
Atypical absence status epilepticus,
Autistic behavior,
Behavioral abnormality,
Bilateral tonic-clonic seizure,
Bilateral tonic-clonic seizure with focal onset,
Cerebral atrophy,
Cerebral visual impairment,
Complex febrile seizure,
Compulsive behaviors,
Cutaneous photosensitivity,
Delayed speech and language development,
Developmental regression,
EEG abnormality,
Epileptic encephalopathy,
Febrile seizure (within the age range of 3 months to 6 years),
Focal clonic seizure,
Focal hemiclonic seizure,
Focal impaired awareness seizure,
Focal-onset seizure,
Generalized clonic seizure,
Generalized myoclonic seizure,
Generalized non-motor (absence) seizure,
Generalized tonic seizure,
Generalized-onset seizure,
Global developmental delay,
Hyperactivity,
Hypotonia,
Impulsivity,
Intellectual disability,
Intellectual disability, mild,
Intellectual disability, moderate,
Intellectual disability, profound,
Intellectual disability, severe,
Mental deterioration,
Motor delay,
Neurodevelopmental delay,
Psychomotor retardation,
Psychosis,
Secondary microcephaly,
Seizure,
Status epilepticus,
Tremor,
obsolete Focal seizures, afebril
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Mouse (4 sources):
abnormal brain wave pattern,
abnormal forebrain development,
behavior/neurological phenotype,
nervous system phenotype
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View all ortholog results at Monarch
|
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.