ywhag Phenotypes

Phenotypes

XB-GENEPAGE-951349

Gene Symbol: ywhag Gene Name: tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (54 sources): Abnormal corpus callosum morphology, Abnormal involuntary eye movements, Abnormality of coordination, Abnormality of vision, Abnormal myelination, Anxiety, Ataxia, Attention deficit hyperactivity disorder, Atypical behavior, Autism, Brain atrophy, Broad-based gait, Cerebral atrophy, Decreased fetal movement, Delayed speech and language development, Developmental regression, Downslanted palpebral fissures, Dyskinesia, EEG abnormality, EEG with multifocal slow activity, Encephalopathy, Failure to thrive, Feeding difficulties, Gastroesophageal reflux, Generalized hypotonia, Global developmental delay, High forehead, Hypodontia, Hyporeflexia, Hypsarrhythmia, Impulsivity, Intellectual disability, Involuntary movements, Limb hypertonia, Mental deterioration, Microcephaly, Myoclonus, Nystagmus, Obsessive-compulsive trait, obsolete Difficulty walking, Optic atrophy, Poor coordination, Poor head control, Ptosis, Reduced tendon reflexes, Retinal degeneration, Rigidity, Scoliosis, Seizure, Short stature, Spasticity, Status epilepticus, Tremor, Unsteady gait [+]
Mouse (1 source): no abnormal phenotype detected
View all ortholog results at Monarch