med23 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (124)

Interactants (57)

XB-GENEPAGE-1003993

Gene Symbol: med23 Gene Name: mediator complex subunit 23

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (39 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, 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 [+]
Mouse (18 sources): abnormal cell differentiation, abnormal chorion morphology, abnormal nervous system development, abnormal placenta morphology, abnormal trigeminal ganglion morphology, abnormal trophoblast giant cell morphology, abnormal trophoblast layer morphology, abnormal vascular development, absent second pharyngeal arch, decreased embryo size, embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance, impaired cranial neural crest cell differentiation, lethality throughout fetal growth and development, complete penetrance, no abnormal phenotype detected, preweaning lethality, complete penetrance, second pharyngeal arch hypoplasia, small frontonasal prominence [+]
View all ortholog results at Monarch