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XB-GENEPAGE-5799123
cc2d1a coiled-coil and C2 domain containing 1A
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (41 sources): Abnormal facial shape, Absent septum pellucidum, Autistic behavior, Cerebral atrophy, Cerebral visual impairment, Chorea, Cortical dysplasia, Delayed speech and language development, Depression, Dyskinesia, [+] |
Mouse (18 sources): abnormal brain vasculature morphology, abnormal cell morphology, abnormal dendrite morphology, abnormal excitatory postsynaptic currents, abnormal inhibitory postsynaptic currents, abnormal miniature inhibitory postsynaptic currents, abnormal neuron physiology, abnormal synaptic vesicle recycling, decreased CNS synapse formation, decreased interferon-beta secretion, [+] |
View all ortholog results at Monarch |