| Monarch Ortholog Phenotypes
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Human (13 sources):
Agyria,
Cortical dysplasia,
Global developmental delay,
Gray matter heterotopia,
Hypoplasia of the corpus callosum,
Intrauterine growth retardation,
Lissencephaly,
Microcephaly,
Nystagmus,
Pachygyria,
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Mouse (12 sources):
abnormal axon extension,
abnormal axon morphology,
abnormal hippocampus layer morphology,
abnormal inferior olivary complex morphology,
abnormal nervous system development,
abnormal pons morphology,
abnormal pontine nuclei morphology,
abnormal stratification in cerebral cortex,
abnormal suckling behavior,
abnormal tegmentum morphology,
[+]
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View all ortholog results at Monarch
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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.