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abnormal midbrain morphology

12

significant genes

1.74%

of tested genes

691

tested genes

Description

any structural anomaly associated with the brain region derived from the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions in the adult, including eye movement and coordination of auditory and visual reflexes

Significant gene-phenotype associationsView data

IMPC Gene variants with abnormal midbrain morphology

Number of significant genotype-phenotype associations: 0












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Most significant associations for abnormal midbrain morphology

  Not significant  Significant  Manual associations

  Significant P-Value threshold (P < 0.0001)
Associations appearing in the region of 1x10-30 are manually annotated as significant.

Associations details of selected gene(s):

Click on a point of the chart to see the details of an association.

The way we measure

Procedure

Gross Morphology Embryo E12.5