no spontaneous movement

100

significant genes

31.55%

of tested genes

317

tested genes

Description

failure of neonates or embryos to initiate any voluntary or spontaneous change in position or posture, with or without external stimulus

Significant gene-phenotype associationsView data

IMPC Gene variants with no spontaneous movement

Total number of significant genotype-phenotype associations: 0










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Most significant associations for no spontaneous movement

  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 E18.5

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