Definition
any functional anomaly of the eye as determined through electrophysiological recordings from single cells or summary recordings from multiple cells (e.g. electroretinogram)
0%
of tested genes
0
significant genes
0
tested genes
IMPC Gene variants with abnormal eye electrophysiology
Total number of significant genotype-phenotype associations: 1
| Gene / Allele | Zygosity | Sex | Life Stage | Phenotype | Parameter | Phenotyping Center |
P Value |
|---|---|---|---|---|---|---|---|
| Dll1 Dll1tm1Gos |
HET | Early adult | abnormal eye electrophysiology | B-Wave 12500 Cd/m² right eye ERG (Electroretinogram) (GMC) |
HMGU EuroPhenome |
8.34×10-05 |