Definition
anomaly in the process by which the upper and lower eyelids are joined during development
Synonyms
abnormal palpenrae fusion,
abnormal eye lid fusion,
abnormal blephara fusion,
abnormal palpebra fusion,
abnormal blepharon fusion
0%
of tested genes
0
significant genes
0
tested genes
IMPC Gene variants with abnormal eyelid fusion
Total number of significant genotype-phenotype associations: 7
| Gene / Allele | Zygosity | Sex | Life Stage | Phenotype | Parameter | Phenotyping Center |
P Value |
|---|---|---|---|---|---|---|---|
| Axin2 Axin2tm1b(KOMP)Wtsi |
HOM | E18.5 | abnormal eyelid fusion | Failure of Eyelid Fusion Gross Morphology Embryo E18.5 |
BCM IMPC |
0.00 | |
| Bcl11b Bcl11btm1.1(KOMP)Vlcg |
HOM | E18.5 | abnormal eyelid fusion | Failure of Eyelid Fusion Gross Morphology Embryo E18.5 |
JAX IMPC |
0.00 | |
| Tmem209 Tmem209em1(IMPC)Tcp |
HOM | E18.5 | abnormal eyelid fusion | Failure of Eyelid Fusion Gross Morphology Embryo E18.5 |
TCP IMPC |
0.00 | |
| Ubn2 Ubn2em1(IMPC)Tcp |
HOM | E18.5 | abnormal eyelid fusion | Failure of Eyelid Fusion Gross Morphology Embryo E18.5 |
TCP IMPC |
0.00 |