Human Disease and Mouse Model Detail
|
Human Disease
|
Axenfeld-Rieger Syndrome, Type 3; RIEG3
OMIM ID: 602482
|
|
Synonyms
|
Anterior Chamber Cleavage Syndrome;
Anterior Segment Mesenchymal Dysgenesis;
Axenfeld-Rieger Anomaly with or without Cardiac Defects and/or Sensorineural Hearing Loss
|
|
View all models
|
View ALL (1) mouse models for this human disease.
|
Genes and
mouse models
|
Mutations in human and/or mouse homologs are associated with this disease
| |
|
|
*Gene is associated with the disease in this species |
| |
|
|
 | | |
Bmp4*
|
BMP4
|
View 1 model
|
1:1 Homology
|
 | | |
Foxc1
|
FOXC1*
|
|
1:1 Homology
|
|
Mouse Models
Human Disease Modeled: Axenfeld-Rieger Syndrome, Type 3; RIEG3
Associated Mouse Gene:
Bmp4
Analysis Tools