chrdl1 chordin-like 1
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
|Human (14 sources): Astigmatism, Cataract, Corneal arcus, Decreased corneal thickness, Deep anterior chamber, Glaucoma, Iridodonesis, Iris transillumination defect, Lens subluxation, Megalocornea, [+]|
|Mouse (4 sources): abnormal miniature excitatory postsynaptic currents, abnormal synapse morphology, abnormal synaptic plasticity, increased fasting circulating glucose level|
View all ortholog results at Monarch