| Monarch Ortholog Phenotypes
|
Human (23 sources):
Accessory spleen,
Ambiguous genitalia,
Aplasia of the uterus,
Atrial septal defect,
Bifid scrotum,
Bronchomalacia,
Cryptorchidism,
Delayed speech and language development,
Dextrocardia,
Dysplastic tricuspid valve,
Hepatopulmonary fusion,
Hypoplastic left heart,
Intellectual disability,
Intestinal malrotation,
Micropenis,
Motor delay,
Patent ductus arteriosus,
Patent urachus,
Pulmonary hypoplasia,
Scimitar anomaly,
Seizure,
Tetralogy of Fallot,
Ventricular septal defect
[+]
|
|
Mouse (10 sources):
abnormal cone electrophysiology,
abnormal rod electrophysiology,
decreased retina cone cell number,
decreased total retina thickness,
nervous system phenotype,
postnatal lethality, complete penetrance,
retina pigment epithelium atrophy,
short photoreceptor inner segment,
short photoreceptor outer segment,
thin retina outer nuclear layer
|
View all ortholog results at Monarch
|
Gene expression phenotype annotations where the gene of interest has been
disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from
differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1,
FDR <= 0.05 and an absolute LogFC >= 2.