| Monarch Ortholog Phenotypes
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Human (33 sources):
Abdominal distention,
Abnormal blistering of the skin,
Abnormality of the genitourinary system,
Anonychia,
Aplasia cutis congenita,
Aplasia of the bladder,
Arthrogryposis multiplex congenita,
Atrophic scars,
Axillary pterygium,
Congenital pyloric atresia,
Ectropion,
Elevated maternal serum alpha-fetoprotein,
Enamel hypoplasia,
Esophageal atresia,
Fragile skin,
Hematuria,
Hydronephrosis,
Intestinal atresia,
Intractable diarrhea,
Milia,
Nail dysplasia,
Nail dystrophy,
Nausea and vomiting,
Oral mucosal blisters,
Polyhydramnios,
Pterygium,
Recurrent skin infections,
Renal duplication,
Renal dysplasia,
Subepidermal blistering with cleavage in the lamina lucida,
Ureterocele,
Urethral stricture,
Urinary bladder inflammation
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Mouse (18 sources):
abnormal Schwann cell physiology,
abnormal axon morphology,
abnormal basement membrane morphology,
abnormal cerebral cortex morphology,
abnormal neuronal precursor cell migration,
abnormal retina nerve fiber layer morphology,
abnormal sciatic nerve morphology,
abnormal skin condition,
abnormal tumor vascularization,
abnormal vitreous body morphology,
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View all ortholog results at Monarch
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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.