| Monarch Ortholog Phenotypes
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Human (32 sources):
Abnormal erythrocyte morphology,
Agenesis of corpus callosum,
Anal atresia,
Aplasia cutis congenita,
Atopic dermatitis,
Atrial septal defect,
Bifid nasal tip,
Brachycephaly,
Coronal cleft vertebrae,
Depressed nasal ridge,
Dysplasia of the femoral head,
Dysplastic corpus callosum,
Epiphyseal dysplasia,
Global developmental delay,
High palate,
Highly arched eyebrow,
Hypodontia,
Microtia,
Midface retrusion,
Oligohydramnios,
Patent foramen ovale,
Recurrent urinary tract infections,
Refractory anemia with ringed sideroblasts,
Renal hypoplasia,
Severe short stature,
Short neck,
Short nose,
Sideroblastic anemia,
Sparse hair,
Synophrys,
Vertebral clefting,
Vesicoureteral reflux
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Mouse (3 sources):
decreased pre-B cell number,
embryonic lethality, complete penetrance,
hematopoietic system phenotype
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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.