| Monarch Ortholog Phenotypes
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Human (22 sources):
Abnormality of the musculature,
Arthrogryposis multiplex congenita,
Cardiac myxoma,
Cutaneous syndactyly of toes,
Deep philtrum,
Distal arthrogryposis,
Dysphagia,
Facial asymmetry,
Feeding difficulties,
Hammertoe,
Hip dislocation,
Limitation of joint mobility,
Macrocephaly,
Mandibular prognathia,
Metatarsus adductus,
Micrognathia,
Ptosis,
Short stature,
Symphalangism affecting the phalanges of the hand,
Talipes equinovarus,
Tall chin,
Trismus
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Mouse (3 sources):
abnormal craniofacial morphology,
abnormal embryo size,
preweaning lethality, complete penetrance
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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.