| Monarch Ortholog Phenotypes
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Human (34 sources):
Abnormal hip joint morphology,
Abnormality of epiphysis morphology,
Amblyopia,
Arthralgia,
Astigmatism,
Cataract,
Cleft palate,
Delayed epiphyseal ossification,
Elevated circulating creatine kinase concentration,
Epiphyseal dysplasia,
Flat face,
Gait disturbance,
Genu valgum,
Genu varum,
Hip dysplasia,
Irregular epiphyses,
Irregular vertebral endplates,
Limitation of joint mobility,
Malar flattening,
Micrognathia,
Micromelia,
Mild short stature,
Mildly elevated creatine kinase,
Myopia,
Osteoarthritis,
Platyspondyly,
Proximal muscle weakness,
Retinal detachment,
Sensorineural hearing impairment,
Short metacarpal,
Short stature,
Small epiphyses,
Vitreoretinopathy,
obsolete Joint hyperflexibility
[+]
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Mouse (4 sources):
abnormal seminal vesicle morphology,
decreased body length,
enlarged lymph nodes,
prolonged RR interval
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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.