| Monarch Ortholog Phenotypes
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Human (29 sources):
Abnormality of epiphysis morphology,
Amblyopia,
Arthralgia,
Astigmatism,
Cataract,
Cleft palate,
Degenerative vitreoretinopathy,
Epiphyseal dysplasia,
Flat capital femoral epiphysis,
Flat face,
Gait disturbance,
Genu valgum,
Genu varum,
High myopia,
Hip dysplasia,
Irregular capital femoral epiphysis,
Irregular vertebral endplates,
Limitation of joint mobility,
Malar flattening,
Micrognathia,
Micromelia,
Myopia,
Osteoarthritis,
Platyspondyly,
Retinal detachment,
Sensorineural hearing impairment,
Short stature,
Vitreoretinopathy,
obsolete Joint hyperflexibility
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Mouse (11 sources):
abnormal articular cartilage morphology,
abnormal bone healing,
abnormal knee joint morphology,
abnormal patella morphology,
abnormal tectorial membrane morphology,
abnormal tectorial membrane striated-sheet matrix morphology,
absent cartilage,
enlarged tectorial membrane,
increased chondrocyte proliferation,
increased or absent threshold for auditory brainstem response,
[+]
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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.