Monarch Ortholog Phenotypes
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Human (32 sources):
Abnormal electroretinogram,
Abnormality of speech or vocalization,
Brachydactyly,
Cognitive impairment,
Cryptorchidism,
Downslanted palpebral fissures,
External genital hypoplasia,
Finger syndactyly,
Generalized hirsutism,
Hearing impairment,
Hepatic fibrosis,
Hypertension,
Hypogonadism,
Hypoplasia of penis,
Hypoplasia of the ovary,
Intellectual disability,
Low-set, posteriorly rotated ears,
Macular dystrophy,
Medial flaring of the eyebrow,
Multicystic kidney dysplasia,
Nephrotic syndrome,
Nystagmus,
Obesity,
Pigmentary retinopathy,
Polydactyly,
Postaxial hand polydactyly,
Prominent nasal bridge,
Rod-cone dystrophy,
Short neck,
Short stature,
Skeletal muscle atrophy,
Syndactyly
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Mouse (33 sources):
abnormal PR interval,
abnormal adipose tissue amount,
abnormal bone mineralization,
abnormal circulating alanine transaminase level,
abnormal circulating aspartate transaminase level,
abnormal circulating triglyceride level,
abnormal fasting circulating glucose level,
abnormal grip strength,
abnormal heart weight,
abnormal hematocrit,
abnormal hemoglobin content,
abnormal lean body mass,
abnormal mean corpuscular volume,
cardiovascular system phenotype,
decreased bone mineral content,
decreased circulating bilirubin level,
decreased dendritic spine density,
decreased dendritic spine length,
decreased grip strength,
decreased heart rate variability,
decreased heart weight,
decreased lean body mass,
decreased locomotor activity,
decreased respiratory quotient,
decreased spleen weight,
increased anxiety-related response,
increased circulating alanine transaminase level,
increased circulating alkaline phosphatase level,
increased circulating aspartate transaminase level,
increased circulating fructosamine level,
increased circulating glucose level,
increased fasting circulating glucose level,
increased total body fat amount
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View all ortholog results at Monarch
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