| Monarch Ortholog Phenotypes
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Human (38 sources):
Abnormality of body height,
Abnormality of the dentition,
Abnormality of the voice,
Absence of pubertal development,
Absence of secondary sex characteristics,
Anxiety,
Azoospermia,
Breast hypoplasia,
Camptodactyly,
Cleft palate,
Congenital sensorineural hearing impairment,
Cryptorchidism,
Decreased serum testosterone concentration,
Decreased testicular size,
Delayed puberty,
Delayed skeletal maturation,
Depressed nasal bridge,
Depression,
Eunuchoid habitus,
Female hypogonadism,
Generalized joint hypermobility,
Gynecomastia,
Hypertelorism,
Hypogonadotropic hypogonadism,
Hypoplasia of the ovary,
Hypoplasia of the uterus,
Impotence,
Increased female libido,
Male hypogonadism,
Micropenis,
Non-obstructive azoospermia,
Osteopenia,
Osteoporosis,
Phenotypic abnormality,
Primary amenorrhea,
Secondary amenorrhea,
Sparse body hair,
Wide intermamillary distance
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Mouse (32 sources):
abnormal anogenital distance,
abnormal female reproductive system morphology,
abnormal gametogenesis,
abnormal hormone level,
abnormal pituitary gland physiology,
abnormal sex gland morphology,
abnormal splenic cell ratio,
abnormal vagina orifice morphology,
absent Leydig cells,
arrest of male meiosis,
decreased adrenocorticotropin level,
decreased follicle stimulating hormone level,
decreased luteinizing hormone level,
decreased prolactin level,
delayed female fertility,
delayed vaginal opening,
impaired ovarian folliculogenesis,
increased bone marrow cell number,
increased circulating estradiol level,
increased circulating progesterone level,
increased immature B cell number,
increased mature B cell number,
nervous system phenotype,
short diestrus,
short estrous cycle,
short metestrus,
short proestrus,
skeleton phenotype,
small ovary,
small penis,
small seminal vesicle,
small uterus
[+]
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View all ortholog results at Monarch
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These phenotypes are associated with this gene with a has phenotype relation via Monarch.