Human (65 sources):
Abdominal distention,
Abnormal digit morphology,
Abnormal prolactin level,
Abnormality of secondary sexual hair,
Abnormality of the face,
Abnormality of the hypothalamus-pituitary axis,
Abnormality of the orbital region,
Absence of secondary sex characteristics,
Absent septum pellucidum,
Adrenal hypoplasia,
Adrenal insufficiency,
Agenesis of corpus callosum,
Amenorrhea,
Anterior pituitary agenesis,
Anterior pituitary hypoplasia,
Aplasia/Hypoplasia of the breasts,
Central hypothyroidism,
Coarse facial features,
Constipation,
Cryptorchidism,
Decreased cervical spine mobility,
Decreased circulating ACTH level,
Decreased response to growth hormone stimulation test,
Decreased testicular size,
Delayed puberty,
Delayed skeletal maturation,
Depressed nasal ridge,
Diabetes insipidus,
Ectopic anterior pituitary gland,
Ectopic posterior pituitary,
Failure to thrive,
Fatigue,
Feeding difficulties,
Global developmental delay,
Growth delay,
Holoprosencephaly,
Hypoglycemia,
Hypogonadotropic hypogonadism,
Hypopituitarism,
Hypoplasia of penis,
Hypotension,
Hypothyroidism,
Hypotonia,
Infertility,
Intellectual disability,
Jaundice,
Large fontanelles,
Marked delay in bone age,
Median cleft lip and palate,
Optic nerve hypoplasia,
Orofacial cleft,
Osteopenia,
Osteoporosis of vertebrae,
Pituitary dwarfism,
Pituitary hypothyroidism,
Polydactyly,
Primary amenorrhea,
Seizure,
Septo-optic dysplasia,
Severe global developmental delay,
Severe postnatal growth retardation,
Short stature,
Sleep disturbance,
Small sella turcica,
Umbilical hernia
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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.