Human (76 sources):
Abnormal electroretinogram,
Abnormal retinal vascular morphology,
Abnormal testis morphology,
Abnormality of fundus pigmentation,
Abnormality of metabolism/homeostasis,
Abnormality of retinal pigmentation,
Abnormality of the digestive system,
Abnormality of the immune system,
Airway obstruction,
Anteverted nares,
Asplenia,
Asthma,
Atelectasis,
Atypical scarring of skin,
Blindness,
Bronchiectasis,
Cataract,
Chronic bronchitis,
Chronic otitis media,
Chronic sinusitis,
Clubbing of fingers,
Color vision defect,
Conductive hearing impairment,
Cone/cone-rod dystrophy,
Congenital stationary cone dysfunction,
Constriction of peripheral visual field,
Corneal dystrophy,
Cough,
Delayed speech and language development,
Ectopic pregnancy,
Glaucoma,
Glue ear,
Halitosis,
Headache,
High-frequency hearing impairment,
Hydrocephalus,
Hyperinsulinemia,
Hyperreflexia,
Hypogonadism,
Hypoplasia of penis,
Immotile cilia,
Impaired nasal mucociliary clearance,
Infertility,
Intellectual disability,
Keratoconus,
Macular degeneration,
Macular scar,
Miscarriage,
Myopia,
Nasal polyposis,
Nyctalopia,
Nystagmus,
Obesity,
Ophthalmoplegia,
Optic atrophy,
Otitis media,
Pectus excavatum,
Photophobia,
Pneumonia,
Progressive night blindness,
Recurrent Haemophilus influenzae infections,
Recurrent bronchitis,
Recurrent respiratory infections,
Reduced sperm motility,
Reduced visual acuity,
Respiratory distress,
Rhinitis,
Rod-cone dystrophy,
Scoliosis,
Sensorineural hearing impairment,
Situs inversus totalis,
Tachypnea,
Type II diabetes mellitus,
Ventriculomegaly,
Visual impairment,
Wide nasal bridge
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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.