| Monarch Ortholog Phenotypes
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Human (44 sources):
Abnormal cornea morphology,
Abnormal respiratory motile cilium morphology,
Abnormality of the digestive system,
Abnormality of the immune system,
Absent frontal sinuses,
Airway obstruction,
Anosmia,
Asplenia,
Asthma,
Atelectasis,
Bronchiectasis,
Chronic bronchitis,
Chronic otitis media,
Chronic rhinitis,
Chronic sinusitis,
Ciliary dyskinesia,
Clubbing of fingers,
Communicating hydrocephalus,
Conductive hearing impairment,
Corneal dystrophy,
Cough,
Delayed speech and language development,
Ectopic pregnancy,
Glue ear,
Halitosis,
Headache,
Hydrocephalus,
Immotile cilia,
Impaired nasal mucociliary clearance,
Infertility,
Male infertility,
Miscarriage,
Nasal polyposis,
Pectus excavatum,
Pneumonia,
Recurrent respiratory infections,
Reduced sperm motility,
Respiratory distress,
Rhinitis,
Scoliosis,
Sinusitis,
Situs inversus totalis,
Tachypnea,
Ventriculomegaly
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Mouse (16 sources):
abdominal situs ambiguus,
abnormal motile cilium morphology,
abnormal motile cilium physiology,
abnormal mucociliary clearance,
abnormal respiratory sounds,
atrioventricular septal defect,
bronchial situs inversus,
coughing,
dual inferior vena cava,
immotile respiratory cilia,
[+]
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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.