| Monarch Ortholog Phenotypes
|
Human (39 sources):
Abnormality of the outer ear,
Anteverted nares,
Arachnodactyly,
Atrial septal defect,
Brachycephaly,
Clinodactyly,
Craniosynostosis,
Cryptorchidism,
Dental malocclusion,
Developmental regression,
Down-sloping shoulders,
Dysphagia,
High myopia,
High palate,
Hip dysplasia,
Hypertelorism,
Hypochromic anemia,
Hypodontia,
Hypoparathyroidism,
Long philtrum,
Long toe,
Low posterior hairline,
Low-set ears,
Microcytic anemia,
Micrognathia,
Mitral regurgitation,
Moderate global developmental delay,
Osteopenia,
Pectus excavatum,
Preauricular skin tag,
Sensorineural hearing impairment,
Short 2nd finger,
Smooth philtrum,
Sparse lateral eyebrow,
Syndactyly,
Tapered finger,
Webbed neck,
Wide mouth,
Wide nasal bridge
[+]
|
|
Mouse (2 sources):
abnormal retina cone bipolar cell morphology,
decreased body size
|
View all ortholog results at Monarch
|
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.