| Monarch Ortholog Phenotypes
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Human (7 sources):
Abnormality of dental morphology,
Abnormality of the face,
Cough,
Hypoplasia of the maxilla,
Microdontia,
Micrognathia,
Oligodontia
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Mouse (29 sources):
Meibomian gland hypoplasia,
abnormal adipose tissue distribution,
abnormal coat appearance,
abnormal corneal stroma development,
abnormal eyelid development,
abnormal hair follicle development,
abnormal hair follicle morphology,
abnormal hair follicle orientation,
abnormal hair medulla,
abnormal vibrissa morphology,
abnormal zigzag hair morphology,
absent Descemet membrane,
absent eye anterior chamber,
cardiovascular system phenotype,
curly vibrissae,
decreased body size,
decreased guard hair length,
disheveled coat,
eyelid hyperplasia,
eyelids open at birth,
failure of eyelid fusion,
immune system phenotype,
increased corneal stroma thickness,
increased curvature of hairs,
increased incidence of corneal inflammation,
kinked vibrissae,
orbicularis oculi muscle hypoplasia,
ruptured lens capsule,
wavy vibrissae
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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.