Human (63 sources):
Abnormal cardiac septum morphology,
Abnormal dermatoglyphics,
Abnormal form of the vertebral bodies,
Abnormal localization of kidney,
Abnormality of dental morphology,
Abnormality of immune system physiology,
Abnormality of the dentition,
Blue sclerae,
Butterfly vertebrae,
Cerebral cortical atrophy,
Cleft palate,
Coarctation of aorta,
Coloboma,
Conductive hearing impairment,
Congenital diaphragmatic hernia,
Crossed fused renal ectopia,
Cryptorchidism,
Duplicated collecting system,
EEG abnormality,
Eversion of lateral third of lower eyelids,
Failure to thrive,
Feeding difficulties,
Hemivertebrae,
High palate,
Highly arched eyebrow,
Hip dislocation,
Hydrocephalus,
Hydronephrosis,
Hypodontia,
Hypoplasia of penis,
Hypospadias,
Hypotonia,
Lip pit,
Long eyelashes,
Macrotia,
Mask-like facies,
Microcephaly,
Microcornea,
Microdontia,
Nystagmus,
Obesity,
Orofacial cleft,
Preauricular skin tag,
Precocious puberty,
Protruding ear,
Ptosis,
Recurrent infections,
Renal hypoplasia/aplasia,
Scoliosis,
Seizure,
Sensorineural hearing impairment,
Short 5th finger,
Short columella,
Short middle phalanx of finger,
Short stature,
Small hand,
Sparse lateral eyebrow,
Strabismus,
Ureteropelvic junction obstruction,
Ventriculomegaly,
Vertebral clefting,
Widely spaced teeth,
obsolete Joint hyperflexibility
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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.