Human (47 sources):
Abnormal cardiovascular system morphology,
Abnormal pinna morphology,
Abnormality of epiphysis morphology,
Atrial septal defect,
Camptodactyly,
Camptodactyly of finger,
Chronic otitis media,
Cleft palate,
Cleft upper lip,
Clinodactyly of the 5th finger,
Coarctation of aorta,
Cryptorchidism,
Cystic hygroma,
Dextrocardia,
Failure to thrive,
Full cheeks,
Global developmental delay,
Glossoptosis,
High palate,
Highly arched eyebrow,
Hyperphalangy of the 2nd finger,
Hypertelorism,
Intrauterine growth retardation,
Joint dislocation,
Joint stiffness,
Low-set ears,
Low-set, posteriorly rotated ears,
Malar flattening,
Metatarsus valgus,
Micrognathia,
Oral synechia,
Overriding aorta,
Pectus carinatum,
Pectus excavatum,
Radial deviation of the 2nd finger,
Scoliosis,
Seizure,
Short neck,
Short stature,
Single transverse palmar crease,
Talipes equinovarus,
Ulnar deviation of the 2nd finger,
Umbilical hernia,
Ventricular septal defect,
Ventriculomegaly,
obsolete Joint hyperflexibility,
obsolete Joint laxity
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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.