Human (47 sources):
Abnormal cardiovascular system morphology,
Abnormal epiphysis morphology,
Abnormal pinna 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,
Highly arched eyebrow,
High palate,
Hyperphalangy of the 2nd finger,
Hypertelorism,
Intrauterine growth retardation,
Joint dislocation,
Joint stiffness,
Low-set ears,
Malar flattening,
Metatarsus valgus,
Micrognathia,
obsolete Joint hyperflexibility,
obsolete Joint laxity,
obsolete Low-set, posteriorly rotated ears,
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
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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.