Human (58 sources):
Antegonial notching of mandible,
Atrial fibrillation,
Atrioventricular block,
Bidirectional ventricular ectopy,
Blepharophimosis,
Brachydactyly,
Bradycardia,
Broad forehead,
Bulbous nose,
Cleft palate,
Clinodactyly of the 5th finger,
Clinodactyly of the 5th toe,
Delayed eruption of permanent teeth,
Delayed skeletal maturation,
Depression,
Enamel hypoplasia,
Facial asymmetry,
Growth abnormality,
High palate,
Hypertelorism,
Hypokalemia,
Hypoplasia of the maxilla,
Low-set ears,
Malar flattening,
Microcephaly,
Micrognathia,
Oligodontia,
Palpitations,
Paroxysmal atrial fibrillation,
Periodic hypokalemic paresis,
Periodic paralysis,
Persistence of primary teeth,
Preauricular pit,
Prolonged QT interval,
Prominent U wave,
Prominent frontal sinuses,
Scapular winging,
Scoliosis,
Short foot,
Short mandibular rami,
Short metacarpal,
Short metatarsal,
Short palm,
Short palpebral fissure,
Short phalanx of finger,
Shortened QT interval,
Slender long bone,
Small hand,
Specific learning disability,
Sudden cardiac death,
Syncope,
Tachycardia,
Thin upper lip vermilion,
Toe syndactyly,
Triangular face,
Ventricular arrhythmia,
Ventricular fibrillation,
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.