Human (62 sources):
2-3 toe syndactyly,
Abnormal cardiovascular system morphology,
Abnormal chorioretinal morphology,
Accessory spleen,
Ambiguous genitalia,
Anencephaly,
Anophthalmia,
Aplasia/Hypoplasia of the corpus callosum,
Aplasia/Hypoplasia of the iris,
Aplasia/Hypoplasia of the tongue,
Arthrogryposis multiplex congenita,
Asplenia,
Bowing of the long bones,
Cataract,
Cerebellar hypoplasia,
Cleft palate,
Clinodactyly of the 5th finger,
Congenital hepatic fibrosis,
Cryptorchidism,
Cystic hygroma,
Cystic liver disease,
Dandy-Walker malformation,
Depressed nasal ridge,
Encephalocele,
Full cheeks,
Furrowed tongue,
Hydranencephaly,
Hydrocephalus,
Hypertelorism,
Hypoplasia of the brainstem,
Lobar holoprosencephaly,
Low-set, posteriorly rotated ears,
Male pseudohermaphroditism,
Microcephaly,
Microcornea,
Micrognathia,
Microphthalmia,
Microretrognathia,
Multicystic kidney dysplasia,
Narrow nasal ridge,
Oligohydramnios,
Optic atrophy,
Pancreatic cysts,
Pancreatic fibrosis,
Postaxial foot polydactyly,
Postaxial hand polydactyly,
Potter facies,
Preaxial hand polydactyly,
Pulmonary hypoplasia,
Redundant neck skin,
Renal agenesis,
Renal cyst,
Renal dysplasia,
Renal hypoplasia,
Sclerocornea,
Single transverse palmar crease,
Situs inversus totalis,
Sloping forehead,
Talipes equinovarus,
True hermaphroditism,
Ureteral duplication,
Urethral atresia
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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.