skic2 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (134)

Interactants (0)

XB-GENEPAGE-486232

Gene Symbol: skic2 Gene Name: SKI2 subunit of superkiller complex

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (58 sources): Abnormal facial shape, Abnormal heart morphology, Abnormality of iron homeostasis, Abnormality of skin morphology, Abnormality of the liver, Aortic regurgitation, Atrial septal defect, Bicuspid aortic valve, Bloody diarrhea, Brittle hair, Broad forehead, Cafe-au-lait spot, Cirrhosis, Colitis, Decreased circulating iron concentration, Dependency on intravenous nutrition, Diarrhea, Dry skin, Failure to thrive, Gastritis, Generalized hypopigmentation, Glaucoma, Global developmental delay, Hepatic fibrosis, Hepatitis, Hepatoblastoma, Hepatomegaly, Hypertelorism, Hypopigmentation of hair, Hypoplasia of the thymus, Hypothyroidism, Immunodeficiency, Increased mean platelet volume, Intellectual disability, mild, Intractable diarrhea, Intrauterine growth retardation, Lymphopenia, Panhypogammaglobulinemia, Patent ductus arteriosus, Peripheral pulmonary artery stenosis, Pili canaliculi, Polycystic kidney dysplasia, Prominent forehead, Recurrent infections, Renal hypoplasia, Short stature, Small for gestational age, Sparse hair, Splenomegaly, Tetralogy of Fallot, Thrombocytosis, Trichorrhexis nodosa, Uncombable hair, Ventricular septal defect, Villous atrophy, Wide nasal bridge, Wide nose, Woolly hair [+]
Mouse (4 sources): abnormal embryo size, embryonic lethality between implantation and placentation, complete penetrance, embryonic lethality prior to organogenesis, preweaning lethality, complete penetrance
View all ortholog results at Monarch