ttc7a Phenotypes

Phenotypes

XB-GENEPAGE-949569

Gene Symbol: ttc7a Gene Name: tetratricopeptide repeat domain 7A

Expression Phenotypes 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.
Computed annotations: ttc7a assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (38 sources): Abdominal distention, Abnormal abdomen morphology, Abnormality of the ductus choledochus, Abnormality of the skeletal system, Absent eyebrow, Alopecia of scalp, Autoimmune hemolytic anemia, Autoimmunity, Bloody diarrhea, Congenital pulmonary airway malformation, Duodenal stenosis, Ectopic calcification, Enamel hypoplasia, Gastrointestinal atresia, Hashimoto thyroiditis, Hematochezia, Hepatitis, Hypertelorism, Hypoplasia of the thymus, Immunodeficiency, Interface hepatitis, Intestinal atresia, Intestinal malrotation, Intrauterine growth retardation, Jejunoileal ulceration, Nail dystrophy, Omphalocele, Peritoneal abscess, Polyhydramnios, Prominent forehead, Psoriasiform dermatitis, Rectal abscess, Recurrent abscess formation, Severe combined immunodeficiency, Sparse hair, Thickened skin, Type I diabetes mellitus, Ventricular septal defect [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Human (38 sources): Abdominal distention, Abnormal abdomen morphology, Abnormality of the ductus choledochus, Abnormality of the skeletal system, Absent eyebrow, Alopecia of scalp, Autoimmune hemolytic anemia, Autoimmunity, Bloody diarrhea, Congenital pulmonary airway malformation, [+]