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speculate that TTC7 plays an important role in iron transport
Ttc7 is expressed in multiple types of tissue including skin, kidney, spleen, and thymus, but is most abundant in germinal center B cells and hematopoietic stem cells, suggesting an important role in the development of immune system cells
Data confirmed that the Ttc7 mutations, is responsible for abnormal phenotypes observed in various tissues of mice with the flaky skin mutation.
identified a perfectly segregating homozygous missense mutation in TTC7A in a consanguinous Turkish pedigree causing combined immunodeficiency with mild structural intestinal defects
Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
Identify loss of function mutations in TTC7A in 5 infants with very early onset inflammatory bowel disease.
TTC7A deficiency results in increased Rho kinase (show ROCK1 Antibodies) activity, which disrupts polarity, growth, and differentiation of intestinal epithelial cells in multiple intestinal atresia.
These data strongly suggest that TTC7A gene defects cause combined immunodeficiency with multiple intestinal atresias.
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia.
The tetratricopeptide repeat (TPR) domain is defined by a degenerate consensus sequence of 34 amino acids. TPR domain-containing proteins, such as TTC7A, have diverse functions in cell cycle control, protein transport, phosphate turnover, and protein trafficking or secretion, and they can act as chaperones or scaffolding proteins (White et al., 2005
TPR repeat protein 7A
, tetratricopeptide repeat protein 7A
, tetratricopeptide repeat domain 7