重组7号染色体开放阅读框10蛋白
交货期:1周
产品别名:Recombinant SUGCT
Recombinant succinyl-CoA:glutarate-CoA transferase protein
基因名:
SUGCT
产品别名:
C7orf10; DERP13; GA3; ORF19; SUGCT; succinyl-CoA:glutarate-CoA transferase; succinyl-CoA:glutarate-CoA transferase; succinate--hydroxymethylglutarate CoA-transferase; Russel-Silver syndrome candidate; dermal papilla-derived protein 13; succinylCoA:glutarate-CoA transferase; 7号染色体开放阅读框10;
背景信息:
Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf10 gene product has been provisionally designated C7orf10 pending further characterization.
产品发布日期:2026.03.20