Description
Product Characteristics:
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 C7orf44 gene product has been provisionally designated C7orf44 pending further characterization.
Subcellular location: Cytoplasm
Synonyms: Chromosome 7 open reading frame 44, FLJ10803, Hypothetical protein LOC55744, Uncharacterized protein C7orf44,COA1_HUMAN.
Target Information: Please see product details or send an inquiry to antibodies-online for additional target information