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Rabbit Anti-FAM188B antibody
FAM188B is a 757 amino acid protein this is encoded by a gene that maps to human chromosome 7. Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. 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.
Similarity:
Belongs to the FAM188 family.
SWISS:
Q4G0A6
Gene ID:
84182
Database links:
Entrez Gene: 84182 Human
SwissProt: Q4G0A6 Human
Unigene: 660192 Human
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