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Rabbit Anti-FAM90A1 antibody
Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM90A gene product has been provisionally designated FAM90A pending further characterization.
Similarity:
FAM90A1 belongs to subfamily I of the primate specific FAM90A gene family, which originated from multiple duplications and rearrangements
SWISS:
Q86YD7
Gene ID:
55138
Database links:
Entrez Gene: 55138 Human
Omim: 613041 Human
SwissProt: Q86YD7 Human
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