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Antibody detects endogenous levels of total FAM96B.
Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The FAM96B gene product has been provisionally designated FAM96B pending further characterization.
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Protein Aliases: Cytosolic iron-sulfur assembly component 2B; family with sequence similarity 96, member B; Mitotic spindle-associated MMXD complex subunit MIP18; MSS19-interacting protein of 18 kDa; Protein FAM96B
Gene Aliases: 1110019N10Rik; CGI-128; CIAB; CIAO2B; FAM96B; HSPC118; MIP18; RGD1311762
UniProt ID: (Human) Q9Y3D0, (Mouse) Q9D187
Entrez Gene ID: (Human) 51647, (Mouse) 68523, (Rat) 680987
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