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Proteintech
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Immunogen sequence: MVGGGGVGG GLLENANPLI YQRSGERPVT AGEEDEQVPD SIDAREIFDL IRSINDPEHP LTLEELNVVE QVRVQVSDPE STVAVAFTPT IPHCSMATLI GLSIKVKLLR SLPQRFKMDV HITPGTHASE HAVNKQLADK ERVAAALENT HLLEVVNQCL SARS (1-163 aa encoded by BC001733)
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: CGI-128; CIAB; CIAO2B; FAM96B; HSPC118; MIP18
UniProt ID: (Human) Q9Y3D0
Entrez Gene ID: (Human) 51647
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