Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. 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. FAM86A and FAM86B2 are 330 amino acid proteins that belongs to the FAM86 family. The gene encoding FAM86A maps to human chromosome 16 whereas the gene encoding FAM86B2 maps to human chromosome 8.
Subunit:
Interacts with FAM86B2 and FAM86C1.
Subcellular Location:
Cytoplasm.
Similarity:
Belongs to the FAM86 family.
SWISS:
Q96G04
Gene ID:
196483
Database links:
Entrez Gene: 196483 Human
SwissProt: Q96G04 Human
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