Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The FAM83F gene product has been provisionally designated FAM83F pending further characterization.
Similarity:
Belongs to the FAM83 family.
SWISS:
Q8NEG4
Gene ID:
22828
Database links:
Entrez Gene: 22828 Human
Entrez Gene: 213956 Mouse
SwissProt: Q8NEG4 Human
SwissProt: Q3UKU4 Mouse
Unigene: 197136 Human
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Sample: Small intestine (Mouse) Lysate at 40 ug
Primary: Anti-FAM83F (SL11009R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 55 kD
Observed band size: 55 kD
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