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Rabbit Anti-KIAA1671 antibody
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 KIAA1671 gene product has been provisionally designated KIAA1671 pending further characterization.
SWISS:
Q9BY89
Gene ID:
85379
Database links:
Entrez Gene: 85379 Human
SwissProt: Q9BY89 Human
Unigene: 419171 Human
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