KLH conjugated synthetic peptide derived from human C22orf32:41-107/107
Conjugation:
Unconjugated
Alternative Names:
Chromosome 22 open reading frame 32, EMRE_HUMAN, DDDD, dJ186O1.1, mitochondrial, UPF0466 protein C22orf32.
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 C22orf32 gene product has been provisionally designated C22orf32 pending further characterization
