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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. Transloacations 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 C22orf13 gene product has been provisionally designated C22orf13 pending further characterization.
Organism species: Homo sapiens (Human)
| CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
| Proteins | n/a | Recombinant Guanylyl Cyclase Domain Containing Protein 1 (GUCD1) | Recombinant Protein Customized Service Offer |
| Antibodies | n/a | Monoclonal Antibody to Guanylyl Cyclase Domain Containing Protein 1 (GUCD1) | Monoclonal Antibody Customized Service Offer |
| n/a | Polyclonal Antibody to Guanylyl Cyclase Domain Containing Protein 1 (GUCD1) | Polyclonal Antibody Customized Service Offer | |
| Assay Kits | n/a | CLIA Kit for Guanylyl Cyclase Domain Containing Protein 1 (GUCD1) | CLIA Kit Customized Service Offer |
| n/a | ELISA Kit for Guanylyl Cyclase Domain Containing Protein 1 (GUCD1) | ELISA Kit Customized Service Offer |
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- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]