Home
>
Product
>
Antibody
>
Rabbit Anti-C22orf32 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 C22orf32 gene product has been provisionally designated C22orf32 pending further characterization
Subcellular Location:
Mitochondrion (Potential). Membrane; Single-pass membrane protein (Potential).
Similarity:
Belongs to the UPF0466 family.
SWISS:
Q9H4I9
Gene ID:
91689
Database links:
Entrez Gene: 91689 Human
SwissProt: Q9H4I9 Human
Unigene: 306083 Human
|
|