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Rabbit Anti-C19orf56 antibody
C19orf56 is a 106 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Subcellular Location:
Membrane.
Similarity:
Belongs to the UPF0139 (CGI-140) family.
SWISS:
Q9Y284
Gene ID:
51398
Database links:
Entrez Gene: 51398 Human
SwissProt: Q9Y284 Human
SwissProt: Q6ZWX0 Mouse
Unigene: 108969 Human
Unigene: 657204 Human
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