基因名：
BABAM1
产品别名：
C19orf62； HSPC142； MERIT40； NBA1； BABAM1； BRISC and BRCA1 A complex member 1； BRISC and BRCA1 A complex member 1； BRISC and BRCA1-A complex member 1； BRCA1-A complex subunit MERIT40； mediator of RAP80 interactions and targeting subunit of 40 kDa； mediator of Rap80 interactions and targeting 40 kDa； new component of the BRCA1-A complex； new component of the BRCAA1 A complex； 乳腺癌易感基因复合物HSPC142；
背景信息：
Consisting of around 63 million bases with over 1,400 genes, chromosome 19 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 Fc?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. The C19orf62 gene product has been provisionally designated C19orf62 pending further characterization.
