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5号染色体开放阅读框4抗体
半岛bd体育手机客户端 介绍
靶标:
FAXDC2 半岛bd体育手机客户端 别名: C5orf4; FAXDC2; fatty acid hydroxylase domain containing 2; fatty acid hydroxylase domain containing 2; fatty acid hydroxylase domain-containing protein 2; 5号染色体开放阅读框4; 背景信息:
With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf4 gene product has been provisionally designated C5orf4 pending further characterization.
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