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- accession：NM_001018113
- 基因别名：FANCB
- 基因描述：Homo sapiens Fanconi anemia, complementation group B (FANCB), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：2580
- 翻译后氨基酸长度：859
- TranscriptVariant：This variant (1) represents the longer transcript. Variants 1 and 2 encode the same protein.
- 基因简介：The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group B. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
