人 FANCC (NM_001243743) cDNA克隆

基本信息

Accession: NM_001243743
基因名称: FANCC
基因别名: FA3; FAC; FACC
基因描述: Homo sapiens Fanconi anemia, complementation group C (FANCC), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1677 (查看编码区序列)
翻译后氨基酸长度: 558 (查看氨基酸序列)
Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Both variants 1 and 2 encode the same isoform (a).

订购信息

产品编号 产品名称 载体 规格 价格
G112265 人 FANCC (NM_001243743) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 FANCC (NM_000136) cDNA克隆 transcript variant 1
人 FANCC (NM_001243743) cDNA克隆 transcript variant 2
人 FANCC (NM_001243744) cDNA克隆 transcript variant 3

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 C. [provided by RefSeq, Jul 2008]

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