人 SMC1A (NM_001281463) cDNA克隆

Accession: NM_001281463
基因名称: SMC1A
基因别名: SMC1; SMCB; CDLS2; SB1.8; SMC1L1; DXS423E; SMC1alpha
基因描述: Homo sapiens structural maintenance of chromosomes 1A (SMC1A), transcript variant 2, mRNA.
种属: Human
CDS区长度: 3636 (查看编码区序列)
翻译后氨基酸长度: 1211 (查看氨基酸序列)
Transcript Variant: This variant (2) differs in the 5' UTR and has multiple coding region differences, compared to variant 1. These differences cause translation initiation at a downstream AUG and result in an isoform (2) with a shorter N-terminus, compared to isoform 1.
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G124756 人 SMC1A (NM_001281463) cDNA克隆 pDONR223 2ug质粒 点击询价

Proper cohesion of sister chromatids is a prerequisite for the correct segregation of chromosomes during cell division. The cohesin multiprotein complex is required for sister chromatid cohesion. This complex is composed partly of two structural maintenance of chromosomes (SMC) proteins, SMC3 and either SMC1B or the protein encoded by this gene. Most of the cohesin complexes dissociate from the chromosomes before mitosis, although those complexes at the kinetochore remain. Therefore, the encoded protein is thought to be an important part of functional kinetochores. In addition, this protein interacts with BRCA1 and is phosphorylated by ATM, indicating a potential role for this protein in DNA repair. This gene, which belongs to the SMC gene family, is located in an area of the X-chromosome that escapes X inactivation. Mutations in this gene result in Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]