人 OBSCN (NM_001271223) cDNA克隆

Accession: NM_001271223
基因名称: OBSCN
基因别名: UNC89; ARHGEF30
基因描述: Homo sapiens obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF (OBSCN), transcript variant IC, mRNA.
种属: Human
CDS区长度: 26772 (查看编码区序列)
翻译后氨基酸长度: 8923 (查看氨基酸序列)
Transcript Variant: This variant (IC) represents an inferred complete model that includes additional in-frame coding exons with consensus splice sites. The exons included in this inferred variant are supported by a combination of available cDNA data and sequence analysis of repetitive exons. This transcript represents a predicted protein (isoform IC) of 8,923 amino acids.
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G121844 人 OBSCN (NM_001271223) cDNA克隆 pDONR223 2ug质粒 点击询价

The obscurin gene spans more than 150 kb, contains over 80 exons and encodes a protein of approximately 720 kDa. The encoded protein contains 68 Ig domains, 2 fibronectin domains, 1 calcium/calmodulin-binding domain, 1 RhoGEF domain with an associated PH domain, and 2 serine-threonine kinase domains. This protein belongs to the family of giant sacromeric signaling proteins that includes titin and nebulin, and may have a role in the organization of myofibrils during assembly and may mediate interactions between the sarcoplasmic reticulum and myofibrils. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]