人 CHRND (NM_001256657) cDNA克隆

Accession: NM_001256657
基因名称: CHRND
基因别名: ACHRD; CMS2A; FCCMS; SCCMS
基因描述: Homo sapiens cholinergic receptor, nicotinic, delta (muscle) (CHRND), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1509 (查看编码区序列)
翻译后氨基酸长度: 502 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks an alternate in-frame exon compared to variant 1. The resulting isoform (2) has the same N- and C-termini but is shorter compared to isoform 1.
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G128077 人 CHRND (NM_001256657) cDNA克隆 pDONR223 2ug质粒 点击询价

The acetylcholine receptor of muscle has 5 subunits of 4 different types: 2 alpha and 1 each of beta, gamma and delta subunits. After acetylcholine binding, the receptor undergoes an extensive conformation change that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Defects in this gene are a cause of multiple pterygium syndrome lethal type (MUPSL), congenital myasthenic syndrome slow-channel type (SCCMS), and congenital myasthenic syndrome fast-channel type (FCCMS). Several transcript variants, some protein-coding and some not, have been found for this gene. [provided by RefSeq, Feb 2012]