人 NLRP3 (NM_183395) cDNA克隆

Accession: NM_183395
基因名称: NLRP3
基因别名: AII; AVP; FCU; MWS; FCAS; CIAS1; NALP3; C1orf7; CLR1.1; PYPAF1; AGTAVPRL
基因描述: Homo sapiens NLR family, pyrin domain containing 3 (NLRP3), transcript variant 2, mRNA.
种属: Human
CDS区长度: 2769 (查看编码区序列)
翻译后氨基酸长度: 922 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks two alternate in-frame exons, which are located in the mid-coding and 3' coding regions, compared to variant 1. The encoded isoform (b) is shorter than isoform a.
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G122489 人 NLRP3 (NM_183395) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a pyrin-like protein containing a pyrin domain, a nucleotide-binding site (NBS) domain, and a leucine-rich repeat (LRR) motif. This protein interacts with the apoptosis-associated speck-like protein PYCARD/ASC, which contains a caspase recruitment domain, and is a member of the NALP3 inflammasome complex. This complex functions as an upstream activator of NF-kappaB signaling, and it plays a role in the regulation of inflammation, the immune response, and apoptosis. Mutations in this gene are associated with familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), chronic infantile neurological cutaneous and articular (CINCA) syndrome, and neonatal-onset multisystem inflammatory disease (NOMID). Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. Alternative 5' UTR structures are suggested by available data; however, insufficient evidence is available to determine if all of the represented 5' UTR splice patterns are biologically valid. [provided by RefSeq, Oct 2008]