- accession:NM_001127462
- 基因别名:NLRP3
- 基因描述:Homo sapiens NLR family, pyrin domain containing 3 (NLRP3), transcript variant 5, mRNA.
- 载体: 现货载体
- CDS区长度:2940
- 翻译后氨基酸长度:979
- TranscriptVariant:This variant (5) lacks an alternate in-frame exon in the mid-coding region, compared to variant 1. The encoded isoform (d) is shorter than isoform a.
- 基因简介: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]
- 载体信息:自有图片地址
- 规格:10ul 质粒
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