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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
人类
NLRP3 - NLR Family Pyrin Domain Containing 3
Alias:
AII
AVP
FCU
MWS
FCAS
KEFH
CIAS1
FCAS1
NALP3
C1orf7
CLR1.1
DFNA34
PYPAF1
AGTAVPRL
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码一个含有pyrin结构域、核苷酸结合位点(NBS)结构域和亮氨酸富集重复(LRR)基序的pyrin样蛋白。这个蛋白与凋亡相关斑点样蛋白PYCARD/ASC相互作用,PYCARD/ASC含有caspase招募结构域,是NLRP3炎性体复合物的成员。这个复合物作为NF-kappaB信号传导的上游激活子,在炎症、免疫应答和凋亡的调节中发挥作用。SARS-CoV 3a蛋白,一种跨膜孔形成病毒孔蛋白,已被证明通过在巨噬细胞中形成离子通道来激活NLRP3炎性体。这个基因的突变与家族性冷自身炎症综合征(FCAS)、Muckle-Wells综合征(MWS)、慢性婴儿神经皮肤关节(CINCA)综合征、新生儿多系统炎症性疾病(NOMID)、家族性视网膜血管炎、家族性突发性耳聋以及炎症相关的常染色体显性34耳聋有关。这个基因的多种可变剪接转录变异体已被鉴定,编码不同的异构体。现有数据提示存在替代性的5'UTR结构;然而,缺乏足够证据来确定所有表示的5'UTR剪接模式是否都是生物学上有效的。[由RefSeq,2020年8月提供]
Related ID:
NCBI:114548
ENSEMBL:ENSG00000162711
HGNC:16400
UNIPROT:Q96P20
OMIM:606416
Basic Information
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114548
20
10
32741 bp
118.17
830
7
38
75
NLRP3 Genetics information (+)
GRCh38
Sequence Homology
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* This data comes from NCBI.
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