rs62143197
This is a intron variant variant in the NLRP12 gene.
▶GWAS Catalog Trait Associations (101)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (101)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
cold-inducible RNA-binding protein measurement
eukaryotic translation initiation factor 3 subunit G measurement
40S ribosomal protein S3a measurement
eukaryotic translation initiation factor 1A, X-chromosomal measurement
uncharacterized protein KIAA0040 measurement
heterogeneous nuclear ribonucleoprotein A/B amount
dual specificity mitogen-activated protein kinase kinase 1 measurement
protein kinase c beta type (splice variant beta-II) measurement
ribosomal protein S6 kinase alpha-6 measurement
peptidyl-prolyl cis-trans isomerase H measurement
About NLRP12
This gene encodes a member of the CATERPILLER family of cytoplasmic proteins. The encoded protein, which contains an N-terminal pyrin domain, a NACHT domain, a NACHT-associated domain, and a C-terminus leucine-rich repeat region, functions as an attenuating factor of inflammation by suppressing inflammatory responses in activated monocytes. Mutations in this gene cause familial cold autoinflammatory syndrome type 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]
View all NLRP12 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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