Entity Details

Primary name NLRP7
Entity type gene
Source Source Link

Details

PrimaryID199713
RefseqGeneNG_008056
SymbolNLRP7
NameNLR family pyrin domain containing 7
Chromosome19
Location19q13.42
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-04-30
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsNALP7_HUMAN

GO terms

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GOName
GO:0005524 ATP binding
GO:0010955 negative regulation of protein processing
GO:0019828 aspartic-type endopeptidase inhibitor activity
GO:0019966 interleukin-1 binding
GO:0032691 negative regulation of interleukin-1 beta production
GO:0042802 identical protein binding
GO:0071222 cellular response to lipopolysaccharide
GO:0071347 cellular response to interleukin-1
GO:0089720 caspase binding
GO:1900016 negative regulation of cytokine production involved in inflammatory response
GO:1905246 negative regulation of aspartic-type peptidase activity

Diseases

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Disease IDSourceNameDescription
231090 OMIMHydatidiform mole, recurrent, 1 (HYDM1)A disorder characterized by excessive trophoblast development that produces a growing mass of tissue inside the uterus at the beginning of a pregnancy. It leads to abnormal pregnancies with no embryo, and cystic degeneration of the chorionic villi. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
NLRP7NLRP7IntAct25082979 details
NLRP7FAF1BioGRID17046979 details
NLRP7ZBTB16BioGRID26121690 details
NLRP7STAMBPBioGRID28492230 details