Entity Details

Primary name DNSL3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ13609
EntryNameDNSL3_HUMAN
FullNameDeoxyribonuclease gamma
TaxID9606
Evidenceevidence at protein level
Length305
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesDNASE1L3

GO terms

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GOName
GO:0000737 DNA catabolic process, endonucleolytic
GO:0002283 neutrophil activation involved in immune response
GO:0002673 regulation of acute inflammatory response
GO:0003677 DNA binding
GO:0004530 deoxyribonuclease I activity
GO:0004536 deoxyribonuclease activity
GO:0005509 calcium ion binding
GO:0005576 extracellular region
GO:0005634 nucleus
GO:0005783 endoplasmic reticulum
GO:0006259 DNA metabolic process
GO:0006308 DNA catabolic process
GO:0006309 apoptotic DNA fragmentation
GO:0010623 programmed cell death involved in cell development
GO:0070948 regulation of neutrophil mediated cytotoxicity

Subcellular Location

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Subcellular Location
Endoplasmic reticulum
Nucleus
Secreted

Domains

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DomainNameCategoryType
IPR005135 Endonuclease/exonuclease/phosphataseDomainDomain
IPR016202 Deoxyribonuclease IFamilyFamily
IPR018057 Deoxyribonuclease I, active siteSiteActive site
IPR033125 Deoxyribonuclease I, conservied siteSiteConserved site
IPR036691 Endonuclease/exonuclease/phosphatase superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
614420 OMIMSystemic lupus erythematosus 16 (SLEB16)A rare autosomal recessive form of systemic lupus erythematosus with childhood onset, characterized by high frequency of anti-neutrophil cytoplasmic antibodies and lupus nephritis. Systemic lupus erythematosus is a chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. The disease is caused by variants affecting the gene represented in this entry.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
DNSL3_HUMANCRTP1_HUMANBioGRID, IntAct32296183 details
DNSL3_HUMANKRA59_HUMANBioGRID, IntAct32296183 details