DNASE2, deoxyribonuclease 2, lysosomal, 1777

N. diseases: 29; N. variants: 6
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.230 Biomarker disease MGD
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.010 GeneticVariation group BEFREE DNase II polymorphisms associated with risk of renal disorder among systemic lupus erythematosus patients. 15723160 2005
CUI: C0002871
Disease: Anemia
Anemia
0.020 Biomarker disease BEFREE DNase II(-/-) embryos suffer from lethal anemia due to IFN-beta produced in the macrophages carrying undigested DNA. 20706988 2010
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.010 AlteredExpression disease BEFREE Based on these results, we can conclude that in the liver of hypothyroid rats the transcriptional activation by T2 of DNL genes could depend, at least in part, on SREBP-1- and ChREBP-dependent mechanisms.© 2019 IUBMB Life, 2019. 30707786 2019
CUI: C0003865
Disease: Arthritis, Adjuvant-Induced
Arthritis, Adjuvant-Induced
0.200 Biomarker disease CTD_mouse Cytokine-dependent but acquired immunity-independent arthritis caused by DNA escaped from degradation. 20974942 2010
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
0.200 Biomarker phenotype CTD_mouse Cytokine-dependent but acquired immunity-independent arthritis caused by DNA escaped from degradation. 20974942 2010
CUI: C0971858
Disease: Arthritis, Collagen-Induced
Arthritis, Collagen-Induced
0.200 Biomarker disease CTD_mouse Cytokine-dependent but acquired immunity-independent arthritis caused by DNA escaped from degradation. 20974942 2010
CUI: C0993582
Disease: Arthritis, Experimental
Arthritis, Experimental
0.200 Biomarker disease CTD_mouse Cytokine-dependent but acquired immunity-independent arthritis caused by DNA escaped from degradation. 20974942 2010
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
0.320 GeneticVariation disease BEFREE Dnase2<sup>-/-</sup> Ifnar<sup>-/-</sup> mice were shown to recapitulate many features of the DNase II-deficient patients including cytopenia, extramedullary hematopoiesis and liver fibrosis. 31464028 2020
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.330 Biomarker disease BEFREE Genetic associations of DNase II with SLE and related phenotypes were examined in Korean patients with SLE. 15723160 2005
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
0.020 Biomarker disease BEFREE Here, we give an overview of the mechanisms of THs action on liver fatty acid metabolism, focusing on the different effects exerted by T2 and T3 on the regulation of the DNL. 28362337 2017
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 GeneticVariation disease BEFREE However, the effects of SNPs in DNL genes on overall survival of HCC patients receiving transarterial chemoembolization (TACE) treatment are still unknown. 25735330 2015
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.030 Biomarker group BEFREE In addition, if nucleases, such as DNase II or DNase III (Trex1), fail to clear self-DNA, accumulated DNA gains access to intracellular compartments where it drives inflammatory responses leading to autoimmune disease. 23417527 2013
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
0.320 AlteredExpression disease BEFREE In fatty livers, DNase II activity is suppressed in contrast to simple inactivation of Bcl-xL or Mcl-1, and both apoptotic and non-apoptotic hepatocyte death can develop, leading to the progression of liver fibrosis. 29855540 2019
CUI: C2895206
Disease: Autoimmune disease (systemic) NOS
Autoimmune disease (systemic) NOS
0.010 Biomarker disease BEFREE Inefficient and abnormal clearance of apoptotic cells (efferocytosis) contributes to systemic autoimmune disease in humans and mice, and inefficient chromosomal DNA degradation by DNAse II leads to systemic polyarthritis and a cytokine storm. 29118755 2017
CUI: C0162323
Disease: Polyarthritis
Polyarthritis
0.010 Biomarker disease BEFREE Inefficient and abnormal clearance of apoptotic cells (efferocytosis) contributes to systemic autoimmune disease in humans and mice, and inefficient chromosomal DNA degradation by DNAse II leads to systemic polyarthritis and a cytokine storm. 29118755 2017
CUI: C0919747
Disease: Cytokine storm
Cytokine storm
0.010 Biomarker disease BEFREE Inefficient and abnormal clearance of apoptotic cells (efferocytosis) contributes to systemic autoimmune disease in humans and mice, and inefficient chromosomal DNA degradation by DNAse II leads to systemic polyarthritis and a cytokine storm. 29118755 2017
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
0.020 Biomarker disease BEFREE Inhibition of DNL is a successful approach to reverse hepatic steatosis, as shown by different studies in mice and humans. 30630736 2019
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis
0.010 Biomarker disease BEFREE Inhibition of DNL is a successful approach to reverse hepatic steatosis, as shown by different studies in mice and humans. 30630736 2019
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.230 GeneticVariation disease BEFREE Intriguingly, homozygosity for the RA associated DNASE2 -1066 G allele had an additive effect on the disease susceptibility conferred by the wt allele of CCR5 (OR = 2.24, P = 0.0051 for carrier of both RA associated alleles) 19538721 2009
CUI: C0002871
Disease: Anemia
Anemia
0.020 Biomarker disease BEFREE Most Dnase1 and Dnase2 family members are poorly characterized, yet their elimination can lead to a wide range of diseases, including lethal anemia, parakeratosis, cataracts and systemic lupus erythematosus. 28666955 2017
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.330 Biomarker disease BEFREE Most Dnase1 and Dnase2 family members are poorly characterized, yet their elimination can lead to a wide range of diseases, including lethal anemia, parakeratosis, cataracts and systemic lupus erythematosus. 28666955 2017
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.100 GeneticVariation phenotype GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 Biomarker disease BEFREE Our data suggest that the SNPs in DNL genes may serve as independent prognostic markers for NSCLC patients after surgery. 25227797 2014
CUI: C3267073
Disease: Autoinflammatory disease
Autoinflammatory disease
0.010 GeneticVariation disease BEFREE Patients with hypomorphic mutations in DNase II develop a severe and debilitating autoinflammatory disease. 31464028 2020