Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.010 Biomarker group BEFREE Here, we report that myocardial-specific deletion of <i>Jarid2</i> using α<i>MHC</i>::<i>Cre</i> mice (<i>Jarid2</i><sup>αMHC</sup>) causes dilated cardiomyopathy (DCM) and premature death 6-9 months after birth. 30700554 2019
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 Biomarker disease BEFREE Dihydroartemisinin inhibits prostate cancer via JARID2/miR-7/miR-34a-dependent downregulation of Axl. 30783079 2019
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 AlteredExpression phenotype BEFREE Downregulation of Jarid2 with shRNA transfection obviously inhibited the proliferation, migration and tumorigenesis of bladder cancer T24 and HT-1376 cells and induced cell apoptosis. 31125562 2019
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 Biomarker disease BEFREE Dihydroartemisinin inhibits prostate cancer via JARID2/miR-7/miR-34a-dependent downregulation of Axl. 30783079 2019
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
0.010 Biomarker disease BEFREE To determine functions of Jarid2 in the adult heart and DCM, we analyzed gene expression in the heart at postnatal day (p)10 (neonatal) and 7 months (DCM). 30700554 2019
CUI: C0280449
Disease: secondary acute myeloid leukemia
secondary acute myeloid leukemia
0.010 GeneticVariation disease BEFREE Genetic deletion of Jarid2 either reduced overall survival of animals with MPNs or drove transformation to sAML, depending on the timing and context of co-operating mutations. 30423295 2018
CUI: C0376544
Disease: Hematopoietic Neoplasms
Hematopoietic Neoplasms
0.010 Biomarker group BEFREE These studies establish JARID2 as a bona fide hematopoietic tumor suppressor and highlight potential therapeutic targets. 30423295 2018
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder
0.010 GeneticVariation group BEFREE A study of single nucleotide polymorphisms in CD157, AIM2 and JARID2 genes in Han Chinese children with autism spectrum disorder. 29216786 2018
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
0.010 GeneticVariation disease BEFREE Genetic deletion of Jarid2 either reduced overall survival of animals with MPNs or drove transformation to sAML, depending on the timing and context of co-operating mutations. 30423295 2018
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME
0.010 Biomarker group BEFREE JARID2 is lost by chromosomal deletions in a proportion of MPN/MDS cases that progress to sAML. 30423295 2018
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
0.010 GeneticVariation disease BEFREE Four SNPs in CRISPLD2 (rs1546124, rs8061351, rs2326398, and rs4783099) and four in JARID2 (rs915344, rs2299043, rs2237138, and rs2076056), that were previously reported to be associated with NSCL/P, were genotyped in 785 Brazilian patients with NSCL/P (549 with cleft lip with or without cleft palate-NSCL ± P, and 236 with cleft palate only-NSCPO) and 693 unaffected Brazilian controls. 27328068 2017
CUI: C0009319
Disease: Colitis
Colitis
0.010 Biomarker disease BEFREE MiR-155 contributes to Th17 cells differentiation in dextran sulfate sodium (DSS)-induced colitis mice via Jarid2. 28461115 2017
CUI: C0017638
Disease: Glioma
Glioma
0.010 Biomarker disease BEFREE Therefore, JARID2 may serve as a potential therapeutic target for the treatment of glioma. 27641964 2017
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 Biomarker disease BEFREE The expression of MEG3 long noncoding RNA (lncRNA), which could interact with JARID2, was clearly increased during transforming growth factor-β (TGF-β)-induced EMT of human lung cancer cell lines. 27852821 2017
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 Biomarker disease BEFREE The expression of MEG3 long noncoding RNA (lncRNA), which could interact with JARID2, was clearly increased during transforming growth factor-β (TGF-β)-induced EMT of human lung cancer cell lines. 27852821 2017
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.010 Biomarker disease BEFREE Therefore, JARID2 may represent a potential therapeutic target for the treatment of ovarian cancer. 28765957 2017
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.010 Biomarker disease BEFREE Therefore, JARID2 may represent a potential therapeutic target for the treatment of ovarian cancer. 28765957 2017
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 Biomarker disease BEFREE The expression of MEG3 long noncoding RNA (lncRNA), which could interact with JARID2, was clearly increased during transforming growth factor-β (TGF-β)-induced EMT of human lung cancer cell lines. 27852821 2017
CUI: C1837218
Disease: Cleft palate, isolated
Cleft palate, isolated
0.010 GeneticVariation disease BEFREE Four SNPs in CRISPLD2 (rs1546124, rs8061351, rs2326398, and rs4783099) and four in JARID2 (rs915344, rs2299043, rs2237138, and rs2076056), that were previously reported to be associated with NSCL/P, were genotyped in 785 Brazilian patients with NSCL/P (549 with cleft lip with or without cleft palate-NSCL ± P, and 236 with cleft palate only-NSCPO) and 693 unaffected Brazilian controls. 27328068 2017
CUI: C2981150
Disease: Uranostaphyloschisis
Uranostaphyloschisis
0.010 GeneticVariation disease BEFREE Four SNPs in CRISPLD2 (rs1546124, rs8061351, rs2326398, and rs4783099) and four in JARID2 (rs915344, rs2299043, rs2237138, and rs2076056), that were previously reported to be associated with NSCL/P, were genotyped in 785 Brazilian patients with NSCL/P (549 with cleft lip with or without cleft palate-NSCL ± P, and 236 with cleft palate only-NSCPO) and 693 unaffected Brazilian controls. 27328068 2017
CUI: C4021813
Disease: Oral cleft
Oral cleft
0.010 GeneticVariation disease BEFREE Haplotype analysis indicated a lack of association between JARID2 haplotypes and non-syndromic oral cleft risk. 27328068 2017
Abnormality of cardiovascular system morphology
0.010 GeneticVariation disease BEFREE Within our clinical cohort, we also observed heterozygous LOF variants in JARID2 and SMAD1 in individuals with cardiac phenotypes, and collectively, carriers of LOF variants in our candidate genes had a four times higher odds of having CVM (odds ratio = 4.0, 95% confidence interval 2.5-6.5). 29089047 2017
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.010 Biomarker disease BEFREE Therefore, JARID2 may represent a potential therapeutic target for the treatment of ovarian cancer. 28765957 2017
CUI: C0023418
Disease: leukemia
leukemia
0.010 Biomarker disease BEFREE Our findings indicate that JARID2 is a negative regulator of leukemia cell proliferation, and functions as potential tumor suppressor in leukemia. 25939703 2015
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.010 AlteredExpression disease BEFREE JARID2 is down-regulated in B-chronic lymphocytic leukemia (B-CLL) and acute monocytic leukemia (AMOL), and knockdown of JARID2 promotes leukemia cell proliferation via acceleration of the G1/S transition. 25939703 2015