Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
0.610 GeneticVariation disease BEFREE The six pathogenic variations were identified on the genes CHD7 (CHARGE syndrome), CITED2 (tetralogy of Fallot, ventricular septal defect and atrial septal defect), ZFPM2 (tetralogy of Fallot), MYH6 (atrial septal defect, familial isolated dilated cardiomyopathy) and, in two cases, KMT2D (Kabuki syndrome). 29536580 2018
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
0.610 Biomarker disease MGD The essential role of Cited2, a negative regulator for HIF-1alpha, in heart development and neurulation. 12149478 2002
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
0.610 SusceptibilityMutation disease ORPHANET
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
0.610 Biomarker disease HPO
CUI: C3280790
Disease: ATRIAL SEPTAL DEFECT 8
ATRIAL SEPTAL DEFECT 8
0.500 Biomarker disease GENOMICS_ENGLAND Variations of CITED2 are associated with congenital heart disease (CHD) in Chinese population. 24848765 2014
CUI: C3280790
Disease: ATRIAL SEPTAL DEFECT 8
ATRIAL SEPTAL DEFECT 8
0.500 Biomarker disease CTD_human
CUI: C3280790
Disease: ATRIAL SEPTAL DEFECT 8
ATRIAL SEPTAL DEFECT 8
0.500 Biomarker disease GENOMICS_ENGLAND
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.360 Biomarker group BEFREE The present study assessed the effects of CITED2 silencing on macrophage recruitment in two xenograft mouse models of human breast cancer, one in which tumor growth was sensitive to CITED2 silencing (MDA-MB-231) and one in which it was insensitive (MDA-MB-468). 29399152 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.360 Biomarker group BEFREE Here, we show that CITED2 silencing significantly attenuated MDA-MB-231 primary tumor growth concordant with reduced tumor vascularization, while MDA-MB-468 primary tumor growth and tumor vascularization remained unaffected. 28008154 2017
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.360 AlteredExpression group BEFREE Extending these studies to human breast cancer, it was observed that CITED2 mRNA expression was significantly elevated in patient specimens of metastatic breast cancer relative to primary tumors, with highest levels in metastasis to bone relative to non-bone sites. 27216153 2016
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.360 Biomarker group BEFREE Moreover, lentivirus-based CITED2 silencing sensitized HeLa cell line-derived tumor xenografts to cisplatin in immune-deficient mice. 26384430 2015
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.360 AlteredExpression group BEFREE In CEA/Tag mice, LBH589 induced tumor-cell expression of CITED2 and increased the efficacy of anthracycline to reduce tumor growth. 22465428 2012
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.360 Biomarker group CTD_human Knockdown of CITED2 using short-hairpin RNA sensitizes cancer cells to cisplatin through stabilization of p53 and enhancement of p53-dependent apoptosis. 21660965 2011
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.360 AlteredExpression group BEFREE Both NCOR2 and CITED2 mRNA levels were associated with MFS, that is, tumour aggressiveness, independently of traditional prognostic factors. 19904269 2009
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.330 Biomarker group BEFREE The role of CITED2 has been investigated in a number of malignancies; however, the roles of this protein in gastric cancers remain unclear. 28501104 2017
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.330 Biomarker group BEFREE The CITED2/p300/p53/ERCC1 pathway is thus involved in the cell response to cisplatin and represents a potential target for cancer therapy. 26384430 2015
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.330 AlteredExpression group BEFREE We found the CBP/p300-interacting transactivator with glutamic acid/asparagine-rich carboxy-terminal domain 2 (CITED2) to be specifically upregulated in UC-associated cancer cell lines by BA treatment, at both mRNA and protein expression levels. 21165656 2011
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.330 Biomarker group CTD_human In the present study, we examined whether CITED2 is also involved in the resistance of cancer cells to the chemotherapeutic drug cisplatin. 21660965 2011
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.310 Biomarker group BEFREE They also indicate that smad2, cited2, and p300 may play important roles in modulating the confirmation of ventricular septal defects. 23899608 2013
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects
0.310 Biomarker group CTD_human In summary, the observation of these mutations in patients with septal defects indicates that CITED2 has a causative impact in the development of CHD in humans. 16287139 2005
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects
0.310 GeneticVariation group BEFREE In summary, the observation of these mutations in patients with septal defects indicates that CITED2 has a causative impact in the development of CHD in humans. 16287139 2005
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.310 Biomarker group CTD_human
CUI: C0086692
Disease: Benign Neoplasm
Benign Neoplasm
0.300 Biomarker group CTD_human Knockdown of CITED2 using short-hairpin RNA sensitizes cancer cells to cisplatin through stabilization of p53 and enhancement of p53-dependent apoptosis. 21660965 2011
CUI: C0026846
Disease: Muscular Atrophy
Muscular Atrophy
0.300 Therapeutic phenotype CTD_human These results suggest that the gain of Cited2 function counteracts glucocorticoid-induced muscle atrophy through inhibition of proteolysis mediated by p300-dependent gene transcription. 19032942 2009
CUI: C0270948
Disease: Neurogenic Muscular Atrophy
Neurogenic Muscular Atrophy
0.300 Therapeutic phenotype CTD_human Overexpression of the transcriptional coregulator Cited2 protects against glucocorticoid-induced atrophy of C2C12 myotubes. 19032942 2009