Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 GeneticVariation disease BEFREE Cyclin-dependent kinase inhibitor 1B (CDKN1B) pathogenic variants lead to multiple endocrine neoplasia type 4 (MEN4) syndrome, in which pituitary adenomas can occur. 31658440 2019
Entrez Id: 4221
Gene Symbol: MEN1
MEN1
0.010 Biomarker disease BEFREE Gastrointestinal neuroendocrine tumors appear to be less prevalent in MEN4 than in MEN1. 30990521 2019
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 GermlineCausalMutation disease ORPHANET The aim of this study was to in vitro characterize the germline CDKN1B mutation c.374_375delCT (S125X) we detected in a patient with MEN4. 25416039 2015
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 Biomarker disease GENOMICS_ENGLAND Diagnosis of asymptomatic primary hyperparathyroidism: proceedings of the Fourth International Workshop. 25162666 2014
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 GeneticVariation disease BEFREE As the CDKN1B (p27) gene causes MEN4 syndrome and it is transcriptionally regulated by the product of the MEN1 gene (menin), we sought to analyze whether p27 influences the phenotype of MEN1-mutated patients. 24920291 2014
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 Biomarker disease CLINGEN Eight mutations of CDKN1B in MEN4 patients have been published so far. 24819502 2014
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 GeneticVariation disease BEFREE Eight mutations of CDKN1B in MEN4 patients have been published so far. 24819502 2014
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 GeneticVariation disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how it is affected by MENX- or MEN4-associated mutations. 23800691 2013
Entrez Id: 100302736
Gene Symbol: TMED7-TICAM2
TMED7-TICAM2
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how it is affected by MENX- or MEN4-associated mutations. 23800691 2013
Entrez Id: 115482696
Gene Symbol: H3P23
H3P23
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how it is affected by MENX- or MEN4-associated mutations. 23800691 2013
Entrez Id: 10534
Gene Symbol: ZNRD2
ZNRD2
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how it is affected by MENX- or MEN4-associated mutations. 23800691 2013
Entrez Id: 3429
Gene Symbol: IFI27
IFI27
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how it is affected by MENX- or MEN4-associated mutations. 23800691 2013
Entrez Id: 5715
Gene Symbol: PSMD9
PSMD9
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how it is affected by MENX- or MEN4-associated mutations. 23800691 2013
Entrez Id: 51014
Gene Symbol: TMED7
TMED7
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how it is affected by MENX- or MEN4-associated mutations. 23800691 2013
Entrez Id: 10671
Gene Symbol: DCTN6
DCTN6
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how it is affected by MENX- or MEN4-associated mutations. 23800691 2013
Entrez Id: 353376
Gene Symbol: TICAM2
TICAM2
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how it is affected by MENX- or MEN4-associated mutations. 23800691 2013
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 GeneticVariation disease BEFREE Here, we review the clinical characteristics of the MEN4 syndrome and the molecular phenotype of the associated p27Kip1 mutations. 23652671 2013
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 Biomarker disease CLINGEN A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype. 23555276 2013
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B
0.790 GeneticVariation disease BEFREE A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype. 23555276 2013
Entrez Id: 115482696
Gene Symbol: H3P23
H3P23
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how they are affected by MENX/4-associated mutations. 22584700 2012
Entrez Id: 100302736
Gene Symbol: TMED7-TICAM2
TMED7-TICAM2
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how they are affected by MENX/4-associated mutations. 22584700 2012
Entrez Id: 51014
Gene Symbol: TMED7
TMED7
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how they are affected by MENX/4-associated mutations. 22584700 2012
Entrez Id: 5715
Gene Symbol: PSMD9
PSMD9
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how they are affected by MENX/4-associated mutations. 22584700 2012
Entrez Id: 10671
Gene Symbol: DCTN6
DCTN6
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how they are affected by MENX/4-associated mutations. 22584700 2012
Entrez Id: 3429
Gene Symbol: IFI27
IFI27
0.020 Biomarker disease BEFREE Here we review the characteristics of the MENX and MEN4 syndromes and we briefly address the main function of p27 and how they are affected by MENX/4-associated mutations. 22584700 2012