Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10058
Gene Symbol: ABCB6
ABCB6
0.010 Biomarker disease BEFREE This 2-year analysis assessed frequency of comorbidities and comorbidity screening in the Somatuline<sup>®</sup> (lanreotide, LAN) Depot for Acromegaly (SODA) registry. 29767287 2018
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.020 GeneticVariation disease BEFREE The aim of the study was to investigate the association between ACE (I/D) and AGT (M235T) gene polymorphisms and cardiovascular and metabolic disorders in the acromegaly. 28712073 2017
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.020 GeneticVariation disease BEFREE Effects of angiotensin-converting enzyme gene polymorphism on the left-ventricular function and mass in patients with acromegaly. 10844381 1999
Entrez Id: 181
Gene Symbol: AGRP
AGRP
0.010 AlteredExpression disease BEFREE The plasma AgRP levels were higher in those with active acromegaly than in the matched healthy subjects [median, 100 pg/mL; interquartile range (IQR), 78 to 139 pg/mL vs median, 63 pg/mL; IQR, 58 to 67 pg/mL; P < 0.0001]. 31361303 2019
Entrez Id: 183
Gene Symbol: AGT
AGT
0.020 GeneticVariation disease BEFREE It can be said that the angiotensinogen MT and AT1R CC1166 genotype carriers may have more risk than other genotypes in the development of hypertension in acromegaly. 20361261 2011
Entrez Id: 183
Gene Symbol: AGT
AGT
0.020 GeneticVariation disease BEFREE The controls had similar distribution of the AGT genotype with the acromegaly group (80.2% MT genotype, 15.1% MM genotype and 4.7% TT genotype). 28712073 2017
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
0.010 GeneticVariation disease BEFREE It can be said that the angiotensinogen MT and AT1R CC1166 genotype carriers may have more risk than other genotypes in the development of hypertension in acromegaly. 20361261 2011
Entrez Id: 196
Gene Symbol: AHR
AHR
0.040 GeneticVariation disease BEFREE Germline mutations in the aryl-hydrocarbon receptor (AHR) interacting protein (AIP) have been identified in familial forms of acromegaly. 25019383 2014
Entrez Id: 196
Gene Symbol: AHR
AHR
0.040 GeneticVariation disease BEFREE Increased frequency of the rs2066853 variant of aryl hydrocarbon receptor gene in patients with acromegaly. 24521362 2014
Entrez Id: 196
Gene Symbol: AHR
AHR
0.040 GeneticVariation disease BEFREE We correlated the occurrence of AHR and/or AHR-interacting protein (AIP) gene variants with acromegaly severity according to pollution exposition. 26963951 2016
Entrez Id: 196
Gene Symbol: AHR
AHR
0.040 GeneticVariation disease BEFREE GSTP1 gene methylation and AHR rs2066853 variant predict resistance to first generation somatostatin analogs in patients with acromegaly. 30488289 2019
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 GeneticVariation disease BEFREE We detected chromothripsis-related CNA profiles in two adenoma samples from an AIP mutation-positive patient with acromegaly and a patient with sporadic gigantism. 29474559 2018
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 GeneticVariation disease BEFREE Patients harboring <i>AIP</i> mutations usually present with somatotropinomas resulting either in gigantism or young-onset acromegaly. 28427099 2017
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 Biomarker disease BEFREE The prevalence of AIP(mut) in Turkish patients was found to be 1 % in sporadic acromegaly in the present study. 26021842 2015
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 Biomarker disease BEFREE Adrenal lesions in acromegaly: do metabolic aspects and aryl hydrocarbon receptor interacting protein gene have a role? Evaluation at baseline and after long-term follow-up. 20595802 2011
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 GeneticVariation disease BEFREE Germline mutations of aryl hydrocarbon receptor-interacting protein (AIP) gene and somatostatin receptor 1-5 and AIP immunostaining in patients with sporadic acromegaly with poor versus good response to somatostatin analogues. 29455389 2018
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 GeneticVariation disease BEFREE Frequency of AIP gene mutations in young patients with acromegaly: a registry-based study. 25093619 2014
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 AlteredExpression disease BEFREE AIP protein expression was similar in neoplastic and normal cells, while AHR protein was expressed more in PTCs carrying BRAF mutations than in normal tissue, irrespective of acromegaly status. 25019383 2014
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 GeneticVariation disease BEFREE Patients with AIP mutations tended to have an earlier onset of acromegaly and harboured larger and more invasive tumours. 27033541 2016
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 GeneticVariation disease BEFREE AIP mutations were detected in 16 (3.6%) of the 443 patients, comprising six of 148 patients with acromegaly (4.1%), six of 132 patients with prolactinomas (4.5%), one of 113 patients with nonfunctioning adenomas (0.9%), three of 44 patients with corticotropic adenomas (6.8%), and none of the six patients with thyrotropic adenomas. 22319033 2012
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 SusceptibilityMutation disease ORPHANET Pathogenesis of familial acromegaly. 20616502 2010
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 GeneticVariation disease BEFREE We studied two AIP-mutation positive acromegaly patients with early-onset, invasive macroadenomas and inoperable residues after neurosurgery. 30851160 2019
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 SusceptibilityMutation disease ORPHANET AIP germline mutations show a low, but non-negligible, prevalence in non-familial acromegaly patients with tumors resistant to treatment with somatostatin analogues. 23038625 2013
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 GeneticVariation disease BEFREE Germline AIP mutations usually cause young-onset acromegaly with low penetrance in a subset of familial isolated pituitary adenoma families. 24423289 2014
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.400 GeneticVariation disease BEFREE We enrolled 77 wild-type AIP gene acromegaly patients, who have been screened for germline AHR rs2066853 variant and GSTP1 gene promoter methylation. 30488289 2019