Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 404672
Gene Symbol: GTF2H5
GTF2H5
0.100 Biomarker phenotype HPO
Entrez Id: 6439
Gene Symbol: SFTPB
SFTPB
0.100 Biomarker phenotype HPO
Entrez Id: 727897
Gene Symbol: MUC5B
MUC5B
0.100 Biomarker phenotype HPO
Entrez Id: 6440
Gene Symbol: SFTPC
SFTPC
0.100 Biomarker phenotype HPO
Entrez Id: 729238
Gene Symbol: SFTPA2
SFTPA2
0.100 Biomarker phenotype HPO
Entrez Id: 6794
Gene Symbol: STK11
STK11
0.100 Biomarker phenotype HPO
Entrez Id: 7737
Gene Symbol: RNF113A
RNF113A
0.100 Biomarker phenotype HPO
Entrez Id: 7015
Gene Symbol: TERT
TERT
0.100 Biomarker phenotype HPO
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
0.100 Biomarker phenotype HPO
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
0.100 Biomarker phenotype HPO
Entrez Id: 6462
Gene Symbol: SHBG
SHBG
0.010 GeneticVariation phenotype BEFREE We therefore measured estrogens, androgens, sex hormone-binding globulin (SHBG), and gonadotropins in five patients with HOA and in 18 patients with simple clubbing. 29480386 2019
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
0.010 GeneticVariation phenotype BEFREE Fifteen 2,4-thiazolidinedione derivatives clubbed with pyrazole moiety were docked into the ligand binding domain of PPAR-γ by the Glide XP module of Schrodinger. 29400412 2018
Entrez Id: 450095
Gene Symbol: PLF
PLF
0.010 Biomarker phenotype BEFREE Digital Clubbing Is Associated with Higher Serum KL-6 Levels and Lower Pulmonary Function in Patients with Interstitial Lung Disease. 29610629 2018
Entrez Id: 1565
Gene Symbol: CYP2D6
CYP2D6
0.010 Biomarker phenotype BEFREE In subjects with urinary MDMA detected post-clubbing, there was a significant association between change in plasma osmolality (p = 0.009) and in plasma sodium (p = 0.012) and CYP2D6 genotypic category. 22303032 2012
Entrez Id: 1311
Gene Symbol: COMP
COMP
0.010 GeneticVariation phenotype BEFREE The disorders include "classic MED" (Ribbing and Fairbank types): MED that is caused by mutations in the cartilage oligomeric matrix protein (COMP), type IX collagen, and matrilin 3 genes (MATN3); and MED with multilayered patella, brachydactyly, and clubbed feet resultant from mutations in gene defect diastrophic dysplasia (DTDST). 15503005 2005
Entrez Id: 4148
Gene Symbol: MATN3
MATN3
0.010 GeneticVariation phenotype BEFREE The disorders include "classic MED" (Ribbing and Fairbank types): MED that is caused by mutations in the cartilage oligomeric matrix protein (COMP), type IX collagen, and matrilin 3 genes (MATN3); and MED with multilayered patella, brachydactyly, and clubbed feet resultant from mutations in gene defect diastrophic dysplasia (DTDST). 15503005 2005