Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
0.100 Biomarker disease HPO
Entrez Id: 5264
Gene Symbol: PHYH
PHYH
0.100 Biomarker disease HPO
Entrez Id: 4540
Gene Symbol: ND5
ND5
0.100 Biomarker disease HPO
Entrez Id: 4513
Gene Symbol: COX2
COX2
0.100 Biomarker disease HPO
Entrez Id: 5191
Gene Symbol: PEX7
PEX7
0.100 Biomarker disease HPO
Entrez Id: 4564
Gene Symbol: TRNH
TRNH
0.100 Biomarker disease HPO
Entrez Id: 4535
Gene Symbol: ND1
ND1
0.100 Biomarker disease HPO
Entrez Id: 4572
Gene Symbol: TRNQ
TRNQ
0.100 Biomarker disease HPO
Entrez Id: 4558
Gene Symbol: TRNF
TRNF
0.100 Biomarker disease HPO
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.100 Biomarker disease HPO
Entrez Id: 4538
Gene Symbol: ND4
ND4
0.100 Biomarker disease HPO
Entrez Id: 4514
Gene Symbol: COX3
COX3
0.100 Biomarker disease HPO
Entrez Id: 4574
Gene Symbol: TRNS1
TRNS1
0.100 Biomarker disease HPO
Entrez Id: 4541
Gene Symbol: ND6
ND6
0.100 Biomarker disease HPO
Entrez Id: 4567
Gene Symbol: TRNL1
TRNL1
0.100 Biomarker disease HPO
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3
0.100 CausalMutation disease CLINVAR
Entrez Id: 11155
Gene Symbol: LDB3
LDB3
0.100 Biomarker disease HPO
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
0.100 Biomarker disease HPO
Entrez Id: 4512
Gene Symbol: COX1
COX1
0.100 Biomarker disease HPO
Entrez Id: 4575
Gene Symbol: TRNS2
TRNS2
0.100 Biomarker disease HPO
Entrez Id: 4578
Gene Symbol: TRNW
TRNW
0.100 Biomarker disease HPO
Entrez Id: 6737
Gene Symbol: TRIM21
TRIM21
0.020 Biomarker disease BEFREE Isolated heart block in children, often associated with maternal autoimmune disease leading to anti-Ro/SS-A auto-antibody production, is an infrequent but potentially lethal disorder. 8195531 1994
Entrez Id: 4179
Gene Symbol: CD46
CD46
0.010 AlteredExpression disease BEFREE To examine fetal characteristics which might influence autoantibody-mediated diseases acquired in utero, such as heart block in neonatal lupus, the tissue expression of MCP was studied. 8528226 1995
Entrez Id: 822
Gene Symbol: CAPG
CAPG
0.010 AlteredExpression disease BEFREE To examine fetal characteristics which might influence autoantibody-mediated diseases acquired in utero, such as heart block in neonatal lupus, the tissue expression of MCP was studied. 8528226 1995
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
0.330 GeneticVariation disease BEFREE A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block. 11525883 2001