Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9 		0.100 Biomarker phenotype HPO
Entrez Id: 60
Gene Symbol: ACTB
ACTB 		0.100 Biomarker phenotype HPO
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1 		0.400 Biomarker phenotype HPO
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1 		0.400 Biomarker phenotype GENOMICS_ENGLAND FISH localization of human cytoplasmic actin genes ACTB to 7p22 and ACTG1 to 17q25 and characterization of related pseudogenes. 8941379 1996
Entrez Id: 54806
Gene Symbol: AHI1
AHI1 		0.100 Biomarker phenotype HPO
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11 		0.100 Biomarker phenotype HPO
Entrez Id: 200894
Gene Symbol: ARL13B
ARL13B 		0.100 Biomarker phenotype HPO
Entrez Id: 403
Gene Symbol: ARL3
ARL3 		0.100 Biomarker phenotype HPO
Entrez Id: 80210
Gene Symbol: ARMC9
ARMC9 		0.100 Biomarker phenotype HPO
Entrez Id: 259266
Gene Symbol: ASPM
ASPM 		0.100 Biomarker phenotype HPO
Entrez Id: 55252
Gene Symbol: ASXL2
ASXL2 		0.100 Biomarker phenotype HPO
Entrez Id: 80816
Gene Symbol: ASXL3
ASXL3 		0.100 Biomarker phenotype HPO
Entrez Id: 80816
Gene Symbol: ASXL3
ASXL3 		0.100 CausalMutation phenotype CLINVAR Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome. 27075689 2016
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2 		0.100 Biomarker phenotype HPO
Entrez Id: 27077
Gene Symbol: B9D1
B9D1 		0.100 Biomarker phenotype HPO
Entrez Id: 54880
Gene Symbol: BCOR
BCOR 		0.100 Biomarker phenotype HPO
Entrez Id: 613
Gene Symbol: BCR
BCR 		0.100 Biomarker phenotype HPO
Entrez Id: 113246
Gene Symbol: C12orf57
C12orf57 		0.100 Biomarker phenotype HPO
Entrez Id: 818
Gene Symbol: CAMK2G
CAMK2G 		0.100 Biomarker phenotype HPO
Entrez Id: 57545
Gene Symbol: CC2D2A
CC2D2A 		0.100 Biomarker phenotype HPO
Entrez Id: 998
Gene Symbol: CDC42
CDC42 		0.100 Biomarker phenotype HPO
Entrez Id: 1009
Gene Symbol: CDH11
CDH11 		0.100 Biomarker phenotype HPO
Entrez Id: 8621
Gene Symbol: CDK13
CDK13 		0.100 GeneticVariation phenotype CLINVAR Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders. 28807008 2017
Entrez Id: 9731
Gene Symbol: CEP104
CEP104 		0.100 Biomarker phenotype HPO
Entrez Id: 153241
Gene Symbol: CEP120
CEP120 		0.100 Biomarker phenotype HPO