Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22954
Gene Symbol: TRIM32
TRIM32
0.720 GeneticVariation disease BEFREE A mutation in the B-box region of TRIM32 has also been shown to result in a more pleiotropic disorder, Bardet-Biedl Syndrome (BBS11). 21496629 2011
Entrez Id: 22954
Gene Symbol: TRIM32
TRIM32
0.720 Biomarker disease BEFREE Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). 16606853 2006
Entrez Id: 22954
Gene Symbol: TRIM32
TRIM32
0.720 Biomarker disease GENOMICS_ENGLAND Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). 16606853 2006
Entrez Id: 22954
Gene Symbol: TRIM32
TRIM32
0.720 GeneticVariation disease UNIPROT Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). 16606853 2006
Entrez Id: 22954
Gene Symbol: TRIM32
TRIM32
0.720 Biomarker disease GENOMICS_ENGLAND Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene. 11822024 2002
Entrez Id: 22954
Gene Symbol: TRIM32
TRIM32
0.720 GeneticVariation disease CLINVAR
Entrez Id: 22954
Gene Symbol: TRIM32
TRIM32
0.720 CausalMutation disease CLINVAR
Entrez Id: 22954
Gene Symbol: TRIM32
TRIM32
0.720 Biomarker disease CTD_human
Entrez Id: 23245
Gene Symbol: ASTN2
ASTN2
0.100 CausalMutation disease CLINVAR
Entrez Id: 23245
Gene Symbol: ASTN2
ASTN2
0.100 GeneticVariation disease CLINVAR
Entrez Id: 79594
Gene Symbol: MUL1
MUL1
0.010 Biomarker disease BEFREE Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). 16606853 2006
Entrez Id: 5071
Gene Symbol: PRKN
PRKN
0.010 Biomarker disease BEFREE Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). 16606853 2006
Entrez Id: 158506
Gene Symbol: CBLL2
CBLL2
0.010 Biomarker disease BEFREE Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). 16606853 2006