Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6899
Gene Symbol: TBX1
TBX1 		1.000 ChromosomalRearrangement disease ORPHANET
Entrez Id: 6899
Gene Symbol: TBX1
TBX1 		1.000 CausalMutation disease CLINVAR
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.600 ChromosomalRearrangement disease ORPHANET
Entrez Id: 2253
Gene Symbol: FGF8
FGF8 		0.500 Biomarker disease MGD
Entrez Id: 1714
Gene Symbol: DGCR
DGCR 		0.400 Biomarker disease CTD_human
Entrez Id: 8214
Gene Symbol: DGCR6
DGCR6 		0.350 Biomarker disease CTD_human
Entrez Id: 9993
Gene Symbol: DGCR2
DGCR2 		0.340 Biomarker disease CTD_human
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8 		0.340 Biomarker disease CTD_human
Entrez Id: 7353
Gene Symbol: UFD1
UFD1 		0.330 ChromosomalRearrangement disease ORPHANET
Entrez Id: 2812
Gene Symbol: GP1BB
GP1BB 		0.310 ChromosomalRearrangement disease ORPHANET
Entrez Id: 421
Gene Symbol: ARVCF
ARVCF 		0.300 ChromosomalRearrangement disease ORPHANET
Entrez Id: 8220
Gene Symbol: ESS2
ESS2 		0.300 Biomarker disease CTD_human
Entrez Id: 1793
Gene Symbol: DOCK1
DOCK1 		0.200 Biomarker disease MGD
Entrez Id: 167465
Gene Symbol: ZNF366
ZNF366 		0.200 Biomarker disease MGD
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2 		0.200 Biomarker disease MGD
Entrez Id: 3340
Gene Symbol: NDST1
NDST1 		0.200 Biomarker disease MGD
Entrez Id: 23405
Gene Symbol: DICER1
DICER1 		0.200 Biomarker disease MGD
Entrez Id: 23129
Gene Symbol: PLXND1
PLXND1 		0.200 Biomarker disease MGD
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.230 Biomarker disease MGD 'Nude', a new hairless gene with pleiotropic effects in the mouse. 5980117 1966
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.230 Biomarker disease MGD Absence of thymus in a mouse mutant. 5639157 1968
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.230 Biomarker disease MGD The lymphoid tissues in mice with congenital aplasia of the thymus. 5784127 1969
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.230 Biomarker disease MGD Thymus dysgenesis in nude (nu nu) mice. 5493276 1970
Entrez Id: 3541
Gene Symbol: IGLC5
IGLC5 		0.010 Biomarker disease BEFREE We have performed in situ hybridization of a probe for the lambda IGLC constant region to metaphase spreads from two DiGeorge syndrome (DGS)-related chromosomal rearrangements with breakpoints in 22q11. 3930157 1985
Entrez Id: 3542
Gene Symbol: IGLC6
IGLC6 		0.010 Biomarker disease BEFREE We have performed in situ hybridization of a probe for the lambda IGLC constant region to metaphase spreads from two DiGeorge syndrome (DGS)-related chromosomal rearrangements with breakpoints in 22q11. 3930157 1985
Entrez Id: 3538
Gene Symbol: IGLC2
IGLC2 		0.010 Biomarker disease BEFREE We have performed in situ hybridization of a probe for the lambda IGLC constant region to metaphase spreads from two DiGeorge syndrome (DGS)-related chromosomal rearrangements with breakpoints in 22q11. 3930157 1985