Source: MGD

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 55
Gene Symbol: ACP3
ACP3 		acid phosphatase 3 0.525 0.731 2.5E-16
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		disease 0.300 None 1.000 2 0 1981 2019
Entrez Id: 58
Gene Symbol: ACTA1
ACTA1 		actin alpha 1, skeletal muscle 0.540 0.769 1.1E-06
CUI: C1834339
Disease: Myopathy, Actin, Congenital, with Excess of Thin Myofilaments
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments 		disease 0.600 strong 1.000 1 0 2009 2011
Entrez Id: 58
Gene Symbol: ACTA1
ACTA1 		actin alpha 1, skeletal muscle 0.540 0.769 1.1E-06
CUI: C2750536
Disease: Nemaline Myopathy 3, With Intranuclear Rods
Nemaline Myopathy 3, With Intranuclear Rods 		disease 0.200 None 1.000 1 0 2011 2011
Entrez Id: 58
Gene Symbol: ACTA1
ACTA1 		actin alpha 1, skeletal muscle 0.540 0.769 1.1E-06
CUI: C2750537
Disease: Myopathy, Actin, Congenital, With Cores
Myopathy, Actin, Congenital, With Cores 		disease 0.600 strong 1.000 1 0 2009 2011
Entrez Id: 58
Gene Symbol: ACTA1
ACTA1 		actin alpha 1, skeletal muscle 0.540 0.769 1.1E-06
CUI: C3711389
Disease: Actin-Accumulation Myopathy
Actin-Accumulation Myopathy 		disease 0.930 None 1.000 1 0 1988 2018
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1 		actin alpha cardiac muscle 1 0.610 0.538 0.74
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		group 0.650 None 1.000 0 0 2006 2019
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1 		actin alpha cardiac muscle 1 0.610 0.538 0.74
CUI: C3150681
Disease: CARDIOMYOPATHY, DILATED, 1R
CARDIOMYOPATHY, DILATED, 1R 		disease 0.800 strong 1.000 0 0 1998 2019
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1 		actin alpha cardiac muscle 1 0.610 0.538 0.74
CUI: C3150682
Disease: LEFT VENTRICULAR NONCOMPACTION 4
LEFT VENTRICULAR NONCOMPACTION 4 		disease 0.600 strong 0 0
Entrez Id: 10093
Gene Symbol: ARPC4
ARPC4 		actin related protein 2/3 complex subunit 4 0.780 0.269 0.97
CUI: C0033860
Disease: Psoriasis
Psoriasis 		disease 0.200 None 0 0
Entrez Id: 81
Gene Symbol: ACTN4
ACTN4 		actinin alpha 4 0.508 0.808 1.00
CUI: C0451720
Disease: Nephrotic syndrome, focal and segmental glomerular lesions
Nephrotic syndrome, focal and segmental glomerular lesions 		disease 0.200 None 1.000 3 0 2003 2007
Entrez Id: 81
Gene Symbol: ACTN4
ACTN4 		actinin alpha 4 0.508 0.808 1.00
CUI: C2902887
Disease: Nephrotic syndrome with focal and segmental hyalinosis
Nephrotic syndrome with focal and segmental hyalinosis 		disease 0.200 None 1.000 3 0 2003 2007
Entrez Id: 81
Gene Symbol: ACTN4
ACTN4 		actinin alpha 4 0.508 0.808 1.00
CUI: C2902888
Disease: Nephrotic syndrome with focal and segmental sclerosis
Nephrotic syndrome with focal and segmental sclerosis 		disease 0.200 None 1.000 3 0 2003 2007
Entrez Id: 81
Gene Symbol: ACTN4
ACTN4 		actinin alpha 4 0.508 0.808 1.00
CUI: C2902889
Disease: Nephrotic syndrome with focal glomerulonephritis
Nephrotic syndrome with focal glomerulonephritis 		disease 0.200 None 1.000 3 0 2003 2007
Entrez Id: 81
Gene Symbol: ACTN4
ACTN4 		actinin alpha 4 0.508 0.808 1.00
CUI: C4551527
Disease: Focal segmental glomerulosclerosis 1
Focal segmental glomerulosclerosis 1 		disease 0.800 strong 1.000 3 0 2000 2015
Entrez Id: 1386
Gene Symbol: ATF2
ATF2 		activating transcription factor 2 0.551 0.808 0.99
CUI: C0008449
Disease: Congenital anomaly of cartilage
Congenital anomaly of cartilage 		group 0.200 None 0 0
Entrez Id: 1386
Gene Symbol: ATF2
ATF2 		activating transcription factor 2 0.551 0.808 0.99
CUI: C0025048
Disease: Meconium Aspiration Syndrome
Meconium Aspiration Syndrome 		phenotype 0.210 None 1.000 0 0 1999 1999
Entrez Id: 1386
Gene Symbol: ATF2
ATF2 		activating transcription factor 2 0.551 0.808 0.99
CUI: C0029422
Disease: Osteochondrodysplasias
Osteochondrodysplasias 		group 0.200 None 0 0
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2 		activator of transcription and developmental regulator AUTS2 0.569 0.846 1.00
CUI: C4014435
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 		disease 0.800 None 1.000 2 0 2013 2015
Entrez Id: 94
Gene Symbol: ACVRL1
ACVRL1 		activin A receptor like type 1 0.493 0.769 9.7E-04
CUI: C0039445
Disease: Hereditary hemorrhagic telangiectasia
Hereditary hemorrhagic telangiectasia 		disease 0.600 None 1.000 1 0 1996 2019
Entrez Id: 94
Gene Symbol: ACVRL1
ACVRL1 		activin A receptor like type 1 0.493 0.769 9.7E-04
CUI: C0007772
Disease: Intracranial Arteriovenous Malformation
Intracranial Arteriovenous Malformation 		disease 0.200 None 0 0
Entrez Id: 90
Gene Symbol: ACVR1
ACVR1 		activin A receptor type 1 0.535 0.731 0.33
CUI: C0016037
Disease: Fibrodysplasia Ossificans Progressiva
Fibrodysplasia Ossificans Progressiva 		disease 1.000 None 1.000 1 0 2006 2020
Entrez Id: 92
Gene Symbol: ACVR2A
ACVR2A 		activin A receptor type 2A 0.636 0.615 1.00
CUI: C0031900
Disease: Pierre Robin Syndrome
Pierre Robin Syndrome 		disease 0.200 None 1.000 1 0 1995 1995
Entrez Id: 93
Gene Symbol: ACVR2B
ACVR2B 		activin A receptor type 2B 0.601 0.615 0.83
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		disease 0.500 None 1.000 1 0 1997 1999
Entrez Id: 93
Gene Symbol: ACVR2B
ACVR2B 		activin A receptor type 2B 0.601 0.615 0.83
CUI: C0265357
Disease: Polysplenia Syndrome
Polysplenia Syndrome 		disease 0.500 None 1.000 1 0 1997 1999
Entrez Id: 93
Gene Symbol: ACVR2B
ACVR2B 		activin A receptor type 2B 0.601 0.615 0.83
CUI: C0344692
Disease: Isomerism of atrial appendages
Isomerism of atrial appendages 		disease 0.200 None 1.000 1 0 1997 1997