Source: ANIMAL_MODELS

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: 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: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24
zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss
disease 0.200 None 0 0
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24
zinc metallopeptidase STE24 0.517 0.731 8.9E-16
Familial Partial Lipodystrophy, Type 1
disease 0.200 None 0 0
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24
zinc metallopeptidase STE24 0.517 0.731 8.9E-16
Familial Partial Lipodystrophy, Type 2
disease 0.200 None 0 0
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24
zinc metallopeptidase STE24 0.517 0.731 8.9E-16
Familial Partial Lipodystrophy, Type 3
disease 0.200 None 0 0
Entrez Id: 10278
Gene Symbol: EFS
EFS
embryonal Fyn-associated substrate 0.597 0.615 1.8E-08
CUI: C0156147
Disease: Crohn's disease of large bowel
Crohn's disease of large bowel
disease 0.200 None 0 0
Entrez Id: 10283
Gene Symbol: CWC27
CWC27
CWC27 spliceosome associated cyclophilin 0.722 0.346 4.6E-07
CUI: C0220701
Disease: RETINITIS PIGMENTOSA 1
RETINITIS PIGMENTOSA 1
disease 0.200 None 0 0
Entrez Id: 10295
Gene Symbol: BCKDK
BCKDK
branched chain keto acid dehydrogenase kinase 0.769 0.154 5.7E-05
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
disease 0.200 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1
T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
disease 0.200 None 0 0
Entrez Id: 1051
Gene Symbol: CEBPB
CEBPB
CCAAT enhancer binding protein beta 0.508 0.731 0.36
CUI: C0003723
Disease: Arbovirus Infections
Arbovirus Infections
group 0.200 None 0 0
Entrez Id: 10533
Gene Symbol: ATG7
ATG7
autophagy related 7 0.505 0.769 7.4E-12
CUI: C2713368
Disease: Hematopoetic Myelodysplasia
Hematopoetic Myelodysplasia
phenotype 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline
disease 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
group 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
CUI: C0270962
Disease: Multi-core congenital myopathy
Multi-core congenital myopathy
disease 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion
disease 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
CUI: C0751951
Disease: Central Core Myopathy (disorder)
Central Core Myopathy (disorder)
disease 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4
disease 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
CUI: C2875316
Disease: Myotubular (centronuclear) myopathy
Myotubular (centronuclear) myopathy
disease 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3
disease 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2
disease 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14
disease 0.200 None 0 0
Entrez Id: 10585
Gene Symbol: POMT1
POMT1
protein O-mannosyltransferase 1 0.525 0.615 4.2E-17
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12
disease 0.200 None 0 0
Entrez Id: 10628
Gene Symbol: TXNIP
TXNIP
thioredoxin interacting protein 0.490 0.731 0.16
CUI: C0035400
Disease: Reye Syndrome
Reye Syndrome
disease 0.200 None 0 0
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
centromere protein F 0.601 0.654 1.9E-36
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
group 0.200 None 0 0
Entrez Id: 10640
Gene Symbol: EXOC5
EXOC5
exocyst complex component 5 0.805 0.269 1.00
CUI: C0149939
Disease: Obstructive nephropathy
Obstructive nephropathy
disease 0.200 None 0 0