Source: ALL

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: 254251
Gene Symbol: LCORL
LCORL
ligand dependent nuclear receptor corepressor like 0.98
CUI: C0005890
Disease: Body Height
Body Height
phenotype 0.100 10 18 2008 2017
Entrez Id: 100874203
Gene Symbol: COL4A2-AS1
COL4A2-AS1
COL4A2 antisense RNA 1
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
group 0.100 7 1 2012 2016
Entrez Id: 91461
Gene Symbol: PKDCC
PKDCC
protein kinase domain containing, cytoplasmic 1.2E-04
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
group 0.100 5 2 2009 2014
Entrez Id: 100506025
Gene Symbol: ISPD-AS1
ISPD-AS1
ISPD antisense RNA 1 0.928
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7
disease 0.100 5 2 1998 2017
Entrez Id: 9489
Gene Symbol: PGS1
PGS1
phosphatidylglycerophosphate synthase 1 9.9E-12
High density lipoprotein measurement
phenotype 0.100 4 3 2010 2017
Entrez Id: 85003
Gene Symbol: BFSP2-AS1
BFSP2-AS1
BFSP2 antisense RNA 1 1.000
CUI: C3808115
Disease: CATARACT 12, MULTIPLE TYPES
CATARACT 12, MULTIPLE TYPES
disease 0.100 4 2 2000 2005
Entrez Id: 113178
Gene Symbol: SCAMP4
SCAMP4
secretory carrier membrane protein 4 1.000 5.2E-03
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36
disease 0.100 4 1 2014 2017
Entrez Id: 317761
Gene Symbol: C14orf39
C14orf39
chromosome 14 open reading frame 39 4.8E-05
CUI: C0005890
Disease: Body Height
Body Height
phenotype 0.100 4 1 2010 2015
Entrez Id: 100506025
Gene Symbol: ISPD-AS1
ISPD-AS1
ISPD antisense RNA 1 0.928
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7
disease 0.100 4 2 2012 2017
Entrez Id: 100874090
Gene Symbol: SLC6A1-AS1
SLC6A1-AS1
SLC6A1 antisense RNA 1 1.000
CUI: C4085238
Disease: MYOCLONIC-ATONIC EPILEPSY
MYOCLONIC-ATONIC EPILEPSY
disease 0.100 4 2 2015 2018
Entrez Id: 6171
Gene Symbol: RPL41
RPL41
ribosomal protein L41 0.19
CUI: C0019348
Disease: Herpes Simplex Infections
Herpes Simplex Infections
group 0.030 1.000 3 0 2002 2009
Entrez Id: 9477
Gene Symbol: MED20
MED20
mediator complex subunit 20 0.33
Erythrocyte Mean Corpuscular Hemoglobin Test
phenotype 0.100 3 4 2012 2017
Entrez Id: 9477
Gene Symbol: MED20
MED20
mediator complex subunit 20 0.33
Finding of Mean Corpuscular Hemoglobin
phenotype 0.100 3 4 2012 2017
Entrez Id: 9911
Gene Symbol: TMCC2
TMCC2
transmembrane and coiled-coil domain family 2 0.30
Platelet mean volume determination (procedure)
phenotype 0.100 3 2 2009 2017
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
MSL complex subunit 3 1.00
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group 0.300 strong 3 0 2009 2017
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
Scm polycomb group protein homolog 1 5.5E-06
CUI: C0005890
Disease: Body Height
Body Height
phenotype 0.100 3 3 2008 2014
Entrez Id: 23039
Gene Symbol: XPO7
XPO7
exportin 7 1.00
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
phenotype 0.100 3 2 2010 2017
Entrez Id: 51272
Gene Symbol: BET1L
BET1L
Bet1 golgi vesicular membrane trafficking protein like 5.0E-03
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
group 0.120 1.000 3 1 2011 2014
Entrez Id: 55731
Gene Symbol: FAM222B
FAM222B
family with sequence similarity 222 member B 0.15
Erythrocyte Mean Corpuscular Hemoglobin Test
phenotype 0.100 3 28 2012 2017
Entrez Id: 55731
Gene Symbol: FAM222B
FAM222B
family with sequence similarity 222 member B 0.15
Finding of Mean Corpuscular Hemoglobin
phenotype 0.100 3 28 2012 2017
Entrez Id: 64743
Gene Symbol: WDR13
WDR13
WD repeat domain 13 0.90
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group 0.300 limited 3 0 2010 2016
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
chromodomain helicase DNA binding protein 9 1.00
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
phenotype 0.100 3 4 2014 2017
Entrez Id: 85460
Gene Symbol: ZNF518B
ZNF518B
zinc finger protein 518B 3.0E-03
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
phenotype 0.100 3 7 2009 2013
Entrez Id: 94313
Gene Symbol: AUTS5
AUTS5
Autism, susceptibility to, 5
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
group 0.030 1.000 3 0 2009 2014
Entrez Id: 147339
Gene Symbol: C18orf25
C18orf25
chromosome 18 open reading frame 25 0.90
Erythrocyte Mean Corpuscular Hemoglobin Test
phenotype 0.100 3 41 2012 2017