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: 29842
Gene Symbol: TFCP2L1
TFCP2L1 		transcription factor CP2 like 1 0.751 0.346 1.00
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 51460
Gene Symbol: SFMBT1
SFMBT1 		Scm like with four mbt domains 1 0.736 0.385 0.94
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 51684
Gene Symbol: SUFU
SUFU 		SUFU negative regulator of hedgehog signaling 0.493 0.769 1.00
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 51755
Gene Symbol: CDK12
CDK12 		cyclin dependent kinase 12 0.638 0.462 1.00
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7 		protein arginine methyltransferase 7 0.674 0.538 5.5E-15
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 54617
Gene Symbol: INO80
INO80 		INO80 complex ATPase subunit 0.751 0.385 1.00
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 2 2016 2016
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9 		solute carrier family 2 member 9 0.619 0.731 6.9E-10
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 57157
Gene Symbol: PHTF2
PHTF2 		putative homeodomain transcription factor 2 1.000 0.077 1.8E-04
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2016 2016
Entrez Id: 57158
Gene Symbol: JPH2
JPH2 		junctophilin 2 0.736 0.154 4.5E-05
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2016 2016
Entrez Id: 57214
Gene Symbol: CEMIP
CEMIP 		cell migration inducing hyaluronidase 1 0.617 0.615 4.4E-17
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 57591
Gene Symbol: MRTFA
MRTFA 		myocardin related transcription factor A 0.572 0.615 1.00
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 5119
Gene Symbol: CHMP1A
CHMP1A 		charged multivesicular body protein 1A 0.695 0.500 2.9E-04
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1 		nuclear factor kappa B subunit 1 0.396 0.923 1.00
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 29956
Gene Symbol: CERS2
CERS2 		ceramide synthase 2 0.691 0.500 0.48
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 3117
Gene Symbol: HLA-DQA1
HLA-DQA1 		major histocompatibility complex, class II, DQ alpha 1 0.416 0.846 2.4E-02
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 3236
Gene Symbol: HOXD10
HOXD10 		homeobox D10 0.590 0.538 6.3E-02
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 3237
Gene Symbol: HOXD11
HOXD11 		homeobox D11 0.670 0.462 1.1E-03
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 3626
Gene Symbol: INHBC
INHBC 		inhibin subunit beta C 0.792 0.423 5.6E-05
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		arginase 1 0.476 0.846 3.6E-04
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 389
Gene Symbol: RHOC
RHOC 		ras homolog family member C 0.641 0.308 0.77
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 4026
Gene Symbol: LPP
LPP 		LIM domain containing preferred translocation partner in lipoma 0.543 0.769 7.2E-03
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 4092
Gene Symbol: SMAD7
SMAD7 		SMAD family member 7 0.470 0.769 0.55
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 4126
Gene Symbol: MANBA
MANBA 		mannosidase beta 0.736 0.462 1.3E-18
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2016 2016
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B 		myosin heavy chain 7B 0.792 0.308 4.3E-46
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 58528
Gene Symbol: RRAGD
RRAGD 		Ras related GTP binding D 0.82
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		phenotype 0.100 None 1.000 1 1 2018 2018