DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Gait Disturbance, CTCAE ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	657
Gene Symbol:	BMPR1A

BMPR1A

bone morphogenetic protein receptor type 1A

0.522

0.731

0.90

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	65998
Gene Symbol:	C11orf95

C11orf95

chromosome 11 open reading frame 95

0.780

0.115

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	83636
Gene Symbol:	C19orf12

C19orf12

chromosome 19 open reading frame 12

0.641

0.615

0.34

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	720
Gene Symbol:	C4A

C4A

complement C4A (Rodgers blood group)

0.563

0.769

1.5E-11

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	203228
Gene Symbol:	C9orf72

C9orf72

C9orf72-SMCR8 complex subunit

0.496

0.769

1.1E-06

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	767
Gene Symbol:	CA8

CA8

carbonic anhydrase 8

0.595

0.654

8.3E-03

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	825
Gene Symbol:	CAPN3

CAPN3

calpain 3

0.564

0.615

3.6E-19

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	8573
Gene Symbol:	CASK

CASK

calcium/calmodulin dependent serine protein kinase

0.538

0.808

1.00

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	57545
Gene Symbol:	CC2D2A

CC2D2A

coiled-coil and C2 domain containing 2A

0.532

0.692

1.7E-27

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	285025
Gene Symbol:	CCDC141

CCDC141

coiled-coil domain containing 141

0.666

0.538

1.6E-33

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	8838
Gene Symbol:	CCN6

CCN6

cellular communication network factor 6

0.568

0.731

6.2E-04

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	1230
Gene Symbol:	CCR1

CCR1

C-C motif chemokine receptor 1

0.531

0.769

0.39

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	22948
Gene Symbol:	CCT5

CCT5

chaperonin containing TCP1 subunit 5

0.663

0.462

1.00

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	9731
Gene Symbol:	CEP104

CEP104

centrosomal protein 104

0.670

0.423

1.2E-12

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	153241
Gene Symbol:	CEP120

CEP120

centrosomal protein 120

0.564

0.731

4.1E-15

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	95681
Gene Symbol:	CEP41

CEP41

centrosomal protein 41

0.636

0.500

3.6E-06

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	1073
Gene Symbol:	CFL2

CFL2

cofilin 2

0.659

0.500

6.4E-05

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	51142
Gene Symbol:	CHCHD2

CHCHD2

coiled-coil-helix-coiled-coil-helix domain containing 2

0.638

0.538

1.7E-07

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	55636
Gene Symbol:	CHD7

CHD7

chromodomain helicase DNA binding protein 7

0.441

0.846

1.00

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	25978
Gene Symbol:	CHMP2B

CHMP2B

charged multivesicular body protein 2B

0.543

0.731

4.6E-06

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	1146
Gene Symbol:	CHRNG

CHRNG

cholinergic receptor nicotinic gamma subunit

0.573

0.692

3.3E-19

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	84334
Gene Symbol:	COA8

COA8

cytochrome c oxidase assembly factor 8

0.682

0.538

2.1E-04

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	1280
Gene Symbol:	COL2A1

COL2A1

collagen type II alpha 1 chain

0.444

0.846

1.00

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	1297
Gene Symbol:	COL9A1

COL9A1

collagen type IX alpha 1 chain

0.566

0.731

3.1E-19

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None

Entrez Id:	1298
Gene Symbol:	COL9A2

COL9A2

collagen type IX alpha 2 chain

0.572

0.769

1.0E-08

CUI:	C4551915
Disease:	Gait Disturbance, CTCAE

Gait Disturbance, CTCAE

phenotype

0.100

None