DisGeNET - a database of gene-disease associations

Source: INFERRED

Gene: ATP1A2 ×

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:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0003537
Disease:	Aphasia

Aphasia

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C1557375
Disease:	Blurred Vision, CTCAE

Blurred Vision, CTCAE

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0973461
Disease:	Dysphasia

Dysphasia

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0494475
Disease:	Tonic - clonic seizures

Tonic - clonic seizures

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0028738
Disease:	Nystagmus

Nystagmus

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0035334
Disease:	Retinitis Pigmentosa

Retinitis Pigmentosa

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0234985
Disease:	Mental deterioration

Mental deterioration

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0042571
Disease:	Vertigo

Vertigo

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0085583
Disease:	Choreoathetosis

Choreoathetosis

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0151611
Disease:	Electroencephalogram abnormal

Electroencephalogram abnormal

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0375206
Disease:	Hemiplegia/hemiparesis

Hemiplegia/hemiparesis

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0344232
Disease:	Blurred vision

Blurred vision

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0270685
Disease:	Cerebral calcification

Cerebral calcification

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0266464
Disease:	Polymicrogyria

Polymicrogyria

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C4554036
Disease:	Nystagmus, CTCAE 5.0

Nystagmus, CTCAE 5.0

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0003635
Disease:	Apraxias

Apraxias

group

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C2830004
Disease:	Somnolence

Somnolence

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0004134
Disease:	Ataxia

Ataxia

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C1963184
Disease:	Nystagmus, CTCAE 3.0

Nystagmus, CTCAE 3.0

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C1865332
Disease:	Transient unilateral blurring of vision

Transient unilateral blurring of vision

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0012569
Disease:	Diplopia

Diplopia

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0013144
Disease:	Drowsiness

Drowsiness

phenotype

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C0013362
Disease:	Dysarthria

Dysarthria

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C1863062
Disease:	Episodic quadriplegia

Episodic quadriplegia

disease

0.100

None

Entrez Id:	477
Gene Symbol:	ATP1A2

ATP1A2

ATPase Na+/K+ transporting subunit alpha 2

0.597

0.615

1.8E-04

CUI:	C1863061
Disease:	Episodic hemiplegia

Episodic hemiplegia

phenotype

0.100

None