DisGeNET - a database of gene-disease associations

Source: INFERRED

Disease: Optic Atrophy ×

Gene: ISCA2 ×

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

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	122961
Gene Symbol:	ISCA2

ISCA2

CUI:	C0029124
Disease:	Optic Atrophy

Optic Atrophy

0.100

GeneticVariation

CLINVAR

Entrez Id:	122961
Gene Symbol:	ISCA2

ISCA2

CUI:	C0029124
Disease:	Optic Atrophy

Optic Atrophy

0.100

Biomarker

HPO