DisGeNET - a database of gene-disease associations

Source: ORPHANET

Disease: Retinal Dystrophy, Early Onset Severe ×

Gene: LRAT ×

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:	9227
Gene Symbol:	LRAT

LRAT

lecithin retinol acyltransferase

0.608

0.654

2.8E-02

CUI:	C1858080
Disease:	Retinal Dystrophy, Early Onset Severe

Retinal Dystrophy, Early Onset Severe

disease

0.320

None

1.000

0

2001

2012