DisGeNET - a database of gene-disease associations

Gene: OTX2 ×

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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:	5015
Gene Symbol:	OTX2

OTX2

CUI:	C0015923
Disease:	Fetal Alcohol Syndrome

Fetal Alcohol Syndrome

0.300

Biomarker

PSYGENET

Of these, four (Pten, Nmnat1, Slitrk2 and Otx2) were viewed as being crucial in the context of FASDs given their roles in the brain.

2013