DisGeNET - a database of gene-disease associations

Gene: NUDT2 ×

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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:	318
Gene Symbol:	NUDT2

NUDT2

CUI:	C0557874
Disease:	Global developmental delay

Global developmental delay

0.300

Biomarker

GENOMICS_ENGLAND

A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab children.

2018