DisGeNET - a database of gene-disease associations

Gene: SZT2 ×

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:	23334
Gene Symbol:	SZT2

SZT2

CUI:	C0424605
Disease:	Developmental delay (disorder)

Developmental delay (disorder)

0.320

Biomarker

GENOMICS_ENGLAND

An amino acid deletion inSZT2 in a family with non-syndromic intellectual disability.

2013