DisGeNET - a database of gene-disease associations

NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES, C4693405

Source: ALL

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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

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	57688
Gene Symbol:	ZSWIM6

ZSWIM6

0.400

Biomarker

disease

GENOMICS_ENGLAND

Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis.

2014

Entrez Id:	57688
Gene Symbol:	ZSWIM6

ZSWIM6

0.400

CausalMutation

disease

CLINVAR

Entrez Id:	57688
Gene Symbol:	ZSWIM6

ZSWIM6

0.400

Biomarker

disease

GENOMICS_ENGLAND