DisGeNET - a database of gene-disease associations

Gene: MID2 ×

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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:	11043
Gene Symbol:	MID2

MID2

CUI:	C2931498
Disease:	Mental Retardation, X-Linked 1

Mental Retardation, X-Linked 1

0.300

GermlineCausalMutation

ORPHANET

Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India.

2014