DisGeNET - a database of gene-disease associations

Source: MGD

Disease: DiGeorge Syndrome ×

Gene: CRKL ×

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:	1399
Gene Symbol:	CRKL

CRKL

CUI:	C0012236
Disease:	DiGeorge Syndrome

DiGeorge Syndrome

0.520

Biomarker

MGD

Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.

2001