Gene: CRKL ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1399
Gene Symbol: CRKL
CRKL 		0.020 Biomarker disease BEFREE Sequencing of CRKL, implicated in renal tract malformations in DiGeorge syndrome critical region at 22q11, in 89 individuals with BEEC lacking 22q11 duplications revealed no pathogenic variants. 30628148 2019
Entrez Id: 1399
Gene Symbol: CRKL
CRKL 		0.020 GeneticVariation disease BEFREE Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome. 11242111 2001