Gene: CCDC22 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 28952
Gene Symbol: CCDC22
CCDC22 		0.510 GeneticVariation disease BEFREE We identified a variant in CCDC22 gene as the cause of an X-linked phenotype similar to RSS/3C syndrome in the family described here. 24916641 2015
Entrez Id: 28952
Gene Symbol: CCDC22
CCDC22 		0.510 GermlineCausalMutation disease ORPHANET We identified a variant in CCDC22 gene as the cause of an X-linked phenotype similar to RSS/3C syndrome in the family described here. 24916641 2015
Entrez Id: 28952
Gene Symbol: CCDC22
CCDC22 		0.510 Biomarker disease CTD_human