Gene: DCDC2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.410 CausalMutation disease CLINVAR A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation. 25601850 2015
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.410 Biomarker disease CLINGEN A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation. 25601850 2015
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.410 Biomarker disease CLINGEN Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability. 25130614 2014
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.410 Biomarker disease CLINGEN Exploring the transcriptome of ciliated cells using in silico dissection of human tissues. 22558177 2012
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.410 GeneticVariation disease BEFREE DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss. 21816241 2012