Gene: ZMYND11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10771
Gene Symbol: ZMYND11
ZMYND11 		0.100 CausalMutation phenotype CLINVAR A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability. 25281490 2015
Entrez Id: 10771
Gene Symbol: ZMYND11
ZMYND11 		0.100 CausalMutation phenotype CLINVAR ZMYND11 links histone H3.3K36me3 to transcription elongation and tumour suppression. 24590075 2014
Entrez Id: 10771
Gene Symbol: ZMYND11
ZMYND11 		0.100 CausalMutation phenotype CLINVAR Refining analyses of copy number variation identifies specific genes associated with developmental delay. 25217958 2014
Entrez Id: 10771
Gene Symbol: ZMYND11
ZMYND11 		0.100 CausalMutation phenotype CLINVAR ZMYND11: an H3.3-specific reader of H3K36me3. 24963723 2014
Entrez Id: 10771
Gene Symbol: ZMYND11
ZMYND11 		0.100 CausalMutation phenotype CLINVAR Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. 24267886 2013
Entrez Id: 10771
Gene Symbol: ZMYND11
ZMYND11 		0.100 CausalMutation phenotype CLINVAR Structural and functional analysis of the DEAF-1 and BS69 MYND domains. 23372760 2013
Entrez Id: 10771
Gene Symbol: ZMYND11
ZMYND11 		0.100 CausalMutation phenotype CLINVAR Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenetic characterization. 22847950 2012
Entrez Id: 10771
Gene Symbol: ZMYND11
ZMYND11 		0.100 CausalMutation phenotype CLINVAR New insights into BS69 functions. 16565076 2006