Gene: ZMYND11

Alternate names for this Gene: BRAM1|BS69|MRD30

Gene Summary: The protein encoded by this gene was first identified by its ability to bind the adenovirus E1A protein. The protein localizes to the nucleus. It functions as a transcriptional repressor, and expression of E1A inhibits this repression. Alternatively spliced transcript variants encoding different isoforms have been identified.

Gene is located in Chromosome: 10

Location in Chromosome : 10p15.3

Description of this Gene: zinc finger MYND-type containing 11

Type of Gene: protein-coding

rs797044854 in ZMYND11 gene and Dysmorphic features PMID 24590075 2014 ZMYND11 links histone H3.3K36me3 to transcription elongation and tumour suppression.

PMID 25281490 2015 A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability.

PMID 24963723 2014 ZMYND11: an H3.3-specific reader of H3K36me3.

PMID 23372760 2013 Structural and functional analysis of the DEAF-1 and BS69 MYND domains.

PMID 25217958 2014 Refining analyses of copy number variation identifies specific genes associated with developmental delay.

PMID 24267886 2013 Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.

PMID 16565076 2006 New insights into BS69 functions.

PMID 22847950 2012 Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenetic characterization.

rs797044854 in ZMYND11 gene and Multiple congenital anomalies PMID 24590075 2014 ZMYND11 links histone H3.3K36me3 to transcription elongation and tumour suppression.

PMID 24963723 2014 ZMYND11: an H3.3-specific reader of H3K36me3.

PMID 25281490 2015 A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability.

PMID 25217958 2014 Refining analyses of copy number variation identifies specific genes associated with developmental delay.

PMID 24267886 2013 Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.

PMID 22847950 2012 Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenetic characterization.

PMID 23372760 2013 Structural and functional analysis of the DEAF-1 and BS69 MYND domains.

PMID 16565076 2006 New insights into BS69 functions.

rs797044854 in ZMYND11 gene and Muscle hypotonia PMID 25217958 2014 Refining analyses of copy number variation identifies specific genes associated with developmental delay.

PMID 25281490 2015 A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability.

PMID 24963723 2014 ZMYND11: an H3.3-specific reader of H3K36me3.

PMID 23372760 2013 Structural and functional analysis of the DEAF-1 and BS69 MYND domains.

PMID 22847950 2012 Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenetic characterization.

PMID 16565076 2006 New insights into BS69 functions.

PMID 24590075 2014 ZMYND11 links histone H3.3K36me3 to transcription elongation and tumour suppression.

PMID 24267886 2013 Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.