×
Entrez Id: 55786
Gene Symbol: ZNF415
ZNF415
0.010
GeneticVariation
group
BEFREE
A truncated PACT protein resulting from a frameshift mutation reported in movement disorder DYT16 triggers caspase activation and apoptosis.
31246344 2019
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
GeneticVariation
group
CLINVAR
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
22495306 2012
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
GeneticVariation
group
CLINVAR
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.
26795593 2016
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
GeneticVariation
group
CLINVAR
Identification and characterization of a novel nuclear protein complex involved in nuclear hormone receptor-mediated gene regulation.
19131338 2009
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
GeneticVariation
group
CLINVAR
Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report.
27540107 2016
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
CausalMutation
group
CLINVAR
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
22495306 2012
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
CausalMutation
group
CLINVAR
Identification and characterization of a novel nuclear protein complex involved in nuclear hormone receptor-mediated gene regulation.
19131338 2009
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
GeneticVariation
group
CLINVAR
Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation.
23178126 2012
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
CausalMutation
group
CLINVAR
Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation.
23178126 2012
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
CausalMutation
group
CLINVAR
Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report.
27540107 2016
×
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
0.100
CausalMutation
group
CLINVAR
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.
26795593 2016
×
Entrez Id: 23503
Gene Symbol: ZFYVE26
ZFYVE26
0.100
GeneticVariation
group
CLINVAR
Exome sequencing in undiagnosed inherited and sporadic ataxias.
25497598 2015
×
Entrez Id: 23503
Gene Symbol: ZFYVE26
ZFYVE26
0.100
GeneticVariation
group
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886 2013
×
Entrez Id: 55906
Gene Symbol: ZC4H2
ZC4H2
0.100
Biomarker
group
HPO
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43-q44.
21934713 2012
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
Transcription factor haploinsufficiency: when half a loaf is not enough.
11854316 2002
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
Haploinsufficiency of ZNF238 is associated with corpus callosum abnormalities in 1q44 deletions.
23494996 2013
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
Rp58 is essential for the growth and patterning of the cerebellum and for glutamatergic and GABAergic neuron development.
22513377 2012
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
A systems approach reveals that the myogenesis genome network is regulated by the transcriptional repressor RP58.
20059953 2009
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.
20672375 2010
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
The transcriptional repressor RP58 is crucial for cell-division patterning and neuronal survival in the developing cortex.
19409883 2009
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.
17668379 2007
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene.
20382278 2010
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
Dnmt3a binds deacetylases and is recruited by a sequence-specific repressor to silence transcription.
11350943 2001
×
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
0.100
GeneticVariation
group
CLINVAR
High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.
21800092 2012