ZNF335, zinc finger protein 335, 63925

N. diseases: 45; N. variants: 17
Disease: Movement Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1350201776
rs1350201776
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy. 26795593 2016
dbSNP: rs1350201776
rs1350201776
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report. 27540107 2016
dbSNP: rs1350201776
rs1350201776
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation. 23178126 2012
dbSNP: rs1350201776
rs1350201776
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR De novo mutations revealed by whole-exome sequencing are strongly associated with autism. 22495306 2012
dbSNP: rs1350201776
rs1350201776
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Identification and characterization of a novel nuclear protein complex involved in nuclear hormone receptor-mediated gene regulation. 19131338 2009