Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation CLINVAR Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report. 27540107

2016
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation 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
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation 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
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation CLINVAR De novo mutations revealed by whole-exome sequencing are strongly associated with autism. 22495306

2012
Entrez Id: 63925
Gene Symbol: ZNF335
ZNF335
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation CLINVAR Identification and characterization of a novel nuclear protein complex involved in nuclear hormone receptor-mediated gene regulation. 19131338

2009