Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR 15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes. 25884337

2015
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR 15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes. 25884337

2015
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR The neurobehavioral and molecular phenotype of Angelman Syndrome. 26219744

2015
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR The neurobehavioral and molecular phenotype of Angelman Syndrome. 26219744

2015
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Mutation Update for UBE3A variants in Angelman syndrome. 25212744

2014
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Angelman syndrome: review of clinical and molecular aspects. 24876791

2014
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Angelman syndrome: review of clinical and molecular aspects. 24876791

2014
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Mutation Update for UBE3A variants in Angelman syndrome. 25212744

2014
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Molecular and Clinical Aspects of Angelman Syndrome. 22670133

2012
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Molecular and Clinical Aspects of Angelman Syndrome. 22670133

2012
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Novel UBE3A mutations causing Angelman syndrome: different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions. 19213023

2009
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Novel UBE3A mutations causing Angelman syndrome: different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions. 19213023

2009
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Are there distinctive sleep problems in Angelman syndrome? 17765640

2008
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology. 17940072

2008
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology. 17940072

2008
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Are there distinctive sleep problems in Angelman syndrome? 17765640

2008
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Angelman syndrome 2005: updated consensus for diagnostic criteria. 16470747

2006
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Angelman syndrome 2005: updated consensus for diagnostic criteria. 16470747

2006
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Biochemical analysis of Angelman syndrome-associated mutations in the E3 ubiquitin ligase E6-associated protein. 15263005

2004
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Biochemical analysis of Angelman syndrome-associated mutations in the E3 ubiquitin ligase E6-associated protein. 15263005

2004
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR UBE3A/E6-AP mutations cause Angelman syndrome. 8988171

1997
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR UBE3A/E6-AP mutations cause Angelman syndrome. 8988171

1997
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting. 2309781

1990
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting. 2309781

1990