Gene: SNHG14 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 CausalMutation group 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 		0.100 GeneticVariation group 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 		0.100 GeneticVariation group CLINVAR The neurobehavioral and molecular phenotype of Angelman Syndrome. 26219744 2015
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 CausalMutation group CLINVAR The neurobehavioral and molecular phenotype of Angelman Syndrome. 26219744 2015
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 GeneticVariation group CLINVAR Mutation Update for UBE3A variants in Angelman syndrome. 25212744 2014
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 CausalMutation group CLINVAR Angelman syndrome: review of clinical and molecular aspects. 24876791 2014
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 GeneticVariation group CLINVAR Angelman syndrome: review of clinical and molecular aspects. 24876791 2014
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 CausalMutation group CLINVAR Mutation Update for UBE3A variants in Angelman syndrome. 25212744 2014
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 GeneticVariation group CLINVAR Molecular and Clinical Aspects of Angelman Syndrome. 22670133 2012
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 CausalMutation group CLINVAR Molecular and Clinical Aspects of Angelman Syndrome. 22670133 2012
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 CausalMutation group 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 		0.100 GeneticVariation group 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 		0.100 CausalMutation group CLINVAR Are there distinctive sleep problems in Angelman syndrome? 17765640 2008
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 GeneticVariation group 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 		0.100 CausalMutation group 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 		0.100 GeneticVariation group CLINVAR Are there distinctive sleep problems in Angelman syndrome? 17765640 2008
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 CausalMutation group CLINVAR Angelman syndrome 2005: updated consensus for diagnostic criteria. 16470747 2006
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 GeneticVariation group CLINVAR Angelman syndrome 2005: updated consensus for diagnostic criteria. 16470747 2006
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 CausalMutation group 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 		0.100 GeneticVariation group 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 		0.100 CausalMutation group CLINVAR UBE3A/E6-AP mutations cause Angelman syndrome. 8988171 1997
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 GeneticVariation group CLINVAR UBE3A/E6-AP mutations cause Angelman syndrome. 8988171 1997
Entrez Id: 104472715
Gene Symbol: SNHG14
SNHG14 		0.100 CausalMutation group 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 		0.100 GeneticVariation group CLINVAR Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting. 2309781 1990