×
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
×
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
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
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
Are there distinctive sleep problems in Angelman syndrome?
17765640
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
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
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
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
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
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
Mutation Update for UBE3A variants in Angelman syndrome.
25212744
2014
×
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