×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
27389779
2017
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
27389779
2017
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
28867767
2017
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
28867767
2017
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings.
26395437
2016
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings.
26395437
2016
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
BEFREE
Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings.
26395437
2016
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature.
26376624
2015
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
ARID1B-mediated disorders: Mutations and possible mechanisms.
25674384
2015
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
ARID1B-mediated disorders: Mutations and possible mechanisms.
25674384
2015
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature.
26376624
2015
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
Coffin-Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene.
24569609
2014
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
Coffin-Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene.
24569609
2014
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency.
24674232
2014
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
The ARID1B phenotype: what we have learned so far.
25169814
2014
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
The ARID1B phenotype: what we have learned so far.
25169814
2014
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
The contribution of de novo coding mutations to autism spectrum disorder.
25363768
2014
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
The contribution of de novo coding mutations to autism spectrum disorder.
25363768
2014
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency.
24674232
2014
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling.
23906836
2013
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling.
23906836
2013
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients.
23929686
2013
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
GeneticVariation
disease
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886
2013
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886
2013
×
Entrez Id:
57492
Gene Symbol:
ARID1B
ARID1B
0.110
CausalMutation
disease
CLINVAR
Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients.
23929686
2013