×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
0.600
GeneticVariation
CLINVAR
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
0.600
CausalMutation
CLINVAR
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism.
27848077
2017
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
28251352
2017
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Prevalence and architecture of de novo mutations in developmental disorders.
28135719
2017
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
Prevalence and architecture of de novo mutations in developmental disorders.
28135719
2017
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism.
27848077
2017
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
28251352
2017
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.
27479843
2016
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications.
26777411
2016
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications.
26777411
2016
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.
27479843
2016
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
The chromatin remodeller CHD8 is required for E2F-dependent transcription activation of S-phase genes.
24265227
2014
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Recurrent de novo mutations implicate novel genes underlying simplex autism risk.
25418537
2014
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
Recurrent de novo mutations implicate novel genes underlying simplex autism risk.
25418537
2014
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
The chromatin remodeller CHD8 is required for E2F-dependent transcription activation of S-phase genes.
24265227
2014
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886
2013
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Response to comment on: Draznin et al. Pathways to quality inpatient management of hyperglycemia and diabetes: a call to action. Diabetes Care 2013;36:1807-1814.
24265389
2013
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886
2013
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
Response to comment on: Draznin et al. Pathways to quality inpatient management of hyperglycemia and diabetes: a call to action. Diabetes Care 2013;36:1807-1814.
24265389
2013
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
TRIP12 and UBR5 suppress spreading of chromatin ubiquitylation at damaged chromosomes.
22884692
2012
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
De novo gene disruptions in children on the autistic spectrum.
22542183
2012
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism.
22511880
2012
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
De novo gene disruptions in children on the autistic spectrum.
22542183
2012
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Dysmorphic features
0.100
CausalMutation
CLINVAR
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism.
22511880
2012