Gene: CUL3 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR De novo genic mutations among a Chinese autism spectrum disorder cohort. 27824329

2016
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR De novo genic mutations among a Chinese autism spectrum disorder cohort. 27824329

2016
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders. 25969726

2015
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders. 25969726

2015
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Synaptic, transcriptional and chromatin genes disrupted in autism. 25363760

2014
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). 24266877

2014
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Kelch proteins: emerging roles in skeletal muscle development and diseases. 24959344

2014
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR Kelch proteins: emerging roles in skeletal muscle development and diseases. 24959344

2014
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR Synaptic, transcriptional and chromatin genes disrupted in autism. 25363760

2014
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). 24266877

2014
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Update on the Kelch-like (KLHL) gene family. 23676014

2013
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. 24267886

2013
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR De novo mutations in histone-modifying genes in congenital heart disease. 23665959

2013
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR De novo mutations in histone-modifying genes in congenital heart disease. 23665959

2013
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. 24267886

2013
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR Update on the Kelch-like (KLHL) gene family. 23676014

2013
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. 22495309

2012
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Rate of de novo mutations and the importance of father's age to disease risk. 22914163

2012
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities. 22266938

2012
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. 22495309

2012
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR Rate of de novo mutations and the importance of father's age to disease risk. 22914163

2012
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities. 22266938

2012
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR The cullin protein family. 21554755

2011
dbSNP: rs1553602498
rs1553602498
CUL3
A 0.700 CausalMutation CLINVAR The cullin protein family. 21554755

2011
dbSNP: rs1553521389
rs1553521389
CUL3
C 0.700 CausalMutation CLINVAR Structural assembly of cullin-RING ubiquitin ligase complexes. 20880695

2010