×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
UNIPROT
RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients.
27736983
2016
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
UNIPROT
Biochemical and Functional Characterization of RNF213 (Mysterin) R4810K, a Susceptibility Mutation of Moyamoya Disease, in Angiogenesis In Vitro and In Vivo.
26126547
2015
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
UNIPROT
Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan.
25956231
2015
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
UNIPROT
Atypical presentation of moyamoya disease in an infant with a de novo RNF213 variant.
26198278
2015
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
UNIPROT
RNF213 rare variants in an ethnically diverse population with Moyamoya disease.
25278557
2014
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
CLINVAR
RNF213 rare variants in an ethnically diverse population with Moyamoya disease.
25278557
2014
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
UNIPROT
The moyamoya disease susceptibility variant RNF213 R4810K (rs112735431) induces genomic instability by mitotic abnormality.
23994138
2013
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
UNIPROT
Molecular analysis of RNF213 gene for moyamoya disease in the Chinese Han population.
23110205
2012
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
UNIPROT
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.
21048783
2011
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
GeneticVariation
disease
UNIPROT
Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development.
21799892
2011
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
SusceptibilityMutation
disease
CLINVAR
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
CausalMutation
disease
CLINVAR
×
Entrez Id:
57674
Gene Symbol:
RNF213
RNF213
0.600
Biomarker
disease
CTD_human
RNF213-AS1
0.100
GeneticVariation
disease
CLINVAR
RNF213 rare variants in an ethnically diverse population with Moyamoya disease.
25278557
2014
RNF213-AS1
0.100
SusceptibilityMutation
disease
CLINVAR
RNF213-AS1
0.100
CausalMutation
disease
CLINVAR