×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
Biomarker
phenotype
BEFREE
Original articles on ZTTK syndrome published up to November 20l8 were identified from PubMed, Human Gene Mutation Database, Online Mendelian Inheritance in Man, China National Knowledge Infrastructure, and WanFang databases using the keywords "ZTTK syndrome " and "SON ".
31557424
2019
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
GermlineCausalMutation
phenotype
ORPHANET
Establishing SON in 21q22.11 as a cause a new syndromic form of intellectual disability: Possible contribution to Braddock-Carey syndrome phenotype.
27256762
2016
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
GeneticVariation
phenotype
UNIPROT
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome.
27545680
2016
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
GeneticVariation
phenotype
UNIPROT
Establishing SON in 21q22.11 as a cause a new syndromic form of intellectual disability: Possible contribution to Braddock-Carey syndrome phenotype.
27256762
2016
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
GermlineCausalMutation
phenotype
ORPHANET
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome.
27545680
2016
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
GeneticVariation
phenotype
UNIPROT
De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive.
27545676
2016
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
GermlineCausalMutation
phenotype
ORPHANET
De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive.
27545676
2016
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
Biomarker
phenotype
GENOMICS_ENGLAND
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome.
27545680
2016
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
GeneticVariation
phenotype
UNIPROT
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
25590979
2015
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
GeneticVariation
phenotype
CLINVAR
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
Biomarker
phenotype
GENOMICS_ENGLAND
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.710
Biomarker
phenotype
CTD_human