×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Organization and conservation of the GART/SON/DONSON locus in mouse and human genomes.
10950926
2000
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
25590979
2015
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Son is essential for nuclear speckle organization and cell cycle progression.
20053686
2010
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Genome sequencing identifies major causes of severe intellectual disability.
24896178
2014
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortex.
23416452
2013
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Accurate splicing of HDAC6 pre-mRNA requires SON.
25782155
2015
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.
23603762
2013
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive.
27545676
2016
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene.
23595291
2013
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
SON connects the splicing-regulatory network with pluripotency in human embryonic stem cells.
24013217
2013
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Molecular cloning of Fyn-associated molecules in the mouse central nervous system.
9185665
1997
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
A selection system for human apoptosis inhibitors using yeast.
10509013
1999
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria.
22948023
2013
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
SON controls cell-cycle progression by coordinated regulation of RNA splicing.
21504830
2011
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Diagnostic exome sequencing in persons with severe intellectual disability.
23033978
2012
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Characterising and predicting haploinsufficiency in the human genome.
20976243
2010
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
A genome-wide in situ hybridization map of RNA-binding proteins reveals anatomically restricted expression in the developing mouse brain.
16033648
2005
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
SON is a spliceosome-associated factor required for mitotic progression.
20581448
2010
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Transcription repression of human hepatitis B virus genes by negative regulatory element-binding protein/SON.
11306577
2001
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.
23001566
2012
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
[Identification of a protein product of a novel human gene SON and the biological effect upon administering a changed form of this gene into mammalian cells].
1944255
1991
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
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
0.100
CausalMutation
group
CLINVAR
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia.
23424103
2013
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
[Decoding of the primary structure of the son3 region in human genome: identification of a new protein with unusual structure and homology with DNA-binding proteins].
3054499
1988
×
Entrez Id:
6651
Gene Symbol:
SON
SON
0.100
CausalMutation
group
CLINVAR
Histone deacetylase 6 (HDAC6) is an independent deacetylase for alpha-tubulin.
19961433
2010