|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
CausalMutation |
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
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
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
|
Muscle hypotonia
|
0.100 |
CausalMutation |
CLINVAR |
A selection system for human apoptosis inhibitors using yeast.
|
10509013 |
1999 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
CLINVAR |
A selection system for human apoptosis inhibitors using yeast.
|
10509013 |
1999 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
CLINVAR |
Accurate splicing of HDAC6 pre-mRNA requires SON.
|
25782155 |
2015 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
CausalMutation |
CLINVAR |
Accurate splicing of HDAC6 pre-mRNA requires SON.
|
25782155 |
2015 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
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
|
Muscle hypotonia
|
0.100 |
CausalMutation |
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
|
Muscle hypotonia
|
0.100 |
CausalMutation |
CLINVAR |
Characterising and predicting haploinsufficiency in the human genome.
|
20976243 |
2010 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
CLINVAR |
Characterising and predicting haploinsufficiency in the human genome.
|
20976243 |
2010 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
CausalMutation |
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
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
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
|
Muscle hypotonia
|
0.100 |
CausalMutation |
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
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
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
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
CLINVAR |
Diagnostic exome sequencing in persons with severe intellectual disability.
|
23033978 |
2012 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
CausalMutation |
CLINVAR |
Diagnostic exome sequencing in persons with severe intellectual disability.
|
23033978 |
2012 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
CLINVAR |
Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria.
|
22948023 |
2013 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
CausalMutation |
CLINVAR |
Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria.
|
22948023 |
2013 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
CausalMutation |
CLINVAR |
Genome sequencing identifies major causes of severe intellectual disability.
|
24896178 |
2014 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
CLINVAR |
Genome sequencing identifies major causes of severe intellectual disability.
|
24896178 |
2014 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
CLINVAR |
HDAC-6 interacts with and deacetylates tubulin and microtubules in vivo.
|
12606581 |
2003 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
CausalMutation |
CLINVAR |
HDAC-6 interacts with and deacetylates tubulin and microtubules in vivo.
|
12606581 |
2003 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
GeneticVariation |
CLINVAR |
Histone deacetylase 6 (HDAC6) is an independent deacetylase for alpha-tubulin.
|
19961433 |
2010 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
CausalMutation |
CLINVAR |
Histone deacetylase 6 (HDAC6) is an independent deacetylase for alpha-tubulin.
|
19961433 |
2010 |
|
| Entrez Id: |
6651 |
| Gene Symbol: |
SON |
SON
|
Muscle hypotonia
|
0.100 |
CausalMutation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |