rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia.
|
29130632 |
2018 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Biallelic loss-of-function variants in DOCK3 cause muscle hypotonia, ataxia, and intellectual disability.
|
28195318 |
2017 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.
|
28139846 |
2017 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia.
|
25599672 |
2015 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
UniProt: a hub for protein information.
|
25348405 |
2015 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A draft map of the human proteome.
|
24870542 |
2014 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Genome sequencing identifies major causes of severe intellectual disability.
|
24896178 |
2014 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Dock GEFs and their therapeutic potential: neuroprotection and axon regeneration.
|
25016980 |
2014 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Dock3 induces axonal outgrowth by stimulating membrane recruitment of the WAVE complex.
|
20368433 |
2010 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Loss of modifier of cell adhesion reveals a pathway leading to axonal degeneration.
|
19129390 |
2009 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
BDNF and memory formation and storage.
|
17911219 |
2008 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Neurotrophin receptor homolog (NRH1) proteins regulate mesoderm formation and apoptosis during early Xenopus development.
|
17055478 |
2006 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation.
|
17046689 |
2006 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
TrkB has a cell-autonomous role in the establishment of hippocampal Schaffer collateral synapses.
|
15829629 |
2005 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Nonsense-mediated decay approaches the clinic.
|
15284851 |
2004 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A de novo mutation affecting human TrkB associated with severe obesity and developmental delay.
|
15494731 |
2004 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Regulation of dendritic spine motility and stability by Rac1 and Rho kinase: evidence for two forms of spine motility.
|
15234347 |
2004 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype.
|
14569117 |
2003 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Signalling mechanisms mediating neuronal responses to guidance cues.
|
14682358 |
2003 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A novel pericentric inversion of chromosome 3 cosegregates with a developmental-behavioural phenotype.
|
12566533 |
2003 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identification of an evolutionarily conserved superfamily of DOCK180-related proteins with guanine nucleotide exchange activity.
|
12432077 |
2002 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Isolation and characterization of novel presenilin binding protein.
|
10854253 |
2000 |
rs1553749681
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Small GTPases Rac and Rho in the maintenance of dendritic spines and branches in hippocampal pyramidal neurons.
|
10884317 |
2000 |
rs1560212751
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1560414254
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|