rs1057517955
|
KDM5C;MIR6894
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.
|
27421841 |
2016 |
rs1556836399
|
KDM5C;MIR6895
|
Overgrowth
|
A |
0.700 |
CausalMutation |
CLINVAR |
Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.
|
27421841 |
2016 |
rs1556836399
|
KDM5C;MIR6895
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.
|
27421841 |
2016 |
rs1556837420
|
KDM5C;MIR6895
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.
|
27421841 |
2016 |
rs1556837420
|
KDM5C;MIR6895
|
Movement Disorders
|
A |
0.700 |
CausalMutation |
CLINVAR |
Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.
|
27421841 |
2016 |
rs199422235
|
Entrez Id: |
8242 |
Gene Symbol: |
KDM5C |
KDM5C
|
Dysmorphic features
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.
|
27421841 |
2016 |
rs1057517955
|
KDM5C;MIR6894
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
|
26919706 |
2016 |
rs1556836399
|
KDM5C;MIR6895
|
Overgrowth
|
A |
0.700 |
CausalMutation |
CLINVAR |
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
|
26919706 |
2016 |
rs1556836399
|
KDM5C;MIR6895
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
|
26919706 |
2016 |
rs1556837420
|
KDM5C;MIR6895
|
Movement Disorders
|
A |
0.700 |
CausalMutation |
CLINVAR |
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
|
26919706 |
2016 |
rs1556837420
|
KDM5C;MIR6895
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
|
26919706 |
2016 |
rs199422235
|
Entrez Id: |
8242 |
Gene Symbol: |
KDM5C |
KDM5C
|
Dysmorphic features
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
|
26919706 |
2016 |
rs1057517955
|
KDM5C;MIR6894
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.
|
25666439 |
2015 |
rs1556836399
|
KDM5C;MIR6895
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.
|
25666439 |
2015 |
rs1556836399
|
KDM5C;MIR6895
|
Overgrowth
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.
|
25666439 |
2015 |
rs1556837420
|
KDM5C;MIR6895
|
Movement Disorders
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.
|
25666439 |
2015 |
rs1556837420
|
KDM5C;MIR6895
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.
|
25666439 |
2015 |
rs1569285562
|
Entrez Id: |
8242 |
Gene Symbol: |
KDM5C |
KDM5C
|
Spastic Paraplegia
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.
|
25666439 |
2015 |
rs199422235
|
Entrez Id: |
8242 |
Gene Symbol: |
KDM5C |
KDM5C
|
Dysmorphic features
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.
|
25666439 |
2015 |
rs1057517955
|
KDM5C;MIR6894
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.
|
24583395 |
2014 |
rs1556836399
|
KDM5C;MIR6895
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.
|
24583395 |
2014 |
rs1556836399
|
KDM5C;MIR6895
|
Overgrowth
|
A |
0.700 |
CausalMutation |
CLINVAR |
KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.
|
24583395 |
2014 |
rs1556837420
|
KDM5C;MIR6895
|
Movement Disorders
|
A |
0.700 |
CausalMutation |
CLINVAR |
KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.
|
24583395 |
2014 |
rs1556837420
|
KDM5C;MIR6895
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.
|
24583395 |
2014 |
rs199422235
|
Entrez Id: |
8242 |
Gene Symbol: |
KDM5C |
KDM5C
|
Dysmorphic features
|
G |
0.700 |
GeneticVariation |
CLINVAR |
KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.
|
24583395 |
2014 |