Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Congenital Hyperinsulinism
|
disease |
0.700 |
None
|
1.000 |
0 |
0 |
2001 |
2019 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Maturity onset diabetes mellitus in young
|
disease |
0.660 |
strong
|
1.000 |
0 |
0 |
2009 |
2019 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Neonatal diabetes mellitus
|
disease |
0.500 |
None
|
0.988 |
0 |
2 |
2004 |
2019 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
DEND syndrome
|
disease |
0.490 |
strong
|
1.000 |
0 |
1 |
2007 |
2017 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Seizures
|
phenotype |
0.430 |
None
|
1.000 |
0 |
0 |
2007 |
2018 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Insulin Resistance
|
phenotype |
0.400 |
None
|
1.000 |
0 |
0 |
1997 |
1997 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Tonic - clonic seizures
|
disease |
0.400 |
None
|
1.000 |
0 |
0 |
2007 |
2007 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES
|
disease |
0.300 |
None
|
|
0 |
8 |
|
|
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Hyperinsulinemic hypoglycemia
|
disease |
0.200 |
None
|
1.000 |
0 |
0 |
2011 |
2016 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Diabetes Mellitus
|
group |
0.200 |
None
|
0.985 |
0 |
6 |
2003 |
2019 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Hypoglycemia
|
disease |
0.190 |
None
|
0.889 |
0 |
1 |
2003 |
2019 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Hyperinsulinism
|
disease |
0.190 |
None
|
1.000 |
0 |
1 |
2000 |
2017 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Global developmental delay
|
disease |
0.170 |
None
|
1.000 |
0 |
0 |
2005 |
2016 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Gestational Diabetes
|
phenotype |
0.150 |
None
|
0.800 |
0 |
0 |
2005 |
2013 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Transient neonatal diabetes mellitus
|
disease |
0.130 |
None
|
1.000 |
0 |
0 |
2008 |
2012 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Muscle Weakness
|
phenotype |
0.110 |
None
|
1.000 |
0 |
0 |
2004 |
2004 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Obesity
|
disease |
0.110 |
None
|
< 0.001 |
0 |
0 |
2014 |
2014 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Diarrhea
|
phenotype |
0.110 |
None
|
1.000 |
0 |
0 |
2005 |
2005 |
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Large for gestational age
|
phenotype |
0.100 |
None
|
|
0 |
0 |
|
|
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Contractures of the joints of the lower limbs
|
phenotype |
0.100 |
None
|
|
0 |
0 |
|
|
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Intellectual Disability
|
group |
0.100 |
None
|
|
0 |
0 |
|
|
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Microalbuminuria
|
phenotype |
0.100 |
None
|
|
0 |
0 |
|
|
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Prominent metopic ridge
|
phenotype |
0.100 |
None
|
|
0 |
0 |
|
|
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Reduced pancreatic beta cells
|
phenotype |
0.100 |
None
|
|
0 |
0 |
|
|
Entrez Id: |
3767 |
Gene Symbol: |
KCNJ11 |
KCNJ11
|
potassium inwardly rectifying channel subfamily J member 11
|
0.529 |
0.615 |
1.1E-02 |
Muscular hypotonia of the trunk
|
phenotype |
0.100 |
None
|
|
0 |
0 |
|
|