rs104894014
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Hyperinsulinemic hypoglycemia, familial, 3
0.800
GeneticVariation
UNIPROT
Heterogeneity in phenotype of hyperinsulinism caused by activating glucokinase mutations: a novel mutation and its functional characterization.
28247534
2017
rs104894014
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Hyperinsulinemic hypoglycemia, familial, 3
0.800
GeneticVariation
UNIPROT
Large islets, beta-cell proliferation, and a glucokinase mutation.
20375417
2010
rs104894014
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Hyperinsulinemic hypoglycemia, familial, 3
0.800
GeneticVariation
UNIPROT
Opposite clinical phenotypes of glucokinase disease: Description of a novel activating mutation and contiguous inactivating mutations in human glucokinase (GCK) gene.
19884385
2009
rs104894014
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Hyperinsulinemic hypoglycemia, familial, 3
0.800
GeneticVariation
UNIPROT
Biochemical basis of glucokinase activation and the regulation by glucokinase regulatory protein in naturally occurring mutations.
17082186
2006
rs104894014
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Hyperinsulinemic hypoglycemia, familial, 3
0.800
GeneticVariation
UNIPROT
Severe persistent hyperinsulinemic hypoglycemia due to a de novo glucokinase mutation.
15277402
2004
rs104894014
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Hyperinsulinemic hypoglycemia, familial, 3
0.800
GeneticVariation
UNIPROT
Insights into the biochemical and genetic basis of glucokinase activation from naturally occurring hypoglycemia mutations.
12941786
2003
rs104894014
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Hyperinsulinemic hypoglycemia, familial, 3
0.800
GeneticVariation
UNIPROT
The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapy.
11916951
2002
rs104894014
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Hyperinsulinemic hypoglycemia, familial, 3
0.800
GeneticVariation
UNIPROT
Familial hyperinsulinism caused by an activating glucokinase mutation.
9435328
1998
rs104894014
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Hyperinsulinemic hypoglycemia, familial, 3
A
0.800
CausalMutation
CLINVAR