×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
GeneticVariation
disease
CLINVAR
INS-gene mutations: from genetics and beta cell biology to clinical disease.
25542748
2015
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
GeneticVariation
disease
UNIPROT
Structural and functional study of the GlnB22-insulin mutant responsible for maturity-onset diabetes of the young.
25423173
2014
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
GeneticVariation
disease
CLINVAR
Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).
20226046
2010
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
GeneticVariation
disease
UNIPROT
Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).
20226046
2010
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
GeneticVariation
disease
UNIPROT
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.
18192540
2008
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
GeneticVariation
disease
CLINVAR
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.
18192540
2008
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
GeneticVariation
disease
UNIPROT
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
18162506
2008
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
GeneticVariation
disease
CLINVAR
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
18162506
2008
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
Biomarker
disease
GENOMICS_ENGLAND
Insulin gene mutations as a cause of permanent neonatal diabetes.
17855560
2007
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
GeneticVariation
disease
CLINVAR
Insulin gene mutations as a cause of permanent neonatal diabetes.
17855560
2007
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
CausalMutation
disease
CLINVAR
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.700
Biomarker
disease
CTD_human