GCG, glucagon, 2641

N. diseases: 441; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1037733674
rs1037733674
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE Our results show that the Gly40Ser mutation in the glucagon receptor gene is not associated with type 2 diabetes in a Brazilian population. 11961492 2002
dbSNP: rs1037733674
rs1037733674
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE Our results demonstrate a strong genetic heterogeneity among the ethnic group and suggest that the Gly40Ser mutation of the glucagon receptor gene plays little role, if any, in the pathogenesis of type 2 diabetes and essential hypertension in the Taiwanese population. 10090412 1999
dbSNP: rs1037733674
rs1037733674
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE In conclusion, our results indicate that the Gly40Ser variation is not associated with NIDDM in the Sardinian population and that its frequency varies in different parts of Sardinia. 9028723 1997
dbSNP: rs1037733674
rs1037733674
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE We have previously reported that a single heterozygous missense mutation in exon 2 of the glucagon receptor gene, which changes a glycine to a serine (Gly40Ser), is associated with NIDDM in a French population. 8635644 1996
dbSNP: rs1037733674
rs1037733674
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0085580
Disease:
Essential Hypertension
0.020 GeneticVariation BEFREE Our results demonstrate a strong genetic heterogeneity among the ethnic group and suggest that the Gly40Ser mutation of the glucagon receptor gene plays little role, if any, in the pathogenesis of type 2 diabetes and essential hypertension in the Taiwanese population. 10090412 1999
dbSNP: rs1037733674
rs1037733674
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0085580
Disease:
Essential Hypertension
0.020 GeneticVariation BEFREE 1.Previous glucagon receptor gene (GCGR) studies have shown a Gly40Ser mutation to be more prevalent in essential hypertension and to affect glucagon binding affinity to its receptor. 9673441 1998
dbSNP: rs980303898
rs980303898
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0346647
Disease:
Malignant neoplasm of pancreas
0.010 GeneticVariation BEFREE K-ras<sup>LSL-G12D/+</sup>:: p53<sup>LSL-R172H/+</sup>:: Pdx-1-Cre (KPC) mice are an established model of pancreatic cancer that specifically express mutants of both K-ras and p53 in the pancreas by using Pdx-1-Cre. 28971839 2018
dbSNP: rs980303898
rs980303898
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0235974
Disease:
Pancreatic carcinoma
0.010 GeneticVariation BEFREE K-ras<sup>LSL-G12D/+</sup>:: p53<sup>LSL-R172H/+</sup>:: Pdx-1-Cre (KPC) mice are an established model of pancreatic cancer that specifically express mutants of both K-ras and p53 in the pancreas by using Pdx-1-Cre. 28971839 2018
dbSNP: rs749317102
rs749317102
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0021670
Disease:
insulinoma
0.010 GeneticVariation BEFREE The clinical study was combined with in vitro studies of the synthesis and secretion of p.R46Q-insulin in rat INS-1 insulinoma cells. 28478482 2017
dbSNP: rs183433761
rs183433761
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0238033
Disease:
Carcinoma of Male Breast
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs183433761
rs183433761
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs183433761
rs183433761
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0242787
Disease:
Malignant neoplasm of male breast
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs183433761
rs183433761
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs183433761
rs183433761
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs770254254
rs770254254
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0025322
Disease:
Premature Menopause
0.010 GeneticVariation BEFREE WNT4 (c.99G>A, p.Ser33Ser) was not associated with POF pathology. 22951804 2012
dbSNP: rs770254254
rs770254254
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0085215
Disease:
Ovarian Failure, Premature
0.010 GeneticVariation BEFREE WNT4 (c.99G>A, p.Ser33Ser) was not associated with POF pathology. 22951804 2012
dbSNP: rs980303898
rs980303898
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0149521
Disease:
Pancreatitis, Chronic
0.010 GeneticVariation BEFREE In the pancreata of Pdx1-Cre; LSL-Kras(G12D) mice, exendin-4 led to acceleration of the disruption of exocrine architecture and chronic pancreatitis with mucinous metaplasia and increased formation of murine PanIN lesions. 22266668 2012
dbSNP: rs980303898
rs980303898
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C1301034
Disease:
Pancreatic intraepithelial neoplasia
0.010 GeneticVariation BEFREE In the pancreata of Pdx1-Cre; LSL-Kras(G12D) mice, exendin-4 led to acceleration of the disruption of exocrine architecture and chronic pancreatitis with mucinous metaplasia and increased formation of murine PanIN lesions. 22266668 2012
dbSNP: rs766216371
rs766216371
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
0.010 GeneticVariation BEFREE Permanent neonatal diabetes mellitus caused by a novel homozygous (T168A) glucokinase (GCK) mutation: initial response to oral sulphonylurea therapy. 18571549 2008
dbSNP: rs1037733674
rs1037733674
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011847
Disease:
Diabetes
0.010 GeneticVariation BEFREE Patients with diabetes and carriers of Gly40Ser showed basal C-peptide levels significantly lower than noncarriers (0.70 ng/mL versus 1.50 ng/mL, p = 0.008). 11961492 2002
dbSNP: rs1037733674
rs1037733674
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011849
Disease:
Diabetes Mellitus
0.010 GeneticVariation BEFREE Patients with diabetes and carriers of Gly40Ser showed basal C-peptide levels significantly lower than noncarriers (0.70 ng/mL versus 1.50 ng/mL, p = 0.008). 11961492 2002
dbSNP: rs1303328174
rs1303328174
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.010 GeneticVariation BEFREE The nucleotide substitutions in exon 4 in the patient with type 1 diabetes and that with fibrocalculous pancreatopathy occurred at codons 103 and 84 while that in exon 5 in the patient with type 1 diabetes occurred at codon 141, changing the codons from CAT to CAC, GTG to GCG, and ACT to AAT and resulting in H103H silent, V84A and T141N missense mutations, respectively. 11796176 2002
dbSNP: rs150179526
rs150179526
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011847
Disease:
Diabetes
0.010 GeneticVariation BEFREE V125I mutation co-segregated in those 2 initial families, but further association studies showed that this mutation was not associated with diabetes or early age at diagnosis of the disease. 11773861 2002
dbSNP: rs150179526
rs150179526
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011849
Disease:
Diabetes Mellitus
0.010 GeneticVariation BEFREE V125I mutation co-segregated in those 2 initial families, but further association studies showed that this mutation was not associated with diabetes or early age at diagnosis of the disease. 11773861 2002
dbSNP: rs375960284
rs375960284
Entrez Id: 2641;101929532
Gene Symbol: GCG;LOC101929532
GCG;LOC101929532
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.010 GeneticVariation BEFREE The nucleotide substitutions in exon 4 in the patient with type 1 diabetes and that with fibrocalculous pancreatopathy occurred at codons 103 and 84 while that in exon 5 in the patient with type 1 diabetes occurred at codon 141, changing the codons from CAT to CAC, GTG to GCG, and ACT to AAT and resulting in H103H silent, V84A and T141N missense mutations, respectively. 11796176 2002