HK2, hexokinase 2, 3099

N. diseases: 152; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation disease BEFREE Genetic variation in hexokinase II could underlie insulin resistance in peripheral tissues and cause non-insulin-dependent diabetes mellitus. 8250948 1993
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation disease BEFREE Mutations in the gene encoding hexokinase II which catalyzes a key step in glycolysis could contribute to the development of peripheral insulin resistance and lead to non-insulin-dependent diabetes mellitus. 7999069 1994
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation disease BEFREE Therefore, mutations in the HK2 gene could contribute to skeletal muscle insulin resistance in NIDDM. 8786021 1995
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation disease BEFREE We conclude that mutations of the HKII gene are not a major etiological factor for NIDDM in the Finnish population. 7883120 1995
Diabetes Mellitus, Non-Insulin-Dependent
0.100 AlteredExpression disease BEFREE HKII mRNA, HKII immunoreactive protein level, and HKII activity were significantly decreased in NIDDM patients (P < 0.0001, P = 0.03, and P = 0.02, respectively) together with significantly decreased glycogen synthase mRNA level and total glycogen synthase activity (P = 0.02 and P = 0.02, respectively). 8675629 1995
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation disease BEFREE In conclusion, polymorphisms in the hexokinase II gene are not associated with the risk of NIDDM or insulin resistance in the Finnish population. 7489847 1995
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation disease BEFREE Since reduced insulin-stimulated glucose uptake and reduced glucose-6-phosphate content in muscle have been demonstrated in pre-non-insulin-dependent diabetes mellitus (pre-NIDDM) and NIDDM subjects, we have examined the coding region of the HKII gene in NIDDM patients to determine whether these patients show genetic polymorphisms that are associated with or contribute to the disease. 7883123 1995
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation disease BEFREE To investigate the prevalence of potential mutations in the gene encoding HKII, we used the polymerase chain reaction (PCR) to amplify each of the 18 exons of the HKII gene from genomic DNA derived from 59 subjects: 25 insulin-resistant probands with clinical features of the type A syndrome and 34 NIDDM subjects enrolled in the United Kingdom Prospective Study of Therapies of NIDDM (UKPDS) who represented the highest percentile of fasting hyperinsulinemia in the UKPDS population of 5,098 subjects. 7883122 1995
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.050 GeneticVariation disease BEFREE To investigate the prevalence of potential mutations in the gene encoding HKII, we used the polymerase chain reaction (PCR) to amplify each of the 18 exons of the HKII gene from genomic DNA derived from 59 subjects: 25 insulin-resistant probands with clinical features of the type A syndrome and 34 NIDDM subjects enrolled in the United Kingdom Prospective Study of Therapies of NIDDM (UKPDS) who represented the highest percentile of fasting hyperinsulinemia in the UKPDS population of 5,098 subjects. 7883122 1995
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
0.010 AlteredExpression phenotype BEFREE Here we report decreased HK2 enzyme activity in skeletal muscle biopsies from patients with impaired glucose tolerance compared with healthy control subjects (2.7 +/- 0.9 vs 4.9 +/- 1.1 nmol.min-1.mg protein-1). 8786021 1995
Diabetes Mellitus, Non-Insulin-Dependent
0.100 Biomarker disease BEFREE These results suggest that the HKII, GLP1R, FABP-2, and apoC-II genes are not the major inherited factors for the development of Type 2 diabetes or IGT in Japanese subjects, although minor contribution cannot be ruled out. 8911786 1996
Diabetes Mellitus, Non-Insulin-Dependent
0.100 Biomarker disease BEFREE As HKII is a candidate gene that could contribute to the manifestation of insulin resistance and NIDDM, we genotyped 1152 Pima Indians, a Native American tribe that has the highest reported prevalence of NIDDM in the world. 8834247 1996
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation disease BEFREE (1) mutations in the coding regions of the HKII gene are unlikely to be major determinants in the development of insulin resistance and familial NIDDM; although (2) the influence of the codon 142 mutation in combination with other abnormalities of the insulin-signalling pathway on insulin action remain to be addressed. 8721778 1996
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.030 AlteredExpression disease BEFREE However, glucose phosphorylation can represent a rate-limiting step for skeletal muscle glucose utilization since muscle glucose-6-phosphate levels are increased during in vivo hyperinsulinemia and hyperglycemia; furthermore, basal and insulin-mediated muscle glucose uptake can be increased by a selective increase in HKII expression. 8662926 1996
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation disease BEFREE The human hexokinase II gene promoter: functional characterization and detection of variants among patients with NIDDM. 9447955 1997
CUI: C0028754
Disease: Obesity
Obesity
0.520 AlteredExpression disease BEFREE The purpose of this study was to determine whether defects in insulin-stimulated HKII expression and activity could contribute to the insulin resistance of obesity and NIDDM. 9519744 1998
Diabetes Mellitus, Non-Insulin-Dependent
0.100 AlteredExpression disease BEFREE In response to 40 mU insulin, HKII mRNA in lean control subjects was increased 1.48 +/- 0.18-fold (P < 0.05) but failed to increase significantly in the obese (1.12 +/- 0.24) or NIDDM (1.14 +/- 0.18) groups. 9519744 1998
Diabetes Mellitus, Non-Insulin-Dependent
0.100 Biomarker disease BEFREE Hexokinase II (HKII) catalyses a key step in glucose metabolism and can be regarded as a candidate gene for insulin resistance and type 2 (non-insulin-dependent) diabetes mellitus. 9794109 1998
CUI: C0023896
Disease: Alcoholic Liver Diseases
Alcoholic Liver Diseases
0.010 AlteredExpression group BEFREE The activity of hexokinase II was increased approximately 7-fold in alcoholic liver disease. 9468341 1998
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE This represents a novel use of the hexokinase type II as a selective promoter in cancer gene therapy. 10022541 1999
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.100 Biomarker group BEFREE This represents a novel use of the hexokinase type II as a selective promoter in cancer gene therapy. 10022541 1999
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.100 PosttranslationalModification disease BEFREE Our data suggest that the expression of the hK2 gene in breast cancer cell lines is mainly under the control of androgens and progestins, similarly to PSA. 10832596 2000
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.100 PosttranslationalModification disease BEFREE Our data suggest that the expression of the hK2 gene in breast cancer cell lines is mainly under the control of androgens and progestins, similarly to PSA. 10832596 2000
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.050 AlteredExpression disease BEFREE The time course of the ability of hyperinsulinemia to increase HKII mRNA indicates that insulin is likely a physiological regulator of HKII expression in human skeletal muscle in vivo. 10877213 2000
CUI: C0028754
Disease: Obesity
Obesity
0.520 AlteredExpression disease BEFREE Glucose phosphorylation and HKII expression are both reduced in obese and type 2 diabetic subjects. 11319725 2001