Browse our INSIG2 Proteins (INSIG2)

Human Insulin Induced Gene 2 (INSIG2) interaction partners

1. IINSIG2 gene single nucleotide polymorphisms and global DNA methylation (show HELLS Proteins) are linked with weight loss in obese patients.

2. INSIG2 plays a role in weight gain and obesity during clozapine treatment

3. These results indicate that HIF-mediated induction of Insig-2 and degradation of HMGCR (show HMGCR Proteins) are physiologically relevant events that guard against wasteful oxygen consumption and inappropriate cell growth during hypoxia.

4. There may be a connection between INSIG2 expression and metastatic dissemination of colorectal cancer without any effect on tumorigenesis.

5. Insulin (show INS Proteins) resistance in obese boys leads to up-regulation of INSIG2 gene expression as well as to down-regulation of PFKFB1 (show PFKFB1 Proteins), PFKFB3 (show PFKFB3 Proteins), and HK2 (show HK2 Proteins) genes in the blood cells as compared to obese patients with normal insulin (show INS Proteins) sensitivity.

6. Results confirmed that genetic variation in INSIG2 is associated with both overweight and LDL in non-Hispanic white children.

7. This study suggests that the G allele in the INSIG2 single nucleotide polymorphism rs7566605 is more relevant for changes in intramuscular adipose tissue following training than for the amount of subcutaneous fat.

8. INSIG2 is involved in adipogenesis and MC4R (show MC4R Proteins) effects hormonal appetite control in response to the amount of adipose tissue.

9. The results provided evidence for identifying genetic factors of nonalcoholic fatty liver disease (NAFLD) and may be useful for risk assessment and personalized medicine of NAFLD.

10. The INSIG2 rs7566605 SNP may not play a role in the development of obesity-related metabolic traits in Malaysian Malays.

Pig (Porcine) Insulin Induced Gene 2 (INSIG2) interaction partners

1. FASN (show FASN Proteins) gene is a promising marker for subcutaneous fat tissue accumulation, while INSIG2 is a promising marker for FA composition

Mouse (Murine) Insulin Induced Gene 2 (INSIG2) interaction partners

1. Intracellular biosynthesis of lipids and cholesterol by Scap and Insig in mesenchymal cells regulates long bone growth and chondrocyte homeostasis.

2. INSIG2 is a negative regulator of SREBP, and acute glucocorticoid treatment decreased active SREBP during refeeding or in livers of Ob/Ob mice, both systems of elevated SREBP-1c (show SREBF1 Proteins)-driven lipogenesis.

3. These results indicate that HIF-mediated induction of Insig-2 and degradation of HMGCR (show HMGCR Proteins) are physiologically relevant events that guard against wasteful oxygen consumption and inappropriate cell growth during hypoxia.

4. Data show that REV-ERBalpha (show NR1D1 Proteins) participates in the circadian modulation of SREBP activity, and the expression of SREBP target genes involved in cholesterol and lipid metabolism via the cyclic transcription of Insig2.

5. Liver-specific mRNA for Insig-2 down-regulated by insulin (show INS Proteins): implications for fatty acid synthesis.

6. a vitamin D response element in the murine Insig-2 promoter may have a role in the differentiation of 3T3-L1 preadipocytes

7. Insig2 identified as a strong candidate susceptibility gene for total plasma cholesterol levelsin inbred mice strains

8. Treatment of pregnant mice with the HMG-CoA reductase (show HMGCR Proteins) inhibitor lovastatin reduced sterol synthesis in Insig2-knockout embryos and reduced the pre-cholesterol intermediates ameliorating the clefting.

9. A critical gene involved in cholesterol homeostasis, Insig-2, was induced when mice or cultured cells were treated with FXRalpha (show NR1H4 Proteins) agonists or infected with constitutively active FXRalpha (show NR1H4 Proteins).

10. Peroxisome deficiency causes a complex phenotype because of hepatic SREBP-1c (show SREBF1 Proteins),-2/Insig-2a,b dysregulation associated with endoplasmic reticulum stress