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FTO |
LOCUS ID | 79068 | |||||||||||||||||||
GENE_SYMBOL | FTO | |||||||||||||||||||
GENE NAME | fat mass and obesity | |||||||||||||||||||
SYNONYMNS | ALKBH9 | |||||||||||||||||||
CHROMOSOME | 16 | |||||||||||||||||||
HOMOLOGENE ID | 8053 |
microRNAs | NA | NA |
GENE SUMMARY |
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This gene is a nuclear protein of the AlkB related non-haem iron and 2-oxoglutarate-dependent oxygenase superfamily but the exact physiological function of this gene is not known. Other non-heme iron enzymes function to reverse alkylated D and R damage by oxidative demethylation. Studies in mice and humans indicate a role in nervous and cardiovascular systems and a strong association with body mass index, obesity risk, and type 2 diabetes. [provided by RefSeq, Jul 2011] |
OBSERVATIONS |
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Complication | Evidence | PMID |
Nephropathy | 1. JAZF1, FTO, CDKAL1, and HHEX/IDE are associated with diabetic nephropathy | 23298195 |
Cardiovascular | 1. WFS1, CDKN2A/B, CDC123/CAMK1D, JAZF1, FTO, CDKAL1, and HHEX/IDE are associated with cardiovascular risk. | 23298195 |
Retinopathy | 1. After stratification of patients according to the presence/absence of vascular complications, we found significant associations of variants in the CAT, FTO, and UCP1 genes with diabetic retinopathy and nephropathy. | 29410390 |
Insulin resistance and Inflammation | 1. Results of our study showed a significant association of?FTO?genetic variant rs8050136 A>C with the major markers of insulin resistance, obesity and inflammation, opening new avenues for solving many unclear questions in the pathogenesis of T2D. | 30867643 |