| STH |
| LOCUS ID | 246744 | ||||||||||
| GENE_SYMBOL | STH | ||||||||||
| GENE NAME | saitohin | ||||||||||
| SYNONYMNS | MAPTIT | ||||||||||
| CHROMOSOME | 17 | ||||||||||
| HOMOLOGENE ID | 88448 |
| microRNAs | NA | NA |
| GENE SUMMARY |
|---|
| STH (Saitohin) is a Protein Coding gene. Diseases associated with STH include Frontotemporal Dementia and Chromosome 17Q21.31 Duplication Syndrome. |
| OBSERVATIONS |
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| Complication | Evidence | PMID |
| Nephropathy | 1. As compared with the subjects from a control group, STH in serum of diabetics without retinopathy, with retinopathy, with obesity and renal insufficiency resulting from nephropathy was increased with a statistical significance. | 7257332 |