| ID | Sequence | Length | GC content |
|---|---|---|---|
| AUCAAAGCAGCGGCCGGCUGUUGGGGUCCACCACGCCUUCCACCUGCCC… | 467 nt | 0.5353 | |
| AUCAAAGCAGCGGCCGGCUGUUGGGGUCCACCACGCCUUCCACCUGCCC… | 425 nt | 0.5294 |
Predicted to enable zinc ion binding activity. Involved in cellular response to cadmium ion and cellular response to zinc ion. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
A study in human HT-29 colorectal adenocarcinoma cells demonstrated that the MT1F was highly induced (138.6-fold) by arsenic trioxide exposure, with dose-dependent upregulation confirmed by qRT-PCR [Kazuta et al. DOI:10.1016/J.Legalmed.2026.102774]. In a separate investigation of human post-mortem tissues from septic shock patients, the MT1F was found to be upregulated in the prefrontal cortex and heart [Pinheiro da Silva et al. DOI:10.1111/jcmm.17938]. A study in mice demonstrated that internal exposure to α-particles, specifically targeting Kupffer and endothelial cells in the liver, induced a characteristic inflammatory state and altered gene expression profiles [Roudkenar et al. DOI:10.1269/jrr.07078].