TENT2
terminal nucleotidyltransferase 2
Summary
Enables poly(A) RNA polymerase activity. Involved in histone mRNA catabolic process; mRNA 3'-end processing; and negative regulation of miRNA catabolic process. Predicted to be located in cytoplasm and nucleus. Predicted to be part of nuclear RNA-directed RNA polymerase complex. Predicted to be active in glutamatergic synapse; perforant pathway to dendrate granule cell synapse; and postsynapse. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs558841099 | 5:78,915,550 | C/T | — | uncertain significance |
| rs368560743 | 5:78,915,557 | T/G | — | uncertain significance |
| rs768263040 | 5:78,915,578 | T/A | — | uncertain significance |
| rs747513506 | 5:78,915,826 | A/C | — | uncertain significance |
| rs1289443969 | 5:78,919,085 | G/A | — | uncertain significance |
| rs146051766 | 5:78,919,134 | C/T | — | uncertain significance |
| rs754378350 | 5:78,919,211 | C/G | — | uncertain significance |
| rs761708010 | 5:78,919,257 | G/A | — | uncertain significance |
| rs767142070 | 5:78,919,260 | A/C | — | uncertain significance |
| rs151126262 | 5:78,936,975 | C/T | — | uncertain significance |
| rs2481249702 | 5:78,936,995 | A/T | — | uncertain significance |
| rs142138126 | 5:78,938,689 | G/A | — | uncertain significance |
| rs1236961149 | 5:78,938,694 | A/C | — | uncertain significance |
| rs6859704 | 5:78,943,648 | G/A | — | — |
| rs1791082349 | 5:78,944,442 | G/T | — | uncertain significance |
| rs200878934 | 5:78,944,960 | G/A | — | uncertain significance |
| rs1561524614 | 5:78,944,975 | G/C | — | uncertain significance |
| rs781564324 | 5:78,944,992 | A/T | — | uncertain significance |
| rs1367612396 | 5:78,952,781 | C/A | — | uncertain significance |
| rs150126386 | 5:78,952,822 | C/A | — | uncertain significance |
| rs2483797194 | 5:78,964,722 | T/G | — | uncertain significance |
| rs149306467 | 5:78,964,769 | G/A | — | uncertain significance |
| rs2483807740 | 5:78,964,776 | C/T | — | uncertain significance |
| rs769910476 | 5:78,964,797 | C/T | — | uncertain significance |
| rs909378373 | 5:78,964,841 | A/G | — | uncertain significance |
| rs182465936 | 5:78,966,392 | C/T | intron variant | — |
| rs1820169104 | 5:78,975,470 | G/A | — | uncertain significance |
| rs567873139 | 5:78,981,031 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.