NT5DC2
5'-nucleotidase domain containing 2
Summary
Predicted to enable 5'-nucleotidase activity. Predicted to be involved in negative regulation of dopamine biosynthetic process; negative regulation of oxidoreductase activity; and negative regulation of peptidyl-serine phosphorylation. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs768627428 | 3:52,558,533 | C/T | — | uncertain significance |
| rs752980175 | 3:52,558,577 | G/A | — | uncertain significance |
| rs773032053 | 3:52,558,610 | C/T | — | uncertain significance |
| rs777510011 | 3:52,558,846 | G/A | — | uncertain significance |
| rs144568381 | 3:52,558,854 | A/T | — | uncertain significance |
| rs749388964 | 3:52,558,870 | C/A | — | uncertain significance |
| rs754871503 | 3:52,559,028 | T/C | missense variant | — |
| rs143799471 | 3:52,559,042 | C/T | synonymous variant | — |
| rs746426628 | 3:52,559,064 | C/T | — | uncertain significance |
| rs1421721260 | 3:52,559,078 | G/C | — | uncertain significance |
| rs201549406 | 3:52,559,085 | G/A | — | uncertain significance |
| rs747318346 | 3:52,559,101 | C/A | — | uncertain significance |
| rs780544534 | 3:52,559,113 | T/A | — | uncertain significance |
| rs749124845 | 3:52,559,263 | C/T | — | uncertain significance |
| rs200773348 | 3:52,559,266 | G/A | — | uncertain significance |
| rs779159546 | 3:52,559,275 | G/A | — | uncertain significance |
| rs750636981 | 3:52,559,290 | G/A | — | uncertain significance |
| rs200789146 | 3:52,561,348 | G/A | — | uncertain significance |
| rs764872514 | 3:52,561,697 | G/A | — | uncertain significance |
| rs2471681479 | 3:52,561,715 | T/C | — | uncertain significance |
| rs11711421 | 3:52,561,779 | C/T | downstream gene variant | — |
| rs772754777 | 3:52,562,054 | C/T | — | uncertain significance |
| rs1472165911 | 3:52,562,245 | C/G | — | uncertain significance |
| rs749231831 | 3:52,562,292 | C/T | — | likely benign |
| rs1186099999 | 3:52,562,654 | T/C | — | uncertain significance |
| rs567488297 | 3:52,562,663 | T/C | — | uncertain significance |
| rs1353861888 | 3:52,562,665 | C/A | — | uncertain significance |
| rs964254955 | 3:52,562,677 | T/C | — | uncertain significance |
| rs139119664 | 3:52,562,886 | G/A | — | likely benign |
| rs761029564 | 3:52,562,899 | C/A | — | uncertain significance |
| rs774970480 | 3:52,562,935 | C/T | — | uncertain significance |
| rs147863928 | 3:52,563,191 | C/T | — | uncertain significance |
| rs141804495 | 3:52,563,210 | C/T | — | uncertain significance |
| rs140922822 | 3:52,563,300 | C/T | — | uncertain significance |
| rs376710546 | 3:52,563,339 | G/T | — | uncertain significance |
| rs4687625 | 3:52,563,718 | C/T | upstream gene variant | — |
| rs7636227 | 3:52,566,682 | G/A | regulatory region variant | — |
| rs12489732 | 3:52,566,820 | C/G | — | — |
| rs12489828 | 3:52,567,014 | G/A | — | — |
| rs28661185 | 3:52,567,188 | G/C | — | — |
| rs769430142 | 3:52,567,566 | G/C | — | uncertain significance |
| rs2471693067 | 3:52,567,575 | T/G | — | uncertain significance |
| rs865859187 | 3:52,567,633 | C/G | — | uncertain significance |
| rs1481708754 | 3:52,567,678 | A/G | — | uncertain significance |
| rs1559742429 | 3:52,567,722 | C/A | — | uncertain significance |
| rs2079391649 | 3:52,567,723 | G/C | — | uncertain significance |
| rs1427580942 | 3:52,567,741 | C/T | — | uncertain significance |
| rs192855409 | 3:52,567,794 | A/G | — | — |
| rs200182123 | 3:52,568,562 | G/T | — | uncertain significance |
| rs7639267 | 3:52,568,805 | G/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.