NAALADL2
N-acetylated alpha-linked acidic dipeptidase like 2
Summary
Predicted to act upstream of or within response to bacterium. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10936797 | 3:174,194,243 | T/G | intron variant | — |
| rs6764678 | 3:174,249,105 | T/C | intron variant | — |
| rs1423662667 | 3:174,480,093 | G/T | — | — |
| rs3914502 | 3:174,564,602 | T/C | — | — |
| rs2222447 | 3:174,580,826 | T/G | regulatory region variant | — |
| rs528826089 | 3:174,730,887 | A/T | — | — |
| rs11915224 | 3:174,801,986 | G/A | — | — |
| rs9813064 | 3:174,805,562 | A/G | intron variant | — |
| rs199754631 | 3:174,814,613 | A/G | — | uncertain significance |
| rs2475073627 | 3:174,814,631 | A/T | — | uncertain significance |
| rs768181461 | 3:174,814,765 | T/G | — | uncertain significance |
| rs759833088 | 3:174,814,793 | C/A | — | uncertain significance |
| rs575342355 | 3:174,814,824 | G/T | — | uncertain significance |
| rs199919300 | 3:174,814,891 | C/T | — | uncertain significance |
| rs1005131113 | 3:174,814,898 | A/G | — | uncertain significance |
| rs150099163 | 3:174,814,909 | G/A | — | likely benign |
| rs767320484 | 3:174,814,925 | G/A | — | uncertain significance |
| rs371006136 | 3:174,814,961 | T/C | — | uncertain significance |
| rs764863466 | 3:174,815,029 | T/C | — | uncertain significance |
| rs781228443 | 3:174,815,057 | C/G | — | uncertain significance |
| rs748389115 | 3:174,815,062 | G/C | — | uncertain significance |
| rs367765642 | 3:174,815,073 | G/C | — | uncertain significance |
| rs570279387 | 3:174,853,495 | C/T | — | — |
| rs17531088 | 3:174,893,775 | C/T | intron variant | — |
| rs564279849 | 3:174,919,128 | T/C | — | — |
| rs182698376 | 3:174,951,734 | C/G | — | uncertain significance |
| rs2529929685 | 3:174,951,742 | A/C | — | uncertain significance |
| rs369168988 | 3:174,951,774 | T/C | — | uncertain significance |
| rs1383557968 | 3:174,951,780 | C/T | — | uncertain significance |
| rs1242391644 | 3:174,951,860 | A/G | — | uncertain significance |
| rs2529933561 | 3:174,951,868 | G/A | — | likely benign |
| rs757546820 | 3:174,951,883 | T/A | — | uncertain significance |
| rs758498922 | 3:174,952,002 | G/T | — | likely benign |
| rs1463525 | 3:174,961,387 | T/C | intron variant | — |
| rs201574419 | 3:174,974,212 | G/A | — | uncertain significance |
| rs1749959247 | 3:174,974,246 | G/C | — | uncertain significance |
| rs746090493 | 3:175,042,007 | A/G | — | uncertain significance |
| rs2110436064 | 3:175,042,036 | G/T | — | uncertain significance |
| rs376170164 | 3:175,042,055 | C/T | — | uncertain significance |
| rs1383572035 | 3:175,042,099 | G/C | — | uncertain significance |
| rs2042126 | 3:175,055,759 | T/A | — | — |
| rs10936845 | 3:175,064,809 | G/A | regulatory region variant | — |
| rs6771725 | 3:175,075,109 | G/T | regulatory region variant | — |
| rs62287976 | 3:175,103,614 | G/T | intron variant | — |
| rs569628007 | 3:175,118,370 | A/G | — | — |
| rs1344783072 | 3:175,165,137 | G/A | — | uncertain significance |
| rs144915385 | 3:175,181,200 | G/A | — | likely benign |
| rs372099377 | 3:175,184,769 | C/T | — | uncertain significance |
| rs1413154116 | 3:175,184,898 | C/A | — | uncertain significance |
| rs80191780 | 3:175,189,480 | T/G | — | benign |
| rs770621881 | 3:175,189,488 | G/A | — | uncertain significance |
| rs74619861 | 3:175,223,896 | G/A | intron variant | — |
| rs78943174 | 3:175,252,736 | C/T | intron variant | — |
| rs2545882956 | 3:175,293,835 | A/T | — | uncertain significance |
| rs1387085880 | 3:175,293,854 | G/A | — | uncertain significance |
| rs367650158 | 3:175,293,856 | G/C | — | uncertain significance |
| rs199849033 | 3:175,293,892 | A/G | — | uncertain significance |
| rs201229751 | 3:175,293,957 | G/C | — | uncertain significance |
| rs1056943241 | 3:175,345,080 | G/A | — | uncertain significance |
| rs151001242 | 3:175,345,085 | A/G | — | uncertain significance |
| rs1238133486 | 3:175,455,155 | A/G | — | uncertain significance |
| rs375780484 | 3:175,473,049 | C/T | — | uncertain significance |
| rs2546628846 | 3:175,473,065 | C/T | — | uncertain significance |
| rs770673045 | 3:175,473,127 | C/T | — | uncertain significance |
| rs774125225 | 3:175,473,128 | G/T | — | uncertain significance |
| rs369571444 | 3:175,473,138 | G/A | — | uncertain significance |
| rs1431612235 | 3:175,520,836 | A/G | — | uncertain significance |
| rs746685090 | 3:175,520,838 | A/G | — | uncertain significance |
| rs2546806988 | 3:175,520,869 | C/T | — | uncertain significance |
| rs752665150 | 3:175,520,886 | C/A | — | likely benign |
| rs1408248673 | 3:175,520,918 | G/A | — | uncertain significance |
| rs1408575182 | 3:175,520,927 | C/T | — | uncertain significance |
| rs368404405 | 3:175,520,966 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.