NAALADL1
N-acetylated alpha-linked acidic dipeptidase like 1
Summary
Enables aminopeptidase activity; metal ion binding activity; and protein homodimerization activity. Involved in peptide catabolic process. Predicted to be located in apical plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs370097990 | 11:64,812,891 | G/A | — | uncertain significance |
| rs201373743 | 11:64,812,898 | C/T | — | uncertain significance |
| rs1402756135 | 11:64,813,301 | A/G | — | uncertain significance |
| rs139461439 | 11:64,813,304 | G/A | — | uncertain significance |
| rs144988552 | 11:64,813,307 | C/T | — | uncertain significance |
| rs74460041 | 11:64,813,340 | G/C | — | uncertain significance |
| rs201315473 | 11:64,813,373 | G/A | — | uncertain significance |
| rs756376050 | 11:64,813,529 | C/T | — | likely benign |
| rs1946723481 | 11:64,813,747 | C/G | — | uncertain significance |
| rs377372068 | 11:64,813,808 | G/A | — | uncertain significance |
| rs748031186 | 11:64,813,813 | A/G | — | uncertain significance |
| rs138345812 | 11:64,813,935 | C/A | — | uncertain significance |
| rs149583840 | 11:64,813,985 | G/A | — | uncertain significance |
| rs488686 | 11:64,814,425 | G/C | — | — |
| rs776565278 | 11:64,814,971 | C/G | — | uncertain significance |
| rs1946762452 | 11:64,814,972 | A/G | — | uncertain significance |
| rs1306062580 | 11:64,815,023 | C/A | — | uncertain significance |
| rs200312525 | 11:64,815,138 | C/T | — | uncertain significance |
| rs377514826 | 11:64,815,188 | T/C | — | likely benign |
| rs1421459366 | 11:64,815,203 | G/A | — | uncertain significance |
| rs139760307 | 11:64,815,499 | T/G | — | uncertain significance |
| rs778007946 | 11:64,815,648 | T/A | — | uncertain significance |
| rs757597014 | 11:64,815,650 | T/C | — | uncertain significance |
| rs149697032 | 11:64,815,794 | A/G | — | uncertain significance |
| rs148772939 | 11:64,820,738 | C/T | — | uncertain significance |
| rs2495517508 | 11:64,820,753 | G/T | — | uncertain significance |
| rs1047625136 | 11:64,820,990 | C/T | — | uncertain significance |
| rs146892159 | 11:64,821,023 | G/A | — | uncertain significance |
| rs1434944101 | 11:64,821,733 | G/C | — | uncertain significance |
| rs567066428 | 11:64,821,749 | C/T | — | uncertain significance |
| rs140919277 | 11:64,821,795 | A/G | — | uncertain significance |
| rs758730555 | 11:64,821,993 | T/C | — | uncertain significance |
| rs149308848 | 11:64,822,001 | G/T | — | uncertain significance |
| rs753580850 | 11:64,822,009 | G/A | — | uncertain significance |
| rs374086988 | 11:64,822,092 | G/A | — | uncertain significance |
| rs778274813 | 11:64,822,095 | G/T | — | uncertain significance |
| rs771177552 | 11:64,822,126 | C/T | — | likely benign |
| rs764028384 | 11:64,824,860 | C/T | — | uncertain significance |
| rs141128956 | 11:64,824,871 | C/T | — | uncertain significance |
| rs2495560272 | 11:64,824,874 | G/C | — | not provided |
| rs371191033 | 11:64,824,938 | C/T | — | likely benign |
| rs755770536 | 11:64,824,964 | C/T | — | uncertain significance |
| rs199800826 | 11:64,825,402 | C/G | — | uncertain significance |
| rs143826156 | 11:64,825,418 | C/T | — | uncertain significance |
| rs540364726 | 11:64,825,421 | T/C | — | uncertain significance |
| rs369881499 | 11:64,825,433 | G/A | — | uncertain significance |
| rs1289302270 | 11:64,825,579 | C/T | — | uncertain significance |
| rs139658894 | 11:64,825,601 | C/T | — | uncertain significance |
| rs749175914 | 11:64,825,616 | C/T | — | uncertain significance |
| rs536362910 | 11:64,825,627 | A/G | — | uncertain significance |
| rs549823233 | 11:64,825,652 | G/A | — | uncertain significance |
| rs142268835 | 11:64,825,822 | G/A | — | uncertain significance |
| rs764383436 | 11:64,825,872 | T/G | — | uncertain significance |
| rs199864491 | 11:64,825,877 | G/T | — | uncertain significance |
| rs753786831 | 11:64,825,881 | T/A | — | uncertain significance |
| rs778384658 | 11:64,825,890 | A/T | — | uncertain significance |
| rs752220561 | 11:64,825,909 | G/T | — | uncertain significance |
| rs765273619 | 11:64,825,983 | G/A | — | uncertain significance |
| rs144991069 | 11:64,827,708 | T/A | regulatory region variant | — |
| rs35661464 | 11:64,828,842 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.