NLN
neurolysin
Summary
This gene encodes a member of the metallopeptidase M3 protein family that cleaves neurotensin at the Pro10-Tyr11 bond, leading to the formation of neurotensin(1-10) and neurotensin(11-13). The encoded protein is likely involved in the termination of the neurotensinergic signal in the central nervous system and in the gastrointestinal tract.[provided by RefSeq, Jun 2010]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs112089614 | 5:65,042,818 | G/A | intron variant | — |
| rs555372750 | 5:65,054,423 | T/C | — | uncertain significance |
| rs746668151 | 5:65,054,458 | G/A | — | uncertain significance |
| rs1346741348 | 5:65,054,476 | G/A | — | uncertain significance |
| rs139431004 | 5:65,054,513 | C/T | — | uncertain significance |
| rs775046462 | 5:65,054,569 | G/A | — | uncertain significance |
| rs1332461457 | 5:65,054,585 | T/G | — | uncertain significance |
| rs2546259999 | 5:65,058,787 | T/A | — | uncertain significance |
| rs377453304 | 5:65,058,844 | C/A | — | uncertain significance |
| rs755712804 | 5:65,058,853 | C/G | — | uncertain significance |
| rs992349348 | 5:65,073,263 | G/A | — | uncertain significance |
| rs766932101 | 5:65,077,202 | A/C | — | uncertain significance |
| rs2546275075 | 5:65,077,211 | G/T | — | uncertain significance |
| rs2546275106 | 5:65,077,235 | C/T | — | uncertain significance |
| rs1759906401 | 5:65,081,654 | A/G | — | uncertain significance |
| rs1181777384 | 5:65,081,671 | A/T | — | uncertain significance |
| rs551434956 | 5:65,081,719 | C/T | — | uncertain significance |
| rs548598442 | 5:65,083,971 | T/G | — | uncertain significance |
| rs1197164417 | 5:65,084,158 | A/G | — | uncertain significance |
| rs1477498619 | 5:65,084,242 | C/A | — | uncertain significance |
| rs2546280987 | 5:65,084,302 | T/A | — | uncertain significance |
| rs147330128 | 5:65,088,349 | G/A | — | uncertain significance |
| rs376947821 | 5:65,088,372 | G/A | — | uncertain significance |
| rs201670063 | 5:65,088,405 | C/T | — | uncertain significance |
| rs373507441 | 5:65,088,423 | G/A | — | uncertain significance |
| rs772545743 | 5:65,088,459 | G/A | — | uncertain significance |
| rs375581122 | 5:65,088,464 | G/A | — | uncertain significance |
| rs755927998 | 5:65,093,989 | C/T | — | — |
| rs373497025 | 5:65,105,363 | G/C | — | uncertain significance |
| rs763794414 | 5:65,105,372 | G/T | — | uncertain significance |
| rs370323110 | 5:65,105,429 | G/A | — | likely benign |
| rs372513324 | 5:65,105,442 | G/A | — | uncertain significance |
| rs1389842923 | 5:65,105,487 | A/T | — | uncertain significance |
| rs181089957 | 5:65,105,879 | G/C | — | uncertain significance |
| rs748248450 | 5:65,105,884 | A/G | — | uncertain significance |
| rs145543140 | 5:65,105,886 | T/G | — | uncertain significance |
| rs2546298266 | 5:65,108,093 | C/T | — | uncertain significance |
| rs141444389 | 5:65,118,686 | G/C | — | uncertain significance |
| rs150853932 | 5:65,118,691 | G/A | — | uncertain significance |
| rs2546304985 | 5:65,118,723 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.