PGLYRP2
peptidoglycan recognition protein 2
Summary
This gene encodes a peptidoglycan recognition protein, which belongs to the N-acetylmuramoyl-L-alanine amidase 2 family. This protein hydrolyzes the link between N-acetylmuramoyl residues and L-amino acid residues in bacterial cell wall glycopeptides, and thus may play a scavenger role by digesting biologically active peptidoglycan into biologically inactive fragments. [provided by RefSeq, Sep 2011]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2513104490 | 19:15,579,527 | T/C | — | uncertain significance |
| rs775595527 | 19:15,579,537 | A/C | — | likely benign |
| rs36020076 | 19:15,580,290 | G/T | — | — |
| rs1228145868 | 19:15,580,511 | G/T | — | uncertain significance |
| rs754845797 | 19:15,580,592 | T/C | — | uncertain significance |
| rs200967069 | 19:15,580,637 | C/T | — | uncertain significance |
| rs376090335 | 19:15,580,684 | C/T | — | uncertain significance |
| rs112620863 | 19:15,581,119 | C/G | — | — |
| rs60292400 | 19:15,582,380 | C/T | intron variant | — |
| rs12610560 | 19:15,582,485 | G/C | intron variant | — |
| rs1970753335 | 19:15,582,749 | A/C | — | uncertain significance |
| rs2513108539 | 19:15,582,845 | A/G | — | uncertain significance |
| rs4638719 | 19:15,583,562 | A/T | — | — |
| rs8105422 | 19:15,585,889 | A/G | intron variant | — |
| rs2513111560 | 19:15,586,426 | T/C | — | uncertain significance |
| rs1184724443 | 19:15,586,456 | A/C | — | uncertain significance |
| rs535549580 | 19:15,586,525 | C/T | — | uncertain significance |
| rs138928836 | 19:15,586,604 | G/A | — | uncertain significance |
| rs892145 | 19:15,586,672 | A/T | missense variant | — |
| rs28404490 | 19:15,586,711 | G/T | missense variant | — |
| rs144572782 | 19:15,586,780 | C/A | — | benign |
| rs200781547 | 19:15,586,783 | C/G | — | uncertain significance |
| rs765503342 | 19:15,586,807 | C/T | — | uncertain significance |
| rs770945818 | 19:15,586,886 | C/T | — | uncertain significance |
| rs1384966704 | 19:15,586,988 | C/T | — | uncertain significance |
| rs2513112478 | 19:15,587,042 | C/A | — | uncertain significance |
| rs145036720 | 19:15,587,051 | T/C | — | uncertain significance |
| rs747502920 | 19:15,587,077 | C/T | — | likely benign |
| rs374903560 | 19:15,587,156 | C/G | — | uncertain significance |
| rs749892721 | 19:15,587,177 | C/T | — | uncertain significance |
| rs733731 | 19:15,587,185 | C/G | missense variant | — |
| rs3813135 | 19:15,587,345 | T/G | missense variant | — |
| rs554076198 | 19:15,588,244 | C/T | — | — |
| rs111242544 | 19:15,588,280 | G/A | intron variant | — |
| rs781259350 | 19:15,590,152 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.