PDCD1LG2
programmed cell death 1 ligand 2
Summary
Involved in negative regulation of activated T cell proliferation; negative regulation of interleukin-10 production; and negative regulation of type II interferon production. Predicted to be located in plasma membrane. Predicted to be active in external side of plasma membrane. Biomarker of pulmonary tuberculosis. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs141265736 | 9:5,508,987 | G/A | — | — |
| rs185199691 | 9:5,509,196 | G/T | upstream gene variant | — |
| rs577214809 | 9:5,522,173 | G/C | — | — |
| rs1037381642 | 9:5,522,598 | G/C | — | uncertain significance |
| rs779657826 | 9:5,522,599 | C/T | — | uncertain significance |
| rs189772690 | 9:5,528,045 | G/T | intron variant | — |
| rs77316406 | 9:5,528,923 | T/A | intron variant | — |
| rs555131399 | 9:5,532,785 | T/C | — | — |
| rs373050561 | 9:5,534,852 | A/C | — | likely benign |
| rs948916084 | 9:5,534,853 | T/C | — | uncertain significance |
| rs2129794179 | 9:5,534,900 | G/A | — | uncertain significance |
| rs376982371 | 9:5,534,960 | C/G | — | uncertain significance |
| rs57753863 | 9:5,543,534 | G/C | intron variant | — |
| rs145634667 | 9:5,545,911 | G/A | intron variant | — |
| rs1208687109 | 9:5,549,351 | A/G | — | uncertain significance |
| rs2129874104 | 9:5,549,363 | C/G | — | uncertain significance |
| rs535770193 | 9:5,549,413 | G/A | — | uncertain significance |
| rs768123989 | 9:5,549,415 | T/A | — | uncertain significance |
| rs774062534 | 9:5,549,421 | C/G | — | uncertain significance |
| rs774533109 | 9:5,549,527 | C/T | — | uncertain significance |
| rs138254251 | 9:5,549,568 | G/A | — | likely benign |
| rs770915970 | 9:5,557,629 | C/T | — | uncertain significance |
| rs7854413 | 9:5,557,708 | T/C | missense variant | — |
| rs139007200 | 9:5,557,726 | T/A | — | uncertain significance |
| rs1816599755 | 9:5,563,171 | A/C | — | uncertain significance |
| rs142289553 | 9:5,569,954 | A/G | — | uncertain significance |
| rs73641643 | 9:5,570,944 | C/T | 3 prime UTR variant | — |
| rs141281211 | 9:5,571,417 | C/G | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.