PLLP
plasmolipin
Summary
Enables identical protein binding activity. Involved in myelin assembly and regulation of transcytosis. Located in myelin sheath and plasma membrane. Biomarker of schizophrenia. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs776743553 | 16:57,290,877 | C/T | — | uncertain significance |
| rs145234410 | 16:57,290,926 | C/T | — | uncertain significance |
| rs199759873 | 16:57,290,934 | G/A | — | uncertain significance |
| rs149171475 | 16:57,290,941 | A/G | — | uncertain significance |
| rs7194319 | 16:57,292,132 | G/T | downstream gene variant | — |
| rs754274845 | 16:57,292,375 | G/A | — | uncertain significance |
| rs751274703 | 16:57,292,384 | G/A | — | uncertain significance |
| rs1266996457 | 16:57,292,445 | C/T | — | likely benign |
| rs765916712 | 16:57,295,813 | A/G | — | uncertain significance |
| rs200960257 | 16:57,295,829 | T/C | — | uncertain significance |
| rs2545937948 | 16:57,295,834 | A/G | — | uncertain significance |
| rs142797341 | 16:57,295,901 | C/T | — | uncertain significance |
| rs985357032 | 16:57,295,904 | C/T | — | uncertain significance |
| rs35467222 | 16:57,295,952 | C/T | — | uncertain significance |
| rs60403102 | 16:57,297,312 | G/A | intron variant | — |
| rs78238999 | 16:57,299,858 | A/T | intron variant | — |
| rs4784786 | 16:57,301,605 | C/T | intron variant | — |
| rs11640439 | 16:57,303,194 | G/A | regulatory region variant | — |
| rs66514732 | 16:57,304,811 | T/C | intron variant | — |
| rs75075448 | 16:57,305,389 | C/G | intron variant | — |
| rs7197160 | 16:57,317,020 | C/A | — | — |
| rs117932065 | 16:57,318,078 | G/A | regulatory region variant | — |
| rs1901261400 | 16:57,318,432 | T/A | — | uncertain significance |
| rs1181276721 | 16:57,318,433 | T/C | — | uncertain significance |
| rs1481726531 | 16:57,318,437 | A/T | — | uncertain significance |
| rs7187527 | 16:57,319,143 | C/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.