PLIN5
perilipin 5
Summary
Predicted to enable identical protein binding activity and lipase binding activity. Predicted to be involved in several processes, including negative regulation of peroxisome proliferator activated receptor signaling pathway; positive regulation of triglyceride storage; and regulation of lipid metabolic process. Located in intracellular membrane-bounded organelle and lipid droplet. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758198765 | 19:4,523,545 | A/G | — | uncertain significance |
| rs1395252391 | 19:4,523,554 | C/G | — | uncertain significance |
| rs774771330 | 19:4,523,577 | G/A | — | uncertain significance |
| rs376263782 | 19:4,523,595 | G/A | — | uncertain significance |
| rs372681667 | 19:4,523,617 | C/T | — | uncertain significance |
| rs755684879 | 19:4,523,623 | C/A | — | uncertain significance |
| rs778692761 | 19:4,523,728 | C/A | — | uncertain significance |
| rs745654911 | 19:4,523,731 | C/T | — | uncertain significance |
| rs760540696 | 19:4,523,769 | G/T | — | uncertain significance |
| rs749529486 | 19:4,523,823 | G/A | — | uncertain significance |
| rs762489897 | 19:4,523,881 | C/T | — | uncertain significance |
| rs767931369 | 19:4,523,886 | C/T | — | uncertain significance |
| rs200877814 | 19:4,523,889 | C/T | missense variant | — |
| rs752949459 | 19:4,523,890 | G/A | — | uncertain significance |
| rs756530531 | 19:4,523,892 | C/T | — | uncertain significance |
| rs369891770 | 19:4,523,910 | G/A | — | uncertain significance |
| rs377657199 | 19:4,523,931 | C/T | — | uncertain significance |
| rs962429942 | 19:4,523,973 | C/T | — | uncertain significance |
| rs770718070 | 19:4,524,004 | C/T | — | uncertain significance |
| rs1025503817 | 19:4,524,015 | C/T | — | uncertain significance |
| rs963919694 | 19:4,524,035 | C/A | — | likely benign |
| rs1461103362 | 19:4,524,060 | G/A | — | uncertain significance |
| rs762421444 | 19:4,524,069 | C/A | — | uncertain significance |
| rs947593254 | 19:4,524,070 | G/A | — | uncertain significance |
| rs779669570 | 19:4,524,985 | C/A | — | uncertain significance |
| rs768365970 | 19:4,524,988 | C/T | — | uncertain significance |
| rs200382199 | 19:4,524,997 | G/A | — | likely benign |
| rs773617074 | 19:4,525,004 | G/A | — | likely benign |
| rs747789366 | 19:4,525,051 | G/A | — | uncertain significance |
| rs762891297 | 19:4,525,688 | C/A | — | uncertain significance |
| rs2512168061 | 19:4,525,769 | A/G | — | uncertain significance |
| rs138968629 | 19:4,527,379 | C/T | downstream gene variant | — |
| rs199498374 | 19:4,529,099 | G/A | — | uncertain significance |
| rs201001165 | 19:4,529,106 | G/C | — | uncertain significance |
| rs201819147 | 19:4,529,166 | C/T | — | likely benign |
| rs746844517 | 19:4,529,172 | G/A | — | uncertain significance |
| rs770558472 | 19:4,529,195 | C/G | — | uncertain significance |
| rs369901049 | 19:4,529,204 | C/T | — | uncertain significance |
| rs1976847221 | 19:4,529,235 | T/C | — | uncertain significance |
| rs2512170773 | 19:4,529,246 | T/A | — | uncertain significance |
| rs200136383 | 19:4,529,803 | G/A | — | uncertain significance |
| rs2512171626 | 19:4,529,810 | G/T | — | uncertain significance |
| rs372793168 | 19:4,529,857 | G/A | — | uncertain significance |
| rs138772557 | 19:4,531,658 | G/C | synonymous variant | — |
| rs750946143 | 19:4,531,672 | C/T | — | uncertain significance |
| rs574940044 | 19:4,531,677 | T/C | — | uncertain significance |
| rs780779953 | 19:4,531,705 | C/T | — | uncertain significance |
| rs897975377 | 19:4,531,731 | G/A | — | uncertain significance |
| rs781204109 | 19:4,531,774 | C/T | — | uncertain significance |
| rs771881511 | 19:4,531,783 | C/T | — | uncertain significance |
| rs747987953 | 19:4,531,791 | G/A | — | uncertain significance |
| rs375098526 | 19:4,531,821 | C/T | — | uncertain significance |
| rs768121130 | 19:4,531,831 | C/T | — | uncertain significance |
| rs372134676 | 19:4,534,083 | A/T | — | uncertain significance |
| rs182751279 | 19:4,535,182 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.