PSD3
pleckstrin and Sec7 domain containing 3
Summary
Predicted to enable guanyl-nucleotide exchange factor activity and phospholipid binding activity. Predicted to be involved in regulation of ARF protein signal transduction. Predicted to be located in membrane. Predicted to be active in glutamatergic synapse; postsynapse; and ruffle membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs763433107 | 8:18,393,290 | C/T | — | uncertain significance |
| rs551637019 | 8:18,393,317 | C/T | — | uncertain significance |
| rs370316194 | 8:18,393,347 | T/G | — | uncertain significance |
| rs774651657 | 8:18,393,350 | G/A | — | uncertain significance |
| rs199928869 | 8:18,393,371 | T/G | — | uncertain significance |
| rs1198432700 | 8:18,393,374 | G/A | — | uncertain significance |
| rs565516174 | 8:18,393,396 | C/T | — | uncertain significance |
| rs28651847 | 8:18,413,785 | G/A | — | benign |
| rs745313487 | 8:18,413,814 | C/T | — | uncertain significance |
| rs746665443 | 8:18,413,824 | C/A | — | uncertain significance |
| rs563340531 | 8:18,413,853 | G/T | — | uncertain significance |
| rs377209838 | 8:18,430,067 | G/C | — | uncertain significance |
| rs769536182 | 8:18,430,076 | G/A | — | uncertain significance |
| rs2536247107 | 8:18,430,094 | A/C | — | uncertain significance |
| rs1802210420 | 8:18,430,096 | C/T | — | uncertain significance |
| rs1197253434 | 8:18,430,175 | C/T | — | uncertain significance |
| rs544501576 | 8:18,432,671 | G/C | — | uncertain significance |
| rs2536267408 | 8:18,432,687 | C/T | — | uncertain significance |
| rs774815173 | 8:18,432,719 | G/C | — | uncertain significance |
| rs200826970 | 8:18,432,788 | T/G | — | uncertain significance |
| rs2634458 | 8:18,458,446 | G/C | intron variant | — |
| rs2536629375 | 8:18,490,146 | T/C | — | uncertain significance |
| rs887918550 | 8:18,490,185 | G/C | — | uncertain significance |
| rs1806986825 | 8:18,490,207 | C/T | — | uncertain significance |
| rs376989905 | 8:18,490,236 | C/T | — | uncertain significance |
| rs1476397788 | 8:18,490,278 | G/C | — | uncertain significance |
| rs771292368 | 8:18,622,970 | C/A | — | uncertain significance |
| rs2537419144 | 8:18,623,006 | G/C | — | uncertain significance |
| rs2537419196 | 8:18,623,011 | G/T | — | uncertain significance |
| rs762791537 | 8:18,623,026 | C/A | — | uncertain significance |
| rs11203995 | 8:18,629,373 | C/T | downstream gene variant | — |
| rs118027861 | 8:18,629,826 | C/T | downstream gene variant | — |
| rs335251 | 8:18,647,338 | G/A | — | — |
| rs750869677 | 8:18,656,832 | C/A | — | uncertain significance |
| rs376601587 | 8:18,656,863 | T/C | — | uncertain significance |
| rs2537797896 | 8:18,658,789 | C/T | — | uncertain significance |
| rs201058269 | 8:18,658,794 | G/A | — | uncertain significance |
| rs745505856 | 8:18,658,795 | T/C | — | uncertain significance |
| rs143901818 | 8:18,658,878 | G/T | — | benign |
| rs1811057067 | 8:18,662,329 | C/T | — | uncertain significance |
| rs2537850424 | 8:18,662,331 | G/T | — | uncertain significance |
| rs749952868 | 8:18,662,370 | G/A | — | uncertain significance |
| rs377004772 | 8:18,662,386 | G/A | — | uncertain significance |
| rs35222739 | 8:18,662,399 | C/T | — | benign |
| rs73595761 | 8:18,662,625 | A/G | downstream gene variant | — |
| rs2638663 | 8:18,673,731 | T/G | intron variant | — |
| rs7833787 | 8:18,707,871 | A/T | — | — |
| rs1181976229 | 8:18,725,187 | C/T | — | uncertain significance |
| rs62636654 | 8:18,725,224 | T/G | — | benign |
| rs199505605 | 8:18,725,253 | G/A | — | likely benign |
| rs201772657 | 8:18,725,430 | G/A | — | uncertain significance |
| rs28645392 | 8:18,725,557 | C/A | — | benign |
| rs2538430673 | 8:18,725,577 | A/T | — | uncertain significance |
| rs548160525 | 8:18,729,201 | T/C | — | likely benign |
| rs114838869 | 8:18,729,227 | G/A | — | benign |
| rs73202143 | 8:18,729,328 | C/A | — | benign |
| rs146066561 | 8:18,729,350 | G/A | — | likely benign |
| rs377034597 | 8:18,729,426 | G/A | — | likely benign |
| rs201527530 | 8:18,729,593 | G/A | — | uncertain significance |
| rs139294568 | 8:18,729,702 | G/C | — | benign |
| rs760617193 | 8:18,729,739 | C/A | — | uncertain significance |
| rs542024957 | 8:18,729,842 | G/A | — | uncertain significance |
| rs947670136 | 8:18,729,878 | C/A | — | uncertain significance |
| rs187490678 | 8:18,729,933 | G/A | — | benign |
| rs1586289298 | 8:18,729,937 | A/G | — | uncertain significance |
| rs59099976 | 8:18,729,955 | G/A | — | benign |
| rs201964200 | 8:18,730,036 | T/A | — | likely benign |
| rs183792270 | 8:18,730,062 | G/A | — | likely benign |
| rs758450614 | 8:18,730,178 | T/C | — | uncertain significance |
| rs4921617 | 8:18,782,047 | C/T | intron variant | — |
| rs116031741 | 8:18,871,987 | T/A | — | — |
| rs567010138 | 8:18,903,930 | C/A | — | — |
| rs2410601 | 8:18,922,577 | G/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.