REEP3
receptor accessory protein 3
Summary
Predicted to enable microtubule binding activity. Involved in mitotic nuclear membrane reassembly. Predicted to be located in endoplasmic reticulum; membrane; and microtubule. Predicted to be active in cytoplasmic microtubule; endoplasmic reticulum membrane; and endoplasmic reticulum tubular network. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7075901 | 10:65,280,994 | C/A | regulatory region variant | — |
| rs7085018 | 10:65,286,667 | T/C | intron variant | — |
| rs188925022 | 10:65,290,970 | C/T | intron variant | — |
| rs7920058 | 10:65,293,924 | T/G | intron variant | — |
| rs80264007 | 10:65,294,778 | G/T | intron variant | — |
| rs573770038 | 10:65,296,467 | G/A | — | — |
| rs12257409 | 10:65,302,699 | C/T | intron variant | — |
| rs12263348 | 10:65,305,252 | C/T | intron variant | — |
| rs7100190 | 10:65,307,177 | T/C | intron variant | — |
| rs1991571 | 10:65,310,154 | C/A | intron variant | — |
| rs9919429 | 10:65,313,819 | A/C | — | — |
| rs2163188 | 10:65,314,711 | G/A | — | — |
| rs2393984 | 10:65,314,971 | A/T | — | — |
| rs12411988 | 10:65,315,397 | G/C | intron variant | — |
| rs10740134 | 10:65,315,433 | T/C | intron variant | — |
| rs7919685 | 10:65,315,800 | G/T | intron variant | — |
| rs74502455 | 10:65,316,437 | C/A | — | — |
| rs12247907 | 10:65,317,045 | G/T | — | — |
| rs10761785 | 10:65,318,766 | G/C | — | — |
| rs7898861 | 10:65,319,678 | T/C | intron variant | — |
| rs2393986 | 10:65,320,006 | A/G | — | — |
| rs12245149 | 10:65,321,147 | C/A | intron variant | — |
| rs12245367 | 10:65,321,464 | C/G | — | — |
| rs7899657 | 10:65,323,265 | G/A | intron variant | — |
| rs10822182 | 10:65,325,478 | G/T | — | — |
| rs766937672 | 10:65,326,159 | G/A | — | uncertain significance |
| rs2492164973 | 10:65,326,163 | A/C | — | uncertain significance |
| rs6479908 | 10:65,333,648 | C/G | intron variant | — |
| rs7077256 | 10:65,336,185 | A/G | intron variant | — |
| rs10822184 | 10:65,337,153 | T/G | — | — |
| rs7910951 | 10:65,338,304 | A/G | intron variant | — |
| rs7900131 | 10:65,351,534 | A/T | intron variant | — |
| rs10761787 | 10:65,353,755 | A/T | intron variant | — |
| rs200806624 | 10:65,354,554 | A/T | — | uncertain significance |
| rs149136568 | 10:65,356,396 | A/G | intron variant | — |
| rs760168466 | 10:65,357,884 | C/G | — | uncertain significance |
| rs2492231090 | 10:65,359,038 | G/A | — | uncertain significance |
| rs372963754 | 10:65,369,968 | C/T | — | uncertain significance |
| rs10995569 | 10:65,370,041 | A/G | — | benign |
| rs755466573 | 10:65,370,064 | A/G | — | uncertain significance |
| rs10465964 | 10:65,378,806 | G/C | intron variant | — |
| rs750072566 | 10:65,379,420 | G/A | — | uncertain significance |
| rs373975658 | 10:65,379,501 | A/G | — | uncertain significance |
| rs1203134212 | 10:65,379,515 | A/G | — | likely benign |
| rs371406997 | 10:65,379,517 | C/T | — | uncertain significance |
| rs368723146 | 10:65,379,544 | C/G | — | uncertain significance |
| rs1368150192 | 10:65,380,577 | G/A | — | uncertain significance |
| rs767187683 | 10:65,380,610 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.