AP1B1
adaptor related protein complex 1 subunit beta 1
Summary
Adaptor protein complex 1 is found at the cytoplasmic face of coated vesicles located at the Golgi complex, where it mediates both the recruitment of clathrin to the membrane and the recognition of sorting signals within the cytosolic tails of transmembrane receptors. This complex is a heterotetramer composed of two large, one medium, and one small adaptin subunit. The protein encoded by this gene serves as one of the large subunits of this complex and is a member of the adaptin protein family. This gene is a candidate meningioma gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Known Variants82 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs74339735 | 22:29,724,664 | G/A | — | benign |
| rs6006095 | 22:29,724,792 | T/C | — | benign |
| rs758116414 | 22:29,724,881 | A/T | — | uncertain significance |
| rs142354304 | 22:29,726,395 | C/T | — | likely benign |
| rs905377582 | 22:29,726,411 | C/A | — | uncertain significance |
| rs764213357 | 22:29,726,420 | C/T | — | uncertain significance |
| rs2517758542 | 22:29,726,456 | G/A | — | pathogenic |
| rs754456794 | 22:29,726,465 | C/T | — | uncertain significance |
| rs1003185341 | 22:29,726,473 | T/C | — | uncertain significance |
| rs1210359734 | 22:29,726,498 | T/C | — | uncertain significance |
| rs2061540908 | 22:29,726,509 | C/A | — | uncertain significance |
| rs763612751 | 22:29,726,623 | G/C | — | uncertain significance |
| rs2517761853 | 22:29,727,433 | C/T | — | likely benign |
| rs780548317 | 22:29,727,841 | C/A | — | pathogenic |
| rs174765 | 22:29,727,866 | T/C | — | benign |
| rs776653588 | 22:29,727,880 | G/C | — | uncertain significance |
| rs2517764457 | 22:29,727,904 | A/G | — | uncertain significance |
| rs2061565545 | 22:29,727,908 | G/C | — | uncertain significance |
| rs376007379 | 22:29,730,246 | G/A | — | likely benign |
| rs537706062 | 22:29,730,300 | C/A | — | uncertain significance |
| rs2147939173 | 22:29,730,304 | G/T | — | uncertain significance |
| rs1395587910 | 22:29,730,347 | G/A | — | uncertain significance |
| rs775761249 | 22:29,730,407 | G/A | — | likely benign |
| rs98069 | 22:29,730,625 | A/G | — | benign |
| rs6006098 | 22:29,734,797 | G/A | — | benign |
| rs59074009 | 22:29,734,952 | C/T | — | benign |
| rs2517783079 | 22:29,735,025 | G/A | — | uncertain significance |
| rs145640648 | 22:29,735,056 | C/T | — | uncertain significance |
| rs935308292 | 22:29,735,077 | C/G | — | uncertain significance |
| rs3747146 | 22:29,735,310 | T/C | — | benign |
| rs34583478 | 22:29,735,647 | C/T | — | benign |
| rs2228323 | 22:29,736,660 | A/G | — | benign |
| rs572161344 | 22:29,736,725 | G/T | — | uncertain significance |
| rs1334834057 | 22:29,736,791 | G/A | — | pathogenic |
| rs750467942 | 22:29,736,815 | G/C | — | uncertain significance |
| rs139231493 | 22:29,736,816 | G/C | — | likely benign |
| rs754226007 | 22:29,736,836 | C/T | — | likely benign |
| rs776595684 | 22:29,737,499 | C/T | — | uncertain significance |
| rs149960917 | 22:29,737,521 | C/T | — | likely benign |
| rs760162142 | 22:29,737,536 | C/G | — | uncertain significance |
| rs200628910 | 22:29,737,551 | T/C | — | likely benign |
| rs1245595086 | 22:29,737,722 | G/C | — | uncertain significance |
| rs771243553 | 22:29,737,749 | C/A | — | uncertain significance |
| rs75220707 | 22:29,737,788 | G/C | — | benign |
| rs2301587 | 22:29,737,823 | T/C | — | benign |
| rs7285200 | 22:29,738,546 | C/T | — | benign |
| rs112869404 | 22:29,745,032 | T/G | — | benign |
| rs114122511 | 22:29,745,077 | C/T | — | benign |
| rs780846849 | 22:29,745,271 | C/T | — | uncertain significance |
| rs543593960 | 22:29,745,308 | C/T | — | likely benign |
| rs1183324698 | 22:29,745,364 | C/A | — | uncertain significance |
| rs2147978539 | 22:29,746,032 | G/T | — | pathogenic |
| rs140314768 | 22:29,746,062 | G/A | — | likely benign |
| rs737883 | 22:29,746,253 | C/T | — | benign |
| rs143474762 | 22:29,747,180 | G/A | — | uncertain significance |
| rs756010735 | 22:29,747,228 | T/C | — | uncertain significance |
| rs79760348 | 22:29,747,412 | A/C | — | benign |
| rs199663865 | 22:29,747,699 | C/T | — | uncertain significance |
| rs148745544 | 22:29,747,766 | G/A | — | likely benign |
| rs747391498 | 22:29,750,657 | T/C | — | uncertain significance |
| rs1010374023 | 22:29,750,666 | C/T | — | uncertain significance |
| rs200526044 | 22:29,750,817 | C/T | — | uncertain significance |
| rs6006103 | 22:29,751,030 | G/C | — | benign |
| rs140871358 | 22:29,752,427 | C/T | — | likely benign |
| rs754647389 | 22:29,752,431 | C/T | — | uncertain significance |
| rs201826297 | 22:29,752,444 | A/G | — | likely benign |
| rs2147995205 | 22:29,752,463 | A/G | — | pathogenic |
| rs1569159579 | 22:29,752,494 | C/T | — | uncertain significance |
| rs1013785497 | 22:29,752,553 | C/T | — | uncertain significance |
| rs570779704 | 22:29,752,566 | C/G | — | uncertain significance |
| rs76798358 | 22:29,752,785 | A/G | — | benign |
| rs1602749299 | 22:29,754,810 | A/G | — | pathogenic |
| rs1160266009 | 22:29,754,918 | G/A | — | pathogenic |
| rs143484030 | 22:29,755,831 | G/A | — | likely benign |
| rs2072051 | 22:29,755,888 | T/C | — | benign |
| rs4611747 | 22:29,757,090 | C/T | regulatory region variant | — |
| rs570731 | 22:29,758,817 | A/G | — | benign |
| rs8138200 | 22:29,758,963 | G/T | — | benign |
| rs1602761438 | 22:29,759,096 | C/T | — | pathogenic |
| rs6006105 | 22:29,759,188 | C/G | — | benign |
| rs2148022135 | 22:29,763,231 | A/G | — | likely pathogenic |
| rs4034938 | 22:29,763,451 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.