PHLDB2
pleckstrin homology like domain family B member 2
Summary
Enables cadherin binding activity. Involved in several processes, including negative regulation of focal adhesion assembly; regulation of cytoskeleton organization; and regulation of embryonic development. Located in several cellular components, including basal cortex; cytoskeleton; and focal adhesion. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants84 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs28675079 | 3:111,500,002 | G/A | intron variant | — |
| rs9843288 | 3:111,504,556 | T/A | intron variant | — |
| rs9880495 | 3:111,525,552 | T/C | — | — |
| rs9829968 | 3:111,535,358 | T/A | intron variant | — |
| rs377738910 | 3:111,564,743 | G/A | — | uncertain significance |
| rs1282980 | 3:111,572,321 | T/C | intron variant | — |
| rs73228543 | 3:111,592,838 | G/A | regulatory region variant | — |
| rs565987391 | 3:111,602,979 | G/C | — | uncertain significance |
| rs1036976125 | 3:111,603,034 | G/A | — | uncertain significance |
| rs373363961 | 3:111,603,036 | C/G | — | uncertain significance |
| rs538814161 | 3:111,603,055 | C/T | — | uncertain significance |
| rs34251436 | 3:111,603,061 | G/T | — | benign |
| rs370080216 | 3:111,603,217 | G/A | — | uncertain significance |
| rs201726425 | 3:111,603,252 | C/T | — | uncertain significance |
| rs2066075530 | 3:111,603,300 | G/A | — | uncertain significance |
| rs758062645 | 3:111,603,318 | A/G | — | uncertain significance |
| rs746815740 | 3:111,603,325 | G/A | — | uncertain significance |
| rs757190870 | 3:111,603,330 | A/G | — | uncertain significance |
| rs143220265 | 3:111,603,355 | A/T | — | uncertain significance |
| rs764672070 | 3:111,603,398 | T/A | — | uncertain significance |
| rs974459206 | 3:111,603,459 | A/G | — | uncertain significance |
| rs75357207 | 3:111,603,496 | C/T | — | benign |
| rs2472639259 | 3:111,603,540 | A/C | — | uncertain significance |
| rs375715630 | 3:111,603,557 | G/A | — | uncertain significance |
| rs753762885 | 3:111,603,576 | G/T | — | uncertain significance |
| rs553169056 | 3:111,603,577 | C/T | — | uncertain significance |
| rs200941711 | 3:111,603,598 | G/C | — | uncertain significance |
| rs1199884254 | 3:111,603,607 | A/G | — | uncertain significance |
| rs201171421 | 3:111,603,790 | A/G | — | uncertain significance |
| rs777463629 | 3:111,603,823 | A/G | — | uncertain significance |
| rs2066090269 | 3:111,603,927 | C/T | — | uncertain significance |
| rs1576993745 | 3:111,603,960 | A/G | — | uncertain significance |
| rs1171928721 | 3:111,603,963 | T/A | — | uncertain significance |
| rs372210288 | 3:111,604,045 | A/G | — | uncertain significance |
| rs202130294 | 3:111,604,057 | C/T | — | uncertain significance |
| rs201726032 | 3:111,604,158 | C/G | — | uncertain significance |
| rs779212442 | 3:111,604,212 | C/T | — | uncertain significance |
| rs772379628 | 3:111,604,215 | C/T | — | uncertain significance |
| rs1632032 | 3:111,613,902 | G/A | — | — |
| rs749757991 | 3:111,632,175 | C/T | — | uncertain significance |
| rs776695261 | 3:111,632,227 | G/A | — | uncertain significance |
| rs1449684219 | 3:111,632,269 | A/G | — | uncertain significance |
| rs200460122 | 3:111,632,422 | G/A | — | uncertain significance |
| rs1287508953 | 3:111,632,481 | C/T | — | uncertain significance |
| rs756953272 | 3:111,632,485 | C/T | — | uncertain significance |
| rs35775235 | 3:111,632,498 | C/T | — | benign |
| rs2472811536 | 3:111,632,512 | C/T | — | uncertain significance |
| rs546327397 | 3:111,632,524 | C/G | — | uncertain significance |
| rs200159078 | 3:111,637,946 | A/G | — | uncertain significance |
| rs148898642 | 3:111,637,980 | G/T | — | uncertain significance |
| rs951660 | 3:111,638,132 | A/T | — | — |
| rs530700776 | 3:111,639,166 | A/T | — | uncertain significance |
| rs148809965 | 3:111,639,187 | T/C | — | uncertain significance |
| rs373785918 | 3:111,639,219 | C/T | — | uncertain significance |
| rs1234630010 | 3:111,658,397 | C/G | — | uncertain significance |
| rs371794973 | 3:111,658,436 | C/T | — | uncertain significance |
| rs200179934 | 3:111,664,140 | A/G | — | uncertain significance |
| rs35506232 | 3:111,664,191 | A/G | — | benign |
| rs201249374 | 3:111,667,840 | C/G | — | uncertain significance |
| rs141504836 | 3:111,667,867 | C/G | — | uncertain significance |
| rs148911785 | 3:111,667,900 | C/T | — | likely benign |
| rs34542209 | 3:111,667,901 | G/A | — | benign |
| rs2473056122 | 3:111,671,480 | C/T | — | uncertain significance |
| rs2473065154 | 3:111,672,807 | T/C | — | uncertain significance |
| rs79994265 | 3:111,672,822 | C/T | — | benign |
| rs530126533 | 3:111,672,823 | C/T | — | uncertain significance |
| rs1436280741 | 3:111,672,837 | G/T | — | uncertain significance |
| rs34081887 | 3:111,672,861 | C/T | — | benign |
| rs9850011 | 3:111,672,880 | C/T | — | benign |
| rs374054688 | 3:111,680,961 | A/G | — | uncertain significance |
| rs2473145415 | 3:111,685,464 | A/G | — | uncertain significance |
| rs144852755 | 3:111,685,533 | C/T | — | uncertain significance |
| rs148574792 | 3:111,685,534 | G/A | — | uncertain significance |
| rs1015141473 | 3:111,685,536 | C/A | — | uncertain significance |
| rs370795450 | 3:111,685,542 | G/A | — | uncertain significance |
| rs780250895 | 3:111,686,528 | C/T | — | uncertain significance |
| rs146545101 | 3:111,688,552 | C/T | — | uncertain significance |
| rs561310661 | 3:111,688,553 | G/A | — | uncertain significance |
| rs760955864 | 3:111,688,556 | A/C | — | uncertain significance |
| rs141317321 | 3:111,688,567 | C/T | — | uncertain significance |
| rs769750848 | 3:111,688,625 | C/T | — | uncertain significance |
| rs138093020 | 3:111,692,636 | A/G | — | uncertain significance |
| rs963732096 | 3:111,693,393 | A/C | — | uncertain significance |
| rs757140349 | 3:111,693,394 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.