PODXL2
podocalyxin like 2
Summary
This gene is a member of the CD34 family of cell surface transmembrane proteins, which are characterized by an N-terminal extracellular mucin domain, globular and stalk domains, a single pass transmembrane region, and a charged cytoplasmic tail. The encoded protein is a ligand for vascular selectins. [provided by RefSeq, Oct 2012]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs74741864 | 3:127,347,514 | A/G | regulatory region variant | — |
| rs949242675 | 3:127,348,067 | G/A | — | uncertain significance |
| rs1352405376 | 3:127,348,069 | C/T | — | uncertain significance |
| rs553021480 | 3:127,348,087 | C/T | — | uncertain significance |
| rs1181590106 | 3:127,348,127 | T/G | — | uncertain significance |
| rs184821492 | 3:127,350,000 | G/T | intron variant | — |
| rs376308988 | 3:127,358,247 | C/G | — | uncertain significance |
| rs543898509 | 3:127,361,105 | C/G | — | — |
| rs769057384 | 3:127,379,268 | A/G | — | uncertain significance |
| rs2074757510 | 3:127,379,269 | C/G | — | uncertain significance |
| rs145087096 | 3:127,379,292 | A/G | — | uncertain significance |
| rs143584641 | 3:127,379,313 | A/G | missense variant | — |
| rs202139708 | 3:127,379,452 | G/A | — | uncertain significance |
| rs115568415 | 3:127,379,476 | A/G | — | uncertain significance |
| rs917473857 | 3:127,379,520 | G/A | — | uncertain significance |
| rs748594868 | 3:127,379,533 | G/A | — | likely benign |
| rs149151228 | 3:127,379,547 | G/A | — | uncertain significance |
| rs759498460 | 3:127,379,560 | C/T | — | uncertain significance |
| rs1354091216 | 3:127,379,619 | C/G | — | uncertain significance |
| rs781757410 | 3:127,379,626 | C/T | — | uncertain significance |
| rs1174827254 | 3:127,379,664 | G/T | — | uncertain significance |
| rs1357045242 | 3:127,379,665 | C/T | — | uncertain significance |
| rs2473361178 | 3:127,379,685 | G/T | — | uncertain significance |
| rs2074762845 | 3:127,379,710 | A/C | — | uncertain significance |
| rs1318090048 | 3:127,379,739 | A/G | — | uncertain significance |
| rs2473361333 | 3:127,379,798 | C/A | — | uncertain significance |
| rs143547670 | 3:127,379,832 | C/G | — | uncertain significance |
| rs2473361394 | 3:127,379,848 | T/C | — | uncertain significance |
| rs2473361471 | 3:127,379,881 | C/G | — | uncertain significance |
| rs1453318935 | 3:127,379,889 | G/A | — | uncertain significance |
| rs754339091 | 3:127,379,922 | G/A | — | uncertain significance |
| rs148570678 | 3:127,379,941 | A/G | — | uncertain significance |
| rs970344851 | 3:127,379,944 | A/G | — | uncertain significance |
| rs34980487 | 3:127,379,948 | C/T | — | likely benign |
| rs774925392 | 3:127,379,956 | G/A | — | uncertain significance |
| rs747169758 | 3:127,387,986 | G/A | — | uncertain significance |
| rs7634281 | 3:127,388,517 | G/C | — | — |
| rs1202141450 | 3:127,390,301 | A/G | — | uncertain significance |
| rs2473374574 | 3:127,390,316 | G/C | — | uncertain significance |
| rs969859253 | 3:127,390,334 | C/G | — | uncertain significance |
| rs2473374722 | 3:127,390,349 | A/G | — | uncertain significance |
| rs748147701 | 3:127,390,358 | G/A | — | uncertain significance |
| rs759288912 | 3:127,390,454 | G/A | — | uncertain significance |
| rs41266485 | 3:127,390,525 | C/T | upstream gene variant | — |
| rs752815181 | 3:127,391,117 | G/A | — | uncertain significance |
| rs2074853067 | 3:127,391,130 | G/A | — | uncertain significance |
| rs2473377317 | 3:127,391,154 | A/T | — | uncertain significance |
| rs2074854264 | 3:127,391,197 | G/T | — | uncertain significance |
| rs1316318028 | 3:127,391,200 | G/C | — | uncertain significance |
| rs757073772 | 3:127,391,210 | C/T | — | uncertain significance |
| rs2473377558 | 3:127,391,215 | C/G | — | uncertain significance |
| rs1052316528 | 3:127,391,268 | G/C | — | uncertain significance |
| rs1490753571 | 3:127,391,270 | G/A | — | uncertain significance |
| rs1199162982 | 3:127,391,271 | G/A | — | uncertain significance |
| rs949249636 | 3:127,391,287 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.