PRTG
protogenin
Summary
This gene encodes a member of the immunoglobulin superfamily. The encoded transmembrane protein has been associated with the development of various tissues, especially neurogenesis. It has been suggested that this gene may be associated with attention deficit hyperactivity disorder (ADHD). [provided by RefSeq, Nov 2014]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1477329129 | 15:55,903,921 | G/A | — | — |
| rs79244725 | 15:55,912,391 | G/A | — | uncertain significance |
| rs374175748 | 15:55,912,929 | T/C | — | uncertain significance |
| rs1046079450 | 15:55,916,569 | T/C | — | uncertain significance |
| rs372160915 | 15:55,916,572 | T/C | — | uncertain significance |
| rs375437286 | 15:55,916,584 | A/T | — | uncertain significance |
| rs1041501697 | 15:55,916,675 | A/T | — | uncertain significance |
| rs1435354528 | 15:55,919,222 | A/C | — | uncertain significance |
| rs752927785 | 15:55,919,240 | A/C | — | uncertain significance |
| rs758849100 | 15:55,919,305 | A/T | — | uncertain significance |
| rs77440317 | 15:55,921,043 | C/T | missense variant | — |
| rs775016636 | 15:55,921,202 | C/G | — | uncertain significance |
| rs372543315 | 15:55,929,374 | G/A | — | uncertain significance |
| rs371729881 | 15:55,929,521 | C/G | — | uncertain significance |
| rs780955691 | 15:55,930,771 | C/T | — | uncertain significance |
| rs201846185 | 15:55,930,816 | C/T | — | uncertain significance |
| rs373584731 | 15:55,931,963 | G/A | — | uncertain significance |
| rs779696205 | 15:55,931,996 | G/C | — | uncertain significance |
| rs781140561 | 15:55,932,012 | T/C | — | uncertain significance |
| rs200167052 | 15:55,932,014 | C/G | — | uncertain significance |
| rs374530620 | 15:55,933,358 | T/A | — | uncertain significance |
| rs368774482 | 15:55,933,359 | C/A | — | uncertain significance |
| rs747248788 | 15:55,933,361 | A/G | — | uncertain significance |
| rs371274747 | 15:55,933,380 | G/A | — | uncertain significance |
| rs117321578 | 15:55,942,236 | T/G | intron variant | — |
| rs189343264 | 15:55,948,165 | A/T | intron variant | — |
| rs11071200 | 15:55,950,082 | C/A | intron variant | — |
| rs775874509 | 15:55,964,657 | G/A | — | uncertain significance |
| rs757236112 | 15:55,964,751 | T/C | — | uncertain significance |
| rs1207967557 | 15:55,964,768 | T/A | — | uncertain significance |
| rs149494002 | 15:55,964,778 | C/G | — | benign |
| rs1442080719 | 15:55,965,656 | C/T | — | uncertain significance |
| rs75403514 | 15:55,965,666 | A/G | — | benign |
| rs369543420 | 15:55,965,731 | T/C | — | uncertain significance |
| rs2141798346 | 15:55,965,799 | G/C | — | uncertain significance |
| rs2542722259 | 15:55,965,853 | A/T | — | uncertain significance |
| rs140985611 | 15:55,967,649 | T/G | upstream gene variant | — |
| rs1249980910 | 15:55,967,733 | C/G | — | uncertain significance |
| rs201067183 | 15:55,967,741 | C/A | — | uncertain significance |
| rs1054276863 | 15:55,967,786 | T/C | — | uncertain significance |
| rs1567095300 | 15:55,970,033 | T/C | — | uncertain significance |
| rs371560935 | 15:55,970,232 | T/C | — | uncertain significance |
| rs202160989 | 15:55,970,235 | C/T | — | uncertain significance |
| rs757293203 | 15:55,971,515 | G/A | — | uncertain significance |
| rs200938799 | 15:55,971,561 | T/G | — | likely benign |
| rs773260004 | 15:55,971,598 | C/T | — | uncertain significance |
| rs186873190 | 15:55,972,381 | G/A | — | uncertain significance |
| rs368752238 | 15:55,972,788 | C/T | — | uncertain significance |
| rs755126845 | 15:55,974,579 | G/A | — | uncertain significance |
| rs371167586 | 15:55,974,600 | C/T | — | uncertain significance |
| rs769696696 | 15:55,976,012 | C/T | — | uncertain significance |
| rs750722793 | 15:55,976,045 | T/C | — | uncertain significance |
| rs1372142654 | 15:55,976,051 | G/A | — | uncertain significance |
| rs2542750074 | 15:55,976,082 | C/T | — | uncertain significance |
| rs868147000 | 15:55,976,091 | C/T | — | uncertain significance |
| rs200495272 | 15:55,976,103 | T/C | — | likely benign |
| rs12912118 | 15:56,022,928 | G/T | intron variant | — |
| rs192038672 | 15:56,029,487 | A/G | regulatory region variant | — |
| rs768743389 | 15:56,032,641 | C/A | — | uncertain significance |
| rs2031578295 | 15:56,032,798 | C/A | — | uncertain significance |
| rs2542859605 | 15:56,032,825 | G/A | — | uncertain significance |
| rs772552811 | 15:56,032,829 | C/A | — | uncertain significance |
| rs1230160672 | 15:56,032,835 | C/G | — | uncertain significance |
| rs35718474 | 15:56,035,093 | G/A | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.