PTPRZ1
protein tyrosine phosphatase receptor type Z1
Summary
This gene encodes a member of the receptor protein tyrosine phosphatase family. Expression of this gene is restricted to the central nervous system (CNS), and it may be involved in the regulation of specific developmental processes in the CNS. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2011]
Known Variants118 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs145620191 | 7:121,584,426 | G/C | intron variant | — |
| rs761886073 | 7:121,608,109 | C/T | — | uncertain significance |
| rs143196687 | 7:121,608,118 | C/A | — | uncertain significance |
| rs141251052 | 7:121,612,648 | G/A | — | uncertain significance |
| rs137935426 | 7:121,616,249 | C/T | — | uncertain significance |
| rs1257076255 | 7:121,616,274 | A/C | — | uncertain significance |
| rs145928149 | 7:121,616,320 | G/A | — | uncertain significance |
| rs753434326 | 7:121,616,331 | T/C | — | likely benign |
| rs139790820 | 7:121,616,845 | A/G | — | uncertain significance |
| rs1455886533 | 7:121,616,887 | G/A | — | uncertain significance |
| rs483352722 | 7:121,623,762 | G/T | — | uncertain significance |
| rs1465851099 | 7:121,624,071 | G/A | — | uncertain significance |
| rs143965756 | 7:121,624,122 | T/C | — | benign |
| rs202215379 | 7:121,636,450 | C/G | — | uncertain significance |
| rs370195659 | 7:121,636,532 | T/C | — | uncertain significance |
| rs372276831 | 7:121,636,546 | G/A | — | uncertain significance |
| rs146755280 | 7:121,636,589 | A/G | — | uncertain significance |
| rs144723430 | 7:121,636,605 | T/C | — | likely benign |
| rs761886146 | 7:121,637,947 | A/G | — | uncertain significance |
| rs200342007 | 7:121,638,039 | G/A | — | uncertain significance |
| rs372571641 | 7:121,644,671 | T/A | — | uncertain significance |
| rs2485773079 | 7:121,650,415 | G/C | — | uncertain significance |
| rs143548439 | 7:121,650,488 | C/T | — | uncertain significance |
| rs185158958 | 7:121,650,506 | G/A | — | uncertain significance |
| rs369032550 | 7:121,650,542 | G/A | — | uncertain significance |
| rs373965772 | 7:121,650,550 | A/G | — | uncertain significance |
| rs1428557586 | 7:121,650,593 | C/T | — | uncertain significance |
| rs150062891 | 7:121,650,770 | C/T | — | likely benign |
| rs573635033 | 7:121,650,784 | A/G | — | uncertain significance |
| rs755532836 | 7:121,650,793 | A/G | — | uncertain significance |
| rs376891530 | 7:121,650,835 | C/T | — | uncertain significance |
| rs747760131 | 7:121,650,836 | T/C | — | uncertain significance |
| rs140937221 | 7:121,650,872 | C/G | — | uncertain significance |
| rs375597072 | 7:121,650,874 | G/A | — | uncertain significance |
| rs144692047 | 7:121,650,917 | G/A | — | uncertain significance |
| rs746624870 | 7:121,651,042 | A/G | — | likely benign |
| rs946800806 | 7:121,651,082 | C/G | — | uncertain significance |
| rs10229870 | 7:121,651,221 | T/C | — | benign |
| rs756721096 | 7:121,651,265 | A/C | — | uncertain significance |
| rs2485778892 | 7:121,651,276 | C/T | — | uncertain significance |
| rs965287885 | 7:121,651,327 | G/A | — | uncertain significance |
| rs1022501537 | 7:121,651,391 | G/A | — | uncertain significance |
| rs1339954193 | 7:121,651,405 | C/G | — | uncertain significance |
| rs2485780297 | 7:121,651,493 | C/T | — | uncertain significance |
| rs769107338 | 7:121,651,557 | G/C | — | uncertain significance |
| rs770406556 | 7:121,651,598 | G/A | — | likely benign |
| rs757457460 | 7:121,651,633 | G/C | — | uncertain significance |
| rs756306704 | 7:121,651,648 | G/A | — | uncertain significance |
| rs2485781370 | 7:121,651,690 | G/C | — | uncertain significance |
| rs779280823 | 7:121,651,778 | G/A | — | uncertain significance |
| rs1244523090 | 7:121,651,786 | T/C | — | uncertain significance |
| rs773190017 | 7:121,651,846 | A/G | — | uncertain significance |
| rs776785104 | 7:121,651,951 | C/T | — | uncertain significance |
| rs142021602 | 7:121,651,993 | G/A | — | likely benign |
| rs1202491598 | 7:121,652,021 | C/T | — | uncertain significance |
| rs776426846 | 7:121,652,029 | A/G | — | uncertain significance |
| rs1471242008 | 7:121,652,105 | A/G | — | uncertain significance |
| rs74821923 | 7:121,652,170 | G/C | — | benign |
| rs1798689910 | 7:121,652,241 | A/G | — | likely benign |
| rs2485785201 | 7:121,652,310 | C/G | — | likely benign |
| rs961402009 | 7:121,652,322 | G/A | — | uncertain significance |
| rs76373682 | 7:121,652,338 | C/A | — | benign |
| rs752657525 | 7:121,652,572 | A/G | — | uncertain significance |
| rs764299227 | 7:121,652,584 | T/C | — | uncertain significance |
| rs61732011 | 7:121,652,598 | G/A | — | benign |
| rs553853277 | 7:121,652,599 | C/A | — | uncertain significance |
| rs2485787795 | 7:121,652,777 | T/C | — | likely benign |
| rs1798714399 | 7:121,652,786 | C/A | — | uncertain significance |
| rs766648148 | 7:121,652,947 | G/T | — | uncertain significance |
| rs552232263 | 7:121,652,962 | A/G | — | uncertain significance |
| rs139671030 | 7:121,652,964 | T/C | — | benign |
| rs2485789498 | 7:121,653,050 | T/C | — | uncertain significance |
| rs777808266 | 7:121,653,142 | G/A | — | uncertain significance |
| rs145746316 | 7:121,653,218 | A/T | — | uncertain significance |
| rs61732008 | 7:121,653,226 | A/G | — | uncertain significance |
| rs762524969 | 7:121,653,346 | G/A | — | uncertain significance |
| rs199893308 | 7:121,653,384 | T/G | — | uncertain significance |
| rs1238558021 | 7:121,653,385 | G/A | — | uncertain significance |
| rs2485792210 | 7:121,653,440 | C/T | — | uncertain significance |
| rs375871165 | 7:121,653,466 | A/T | — | uncertain significance |
| rs144360433 | 7:121,653,532 | T/A | — | uncertain significance |
| rs539589616 | 7:121,653,651 | T/G | — | uncertain significance |
| rs746414310 | 7:121,653,667 | G/C | — | uncertain significance |
| rs2485794137 | 7:121,653,769 | G/A | — | uncertain significance |
| rs139218540 | 7:121,653,817 | A/G | — | uncertain significance |
| rs1328140208 | 7:121,653,853 | G/A | — | uncertain significance |
| rs763160827 | 7:121,653,910 | G/A | — | uncertain significance |
| rs1452483552 | 7:121,659,228 | G/A | — | uncertain significance |
| rs778664781 | 7:121,659,233 | C/T | — | likely benign |
| rs201044306 | 7:121,659,304 | G/T | — | uncertain significance |
| rs765548095 | 7:121,668,630 | T/A | — | uncertain significance |
| rs958191976 | 7:121,668,653 | C/G | — | uncertain significance |
| rs368834797 | 7:121,668,665 | C/G | — | uncertain significance |
| rs184288962 | 7:121,671,524 | G/A | — | benign |
| rs1470879668 | 7:121,671,582 | A/G | — | uncertain significance |
| rs148161989 | 7:121,674,150 | C/A | — | uncertain significance |
| rs1246173566 | 7:121,674,387 | C/T | — | uncertain significance |
| rs2485881438 | 7:121,678,855 | A/G | — | uncertain significance |
| rs767723175 | 7:121,678,932 | G/A | — | uncertain significance |
| rs562739807 | 7:121,679,553 | G/A | — | uncertain significance |
Showing 100 of 118 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.