MPDZ
multiple PDZ domain crumbs cell polarity complex component
Summary
The protein encoded by this gene has multiple PDZ domains, which are hallmarks of protein-protein interactions. The encoded protein is known to interact with the HTR2C receptor and may cause it to clump at the cell surface. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]
Known Variants1,445 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs762562059 | 9:13,106,972 | G/A | — | uncertain significance |
| rs193280665 | 9:13,107,001 | C/T | — | likely benign |
| rs745768687 | 9:13,107,002 | G/A | — | uncertain significance |
| rs375734908 | 9:13,107,011 | T/C | — | uncertain significance |
| rs1206280046 | 9:13,107,013 | G/A | — | uncertain significance |
| rs1305570451 | 9:13,107,015 | A/T | — | likely benign |
| rs200404626 | 9:13,107,019 | G/A | — | uncertain significance |
| rs2537477974 | 9:13,107,022 | T/G | — | uncertain significance |
| rs369281280 | 9:13,107,028 | T/C | — | uncertain significance |
| rs1249265232 | 9:13,107,030 | G/T | — | likely benign |
| rs1941573073 | 9:13,107,031 | G/A | — | uncertain significance |
| rs754386365 | 9:13,107,038 | C/T | — | uncertain significance |
| rs760036444 | 9:13,107,046 | C/T | — | uncertain significance |
| rs1432642106 | 9:13,107,048 | C/T | — | likely benign |
| rs765649084 | 9:13,107,050 | G/A | — | uncertain significance |
| rs1369078759 | 9:13,107,055 | T/C | — | uncertain significance |
| rs140627050 | 9:13,107,062 | C/T | — | uncertain significance |
| rs369284040 | 9:13,107,065 | T/C | — | uncertain significance |
| rs2130914626 | 9:13,107,070 | T/G | — | uncertain significance |
| rs745854560 | 9:13,107,074 | C/T | — | uncertain significance |
| rs200049739 | 9:13,107,075 | G/A | — | benign |
| rs2537480950 | 9:13,107,076 | C/T | — | uncertain significance |
| rs1308010726 | 9:13,107,079 | C/G | — | uncertain significance |
| rs749135989 | 9:13,107,083 | T/A | — | uncertain significance |
| rs1802495 | 9:13,107,088 | C/T | — | uncertain significance |
| rs150393677 | 9:13,107,092 | C/T | — | conflicting classifications of pathogenicity |
| rs1019373900 | 9:13,107,095 | C/T | — | uncertain significance |
| rs759555902 | 9:13,107,099 | A/C | — | likely benign |
| rs1586828923 | 9:13,107,102 | G/A | — | likely benign |
| rs2130916169 | 9:13,107,105 | T/C | — | likely benign |
| rs2130916456 | 9:13,107,111 | C/G | — | uncertain significance |
| rs376956306 | 9:13,107,114 | C/A | — | likely benign |
| rs573472055 | 9:13,107,115 | A/G | — | likely benign |
| rs1164552368 | 9:13,107,120 | A/C | — | uncertain significance |
| rs138137628 | 9:13,107,121 | T/C | — | benign |
| rs374788114 | 9:13,107,126 | T/C | — | likely benign |
| rs566586934 | 9:13,107,130 | C/T | — | likely benign |
| rs368503763 | 9:13,108,915 | G/T | — | likely benign |
| rs764573637 | 9:13,108,919 | A/C | — | likely benign |
| rs2537578154 | 9:13,108,923 | T/C | — | likely benign |
| rs2537578317 | 9:13,108,926 | C/T | — | likely benign |
| rs1283437402 | 9:13,108,927 | A/T | — | likely benign |
| rs1941946773 | 9:13,108,941 | A/G | — | likely benign |
| rs371963885 | 9:13,108,946 | C/G | — | uncertain significance |
| rs750045780 | 9:13,108,948 | G/T | — | uncertain significance |
| rs755736030 | 9:13,108,955 | C/T | — | uncertain significance |
| rs1332806177 | 9:13,108,961 | T/C | — | uncertain significance |
| rs1941951275 | 9:13,108,972 | C/A | — | uncertain significance |
| rs185422539 | 9:13,108,984 | C/G | — | uncertain significance |
| rs769926140 | 9:13,108,987 | T/C | — | uncertain significance |
| rs376840314 | 9:13,108,989 | T/C | — | likely benign |
| rs769047907 | 9:13,109,000 | T/C | — | uncertain significance |
| rs1365547819 | 9:13,109,006 | A/C | — | uncertain significance |
| rs369825815 | 9:13,109,019 | T/C | — | likely benign |
| rs767969634 | 9:13,109,026 | C/T | — | uncertain significance |
| rs766044975 | 9:13,109,031 | T/C | — | likely benign |
| rs538619524 | 9:13,109,033 | G/C | — | uncertain significance |
| rs546961898 | 9:13,109,035 | G/C | — | uncertain significance |
| rs754448147 | 9:13,109,039 | T/C | — | uncertain significance |
| rs765428302 | 9:13,109,049 | T/G | — | uncertain significance |
| rs746143069 | 9:13,109,062 | C/T | — | likely benign |
| rs1274294695 | 9:13,109,063 | G/A | — | likely benign |
| rs1216812641 | 9:13,109,069 | G/A | — | likely benign |
| rs751355249 | 9:13,109,942 | T/C | — | likely benign |
| rs757005699 | 9:13,109,943 | G/A | — | likely benign |
| rs1279695234 | 9:13,109,946 | C/T | — | uncertain significance |
| rs2537654037 | 9:13,109,948 | C/G | — | uncertain significance |
| rs779048168 | 9:13,109,952 | C/T | — | uncertain significance |
| rs372873246 | 9:13,109,962 | C/G | — | uncertain significance |
| rs376485985 | 9:13,109,963 | T/A | — | uncertain significance |
| rs201230061 | 9:13,109,969 | A/G | — | uncertain significance |
| rs747413277 | 9:13,109,974 | G/A | — | likely benign |
| rs1205455000 | 9:13,109,980 | C/T | — | likely benign |
| rs981939723 | 9:13,109,981 | G/A | — | uncertain significance |
| rs73404389 | 9:13,110,000 | G/A | — | uncertain significance |
| rs1942168376 | 9:13,110,002 | C/G | — | uncertain significance |
| rs761562072 | 9:13,110,012 | C/T | — | uncertain significance |
| rs767309717 | 9:13,110,016 | C/T | — | likely benign |
| rs1474340356 | 9:13,110,018 | C/T | — | uncertain significance |
| rs2537661157 | 9:13,110,025 | A/G | — | likely benign |
| rs1305802982 | 9:13,110,031 | T/C | — | likely benign |
| rs758517075 | 9:13,110,045 | C/T | — | uncertain significance |
| rs1942177012 | 9:13,110,053 | C/G | — | uncertain significance |
| rs771243192 | 9:13,110,060 | C/T | — | uncertain significance |
| rs376000436 | 9:13,110,061 | C/G | — | likely benign |
| rs2537664256 | 9:13,110,062 | A/G | — | uncertain significance |
| rs143773952 | 9:13,110,066 | G/A | — | likely benign |
| rs181920384 | 9:13,110,067 | C/T | — | likely benign |
| rs774310674 | 9:13,110,068 | G/A | — | likely benign |
| rs1178252669 | 9:13,110,069 | C/T | — | likely benign |
| rs767275187 | 9:13,110,071 | C/A | — | likely benign |
| rs760320154 | 9:13,110,076 | G/C | — | likely benign |
| rs2537666522 | 9:13,110,077 | G/C | — | likely benign |
| rs765587653 | 9:13,110,080 | G/A | — | likely benign |
| rs766258491 | 9:13,110,619 | G/C | — | likely benign |
| rs1299716023 | 9:13,110,620 | G/C | — | likely benign |
| rs2537703561 | 9:13,110,628 | A/G | — | likely benign |
| rs775898143 | 9:13,110,631 | T/C | — | uncertain significance |
| rs75560250 | 9:13,110,636 | T/A | — | uncertain significance |
| rs1266147740 | 9:13,110,638 | C/T | — | uncertain significance |
Showing 100 of 1,445 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.