TRHDE
thyrotropin releasing hormone degrading enzyme
Summary
This gene encodes a member of the peptidase M1 family. The encoded protein is an extracellular peptidase that specifically cleaves and inactivates the neuropeptide thyrotropin-releasing hormone.[provided by RefSeq, Dec 2008]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs571745949 | 12:72,559,431 | A/C | — | — |
| rs59211589 | 12:72,648,499 | T/C | coding sequence variant | — |
| rs770248867 | 12:72,666,611 | C/T | — | uncertain significance |
| rs1324548701 | 12:72,666,749 | G/T | — | uncertain significance |
| rs778163030 | 12:72,666,764 | G/A | — | uncertain significance |
| rs377578405 | 12:72,666,770 | G/T | — | uncertain significance |
| rs1332394880 | 12:72,666,911 | G/A | — | uncertain significance |
| rs776708481 | 12:72,666,917 | C/A | — | uncertain significance |
| rs1428709885 | 12:72,667,031 | T/C | — | uncertain significance |
| rs9651989 | 12:72,667,056 | G/A | — | benign |
| rs1481010477 | 12:72,667,108 | G/A | — | uncertain significance |
| rs763296032 | 12:72,667,115 | G/T | — | uncertain significance |
| rs187142374 | 12:72,667,241 | A/G | — | uncertain significance |
| rs144507471 | 12:72,667,286 | A/C | — | uncertain significance |
| rs770620065 | 12:72,667,326 | C/G | — | uncertain significance |
| rs368667547 | 12:72,667,327 | G/T | — | uncertain significance |
| rs2499198971 | 12:72,680,660 | A/C | — | uncertain significance |
| rs1261571869 | 12:72,680,731 | T/G | — | likely benign |
| rs543863390 | 12:72,716,729 | G/A | — | — |
| rs12831974 | 12:72,724,034 | T/A | — | — |
| rs7955732 | 12:72,724,995 | G/T | intron variant | — |
| rs12821309 | 12:72,726,632 | C/G | intron variant | — |
| rs4277154 | 12:72,727,074 | G/C | — | — |
| rs3858590 | 12:72,727,718 | G/A | intron variant | — |
| rs4402340 | 12:72,728,383 | C/A | intron variant | — |
| rs4281517 | 12:72,730,292 | T/C | intron variant | — |
| rs4388934 | 12:72,730,503 | A/G | intron variant | — |
| rs12828944 | 12:72,736,310 | G/A | intron variant | — |
| rs754618894 | 12:72,771,874 | A/G | — | uncertain significance |
| rs1338299684 | 12:72,866,871 | G/A | — | uncertain significance |
| rs893229287 | 12:72,866,907 | G/T | — | uncertain significance |
| rs752918086 | 12:72,866,938 | A/G | — | uncertain significance |
| rs1165179072 | 12:72,866,959 | T/C | — | uncertain significance |
| rs150205223 | 12:72,956,805 | A/G | — | uncertain significance |
| rs1238419477 | 12:72,969,049 | A/G | — | uncertain significance |
| rs796052150 | 12:72,969,085 | A/T | — | likely benign |
| rs138433001 | 12:72,969,157 | C/T | — | uncertain significance |
| rs754941910 | 12:73,012,792 | C/T | — | uncertain significance |
| rs1052400108 | 12:73,012,793 | G/A | — | uncertain significance |
| rs112818045 | 12:73,014,884 | T/C | — | benign |
| rs755535173 | 12:73,015,432 | G/A | — | uncertain significance |
| rs150615630 | 12:73,046,129 | A/C | — | benign |
| rs1156787815 | 12:73,046,816 | A/G | — | uncertain significance |
| rs201517251 | 12:73,046,930 | A/G | — | uncertain significance |
| rs750290595 | 12:73,056,844 | A/T | — | uncertain significance |
| rs1275331109 | 12:73,056,904 | G/C | — | uncertain significance |
| rs745929445 | 12:73,056,913 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.