IDO2
indoleamine 2,3-dioxygenase 2
Summary
Along with the enzymes encoded by the INDO (MIM 147435) and TDO2 (MIM 191070) genes, the enzyme encoded by the INDOL1 gene metabolizes tryptophan in the kynurenine pathway (Ball et al., 2007 [PubMed 17499941]).[supplied by OMIM, Feb 2011]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs561468024 | 8:39,791,147 | A/C | — | — |
| rs1380699261 | 8:39,806,761 | G/C | — | uncertain significance |
| rs780050793 | 8:39,806,766 | C/A | — | uncertain significance |
| rs747084870 | 8:39,806,775 | G/C | — | uncertain significance |
| rs2729456 | 8:39,819,808 | T/G | intron variant | — |
| rs774893539 | 8:39,821,136 | C/T | — | uncertain significance |
| rs2536911722 | 8:39,821,148 | A/G | — | uncertain significance |
| rs750799948 | 8:39,821,170 | A/G | — | uncertain significance |
| rs780286284 | 8:39,821,187 | A/T | — | uncertain significance |
| rs755029260 | 8:39,821,208 | G/C | — | uncertain significance |
| rs73619581 | 8:39,821,219 | C/G | — | uncertain significance |
| rs2160860 | 8:39,823,145 | A/T | intron variant | — |
| rs377075058 | 8:39,836,622 | C/T | — | uncertain significance |
| rs1302610612 | 8:39,836,632 | G/T | — | uncertain significance |
| rs1808304261 | 8:39,836,674 | T/C | — | uncertain significance |
| rs1027051055 | 8:39,840,221 | G/T | — | uncertain significance |
| rs4736794 | 8:39,840,234 | A/G | — | benign |
| rs755830973 | 8:39,840,288 | G/A | — | likely benign |
| rs756920209 | 8:39,843,030 | C/G | — | uncertain significance |
| rs753736351 | 8:39,843,031 | C/A | — | uncertain significance |
| rs200097695 | 8:39,845,403 | A/G | — | uncertain significance |
| rs761428678 | 8:39,845,421 | G/A | — | uncertain significance |
| rs2536937784 | 8:39,845,444 | A/G | — | uncertain significance |
| rs749382557 | 8:39,845,454 | G/T | — | uncertain significance |
| rs757580645 | 8:39,847,330 | A/C | — | uncertain significance |
| rs563984978 | 8:39,847,342 | T/G | — | uncertain significance |
| rs5029660 | 8:39,852,660 | A/C | coding sequence variant | — |
| rs780231883 | 8:39,862,857 | C/A | — | uncertain significance |
| rs112843963 | 8:39,862,861 | A/G | — | uncertain significance |
| rs560515044 | 8:39,862,868 | T/G | — | uncertain significance |
| rs10109853 | 8:39,862,881 | C/T | missense variant | benign |
| rs200354370 | 8:39,871,098 | C/T | — | uncertain significance |
| rs530531915 | 8:39,871,157 | G/A | — | uncertain significance |
| rs1172478780 | 8:39,872,822 | G/A | — | uncertain significance |
| rs1428852466 | 8:39,872,904 | G/A | — | uncertain significance |
| rs1281888727 | 8:39,872,912 | G/A | — | uncertain significance |
| rs4503083 | 8:39,872,935 | T/A | stop gained | benign |
| rs1802374045 | 8:39,873,015 | C/T | — | uncertain significance |
| rs1381206625 | 8:39,873,037 | G/A | — | likely benign |
| rs768492657 | 8:39,873,039 | G/A | — | uncertain significance |
| rs768043479 | 8:39,873,078 | T/C | — | uncertain significance |
| rs768546107 | 8:39,873,113 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.