ALLC
allantoicase
Summary
Allantoicase (EC 3.5.3.4) participates in the uric acid degradation pathway. Its enzymatic activity, like that of urate oxidase (MIM 191540), was lost during vertebrate evolution.[supplied by OMIM, Nov 2008]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs387907076 | 2:3,691,502 | G/A | missense variant | pathogenic |
| rs7567833 | 2:3,691,548 | A/G | missense variant | benign |
| rs201143466 | 2:3,692,238 | C/G | downstream gene variant | — |
| rs369154044 | 2:3,718,766 | T/A | — | uncertain significance |
| rs758297888 | 2:3,718,773 | G/C | — | uncertain significance |
| rs11123610 | 2:3,723,026 | G/A | intron variant | — |
| rs540280415 | 2:3,726,068 | C/G | — | uncertain significance |
| rs764315712 | 2:3,726,070 | T/C | — | uncertain significance |
| rs199666164 | 2:3,727,503 | C/T | — | uncertain significance |
| rs201007073 | 2:3,727,525 | C/G | — | uncertain significance |
| rs374153308 | 2:3,727,570 | C/A | — | uncertain significance |
| rs1667184967 | 2:3,729,297 | T/G | — | uncertain significance |
| rs764588725 | 2:3,730,589 | C/G | — | uncertain significance |
| rs757890281 | 2:3,730,620 | A/G | — | uncertain significance |
| rs1594318 | 2:3,733,944 | C/A | — | — |
| rs780830343 | 2:3,743,308 | T/A | — | uncertain significance |
| rs779592249 | 2:3,743,337 | G/T | — | uncertain significance |
| rs563354282 | 2:3,743,405 | G/A | — | uncertain significance |
| rs762868301 | 2:3,743,918 | G/T | — | uncertain significance |
| rs200233346 | 2:3,743,921 | C/T | — | uncertain significance |
| rs377253960 | 2:3,743,922 | G/A | — | uncertain significance |
| rs1667672424 | 2:3,743,934 | T/C | — | uncertain significance |
| rs770809478 | 2:3,744,946 | G/C | — | likely benign |
| rs35124934 | 2:3,744,990 | G/A | — | benign |
| rs2528632760 | 2:3,745,000 | T/A | — | uncertain significance |
| rs12615970 | 2:3,745,215 | A/T | — | — |
| rs6730148 | 2:3,748,971 | T/C | upstream gene variant | — |
| rs6730396 | 2:3,749,119 | T/C | — | benign |
| rs747021694 | 2:3,749,189 | C/T | — | uncertain significance |
| rs376204543 | 2:3,749,206 | C/G | — | uncertain significance |
| rs369317175 | 2:3,749,230 | C/T | — | likely benign |
| rs756879453 | 2:3,749,989 | A/T | — | uncertain significance |
| rs371997299 | 2:3,750,031 | A/G | — | uncertain significance |
| rs913682533 | 2:3,750,098 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.