ART3
ADP-ribosyltransferase 3 (inactive)
Summary
This gene encodes an arginine-specific ADP-ribosyltransferase. The encoded protein catalyzes a reversible reaction which modifies proteins by the addition or removal of ADP-ribose to an arginine residue to regulate the function of the modified protein. An ADP-ribosyltransferase pseudogene is located on chromosome 11. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs8878 | 4:76,942,300 | A/C | — | — |
| rs35795399 | 4:76,942,677 | T/C | intron variant | — |
| rs3921 | 4:76,942,943 | C/T | — | — |
| rs56061981 | 4:76,944,785 | C/T | regulatory region variant | — |
| rs4256246 | 4:76,945,522 | G/A | upstream gene variant | — |
| rs4508917 | 4:76,946,097 | A/G | upstream gene variant | — |
| rs4386624 | 4:76,946,139 | G/T | — | — |
| rs56316945 | 4:76,946,589 | A/G | upstream gene variant | — |
| rs4859589 | 4:76,948,299 | A/G | upstream gene variant | — |
| rs6856958 | 4:76,952,356 | T/G | downstream gene variant | — |
| rs4356932 | 4:76,955,194 | T/A | — | — |
| rs4619915 | 4:76,955,201 | A/G | downstream gene variant | — |
| rs61757197 | 4:76,955,947 | T/A | stop lost | — |
| rs6817952 | 4:76,957,043 | G/A | downstream gene variant | — |
| rs190426994 | 4:76,959,984 | G/A | upstream gene variant | — |
| rs12509255 | 4:76,961,994 | C/G | upstream gene variant | — |
| rs35170645 | 4:76,964,956 | A/G | upstream gene variant | — |
| rs558666152 | 4:76,971,550 | A/G | — | — |
| rs142589967 | 4:76,972,752 | G/A | regulatory region variant | — |
| rs143764335 | 4:76,986,825 | T/C | intron variant | — |
| rs35353995 | 4:76,988,000 | T/C | intron variant | — |
| rs146388903 | 4:76,992,852 | A/G | upstream gene variant | — |
| rs192638090 | 4:76,993,095 | G/C | upstream gene variant | — |
| rs761582129 | 4:76,997,058 | T/C | — | uncertain significance |
| rs2477384665 | 4:76,997,062 | A/C | — | uncertain significance |
| rs776853474 | 4:76,997,082 | G/T | — | uncertain significance |
| rs571288797 | 4:76,999,262 | A/G | — | — |
| rs199525110 | 4:77,003,070 | C/A | — | uncertain significance |
| rs1722572199 | 4:77,003,093 | C/G | — | uncertain significance |
| rs142400782 | 4:77,003,203 | T/A | — | uncertain significance |
| rs779445420 | 4:77,003,260 | C/T | — | uncertain significance |
| rs373658035 | 4:77,003,306 | C/G | — | uncertain significance |
| rs750400896 | 4:77,003,309 | G/T | — | uncertain significance |
| rs375657911 | 4:77,003,321 | C/G | — | uncertain significance |
| rs560213585 | 4:77,003,326 | T/A | — | uncertain significance |
| rs138071641 | 4:77,003,361 | C/A | — | uncertain significance |
| rs552301948 | 4:77,003,428 | G/A | — | uncertain significance |
| rs1259270795 | 4:77,003,467 | A/G | — | uncertain significance |
| rs142545952 | 4:77,003,484 | G/A | — | uncertain significance |
| rs145977750 | 4:77,003,520 | A/C | — | uncertain significance |
| rs781058769 | 4:77,003,631 | C/T | — | uncertain significance |
| rs4859612 | 4:77,005,814 | T/G | intron variant | — |
| rs55680121 | 4:77,007,532 | A/G | intron variant | — |
| rs11097230 | 4:77,015,665 | A/G | upstream gene variant | — |
| rs554178231 | 4:77,016,770 | A/C | — | — |
| rs4440243 | 4:77,017,680 | C/T | downstream gene variant | — |
| rs149862377 | 4:77,021,468 | A/G | — | uncertain significance |
| rs145856579 | 4:77,021,968 | G/C | — | uncertain significance |
| rs763549230 | 4:77,021,973 | C/A | — | uncertain significance |
| rs140110202 | 4:77,022,143 | G/A | — | uncertain significance |
| rs750160815 | 4:77,022,155 | A/G | — | uncertain significance |
| rs17001385 | 4:77,022,286 | C/G | intron variant | — |
| rs12331871 | 4:77,023,499 | T/G | intron variant | — |
| rs10033843 | 4:77,028,783 | G/A | intron variant | — |
| rs141288423 | 4:77,029,277 | A/G | intron variant | — |
| rs6836703 | 4:77,030,147 | G/A | intron variant | — |
| rs4416502 | 4:77,030,872 | G/A | downstream gene variant | — |
| rs28592918 | 4:77,032,883 | C/T | downstream gene variant | — |
| rs563799075 | 4:77,033,551 | T/C | — | uncertain significance |
| rs780283755 | 4:77,033,647 | C/A | — | uncertain significance |
| rs14773 | 4:77,033,725 | C/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.