SLCO3A1
solute carrier organic anion transporter family member 3A1
Summary
Enables organic anion transmembrane transporter activity and prostaglandin transmembrane transporter activity. Involved in positive regulation of MAPK cascade; positive regulation of canonical NF-kappaB signal transduction; and prostaglandin transport. Located in basal plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs60495981 | 15:92,420,515 | T/G | intron variant | — |
| rs56880057 | 15:92,420,632 | C/G | intron variant | — |
| rs72750054 | 15:92,421,696 | C/T | intron variant | — |
| rs56277940 | 15:92,424,424 | G/T | intron variant | — |
| rs72750059 | 15:92,428,107 | C/T | — | — |
| rs75517863 | 15:92,428,786 | T/G | — | — |
| rs7173089 | 15:92,438,457 | C/T | regulatory region variant | — |
| rs72750064 | 15:92,439,235 | C/T | intron variant | — |
| rs72750065 | 15:92,441,169 | G/A | intron variant | — |
| rs55767000 | 15:92,443,856 | G/A | intron variant | — |
| rs56292826 | 15:92,443,866 | A/G | — | — |
| rs72750075 | 15:92,444,871 | T/C | intron variant | — |
| rs3924426 | 15:92,445,873 | T/C | intron variant | — |
| rs55772252 | 15:92,447,710 | T/C | intron variant | — |
| rs72750081 | 15:92,448,712 | G/T | — | — |
| rs61742322 | 15:92,451,905 | C/G | regulatory region variant | — |
| rs752631809 | 15:92,459,506 | C/T | — | uncertain significance |
| rs756275514 | 15:92,459,514 | G/T | — | uncertain significance |
| rs772434157 | 15:92,459,529 | C/A | — | uncertain significance |
| rs1393895006 | 15:92,459,560 | C/T | — | uncertain significance |
| rs7495052 | 15:92,552,029 | T/A | — | — |
| rs11854488 | 15:92,572,509 | G/C | intron variant | — |
| rs72757415 | 15:92,572,762 | G/T | intron variant | — |
| rs7498044 | 15:92,573,639 | G/A | intron variant | — |
| rs12899055 | 15:92,604,530 | C/T | — | association |
| rs34555786 | 15:92,611,169 | G/A | intron variant | — |
| rs753830023 | 15:92,647,606 | G/C | — | uncertain significance |
| rs1517618 | 15:92,647,645 | G/A | synonymous variant | — |
| rs367922921 | 15:92,647,649 | G/A | — | uncertain significance |
| rs751987219 | 15:92,647,726 | C/A | — | uncertain significance |
| rs207959 | 15:92,655,262 | T/C | intron variant | — |
| rs207954 | 15:92,657,373 | T/G | — | — |
| rs1567130598 | 15:92,663,740 | C/T | — | uncertain significance |
| rs376389355 | 15:92,669,338 | C/T | — | uncertain significance |
| rs776746205 | 15:92,669,477 | C/A | — | uncertain significance |
| rs117100186 | 15:92,671,587 | A/G | — | likely benign |
| rs1453308836 | 15:92,671,693 | G/C | — | uncertain significance |
| rs888799439 | 15:92,679,898 | T/G | — | — |
| rs2238355 | 15:92,685,778 | T/C | intron variant | — |
| rs752852634 | 15:92,690,221 | C/T | — | uncertain significance |
| rs774117751 | 15:92,690,255 | G/C | — | uncertain significance |
| rs766437983 | 15:92,690,265 | G/A | — | uncertain significance |
| rs141187463 | 15:92,690,379 | A/G | — | likely benign |
| rs75366367 | 15:92,694,174 | A/G | — | benign |
| rs2505734850 | 15:92,694,212 | T/G | — | uncertain significance |
| rs2238341 | 15:92,705,031 | A/T | — | — |
| rs2505751954 | 15:92,705,998 | C/T | — | uncertain significance |
| rs201801796 | 15:92,706,063 | C/A | — | uncertain significance |
| rs199888371 | 15:92,706,064 | A/G | — | uncertain significance |
| rs764695708 | 15:92,706,093 | G/A | — | uncertain significance |
| rs201208000 | 15:92,706,127 | C/T | — | uncertain significance |
| rs935299180 | 15:92,706,144 | T/G | — | uncertain significance |
| rs200441873 | 15:92,706,192 | C/T | — | uncertain significance |
| rs777771745 | 15:92,706,209 | C/G | — | uncertain significance |
| rs2505763124 | 15:92,715,087 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.