GOLIM4
golgi integral membrane protein 4
Summary
The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. The protein encoded by this gene is a type II Golgi-resident protein. It may process proteins synthesized in the rough endoplasmic reticulum and assist in the transport of protein cargo through the Golgi apparatus. [provided by RefSeq, Jul 2008]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs542482925 | 3:167,728,142 | C/T | — | uncertain significance |
| rs200359669 | 3:167,728,155 | G/A | — | uncertain significance |
| rs113156663 | 3:167,735,002 | G/A | intron variant | — |
| rs201418456 | 3:167,742,747 | T/C | — | uncertain significance |
| rs139790324 | 3:167,742,756 | T/C | — | uncertain significance |
| rs767544798 | 3:167,742,757 | T/G | — | uncertain significance |
| rs546884426 | 3:167,742,811 | C/T | — | uncertain significance |
| rs774756322 | 3:167,742,870 | T/A | — | uncertain significance |
| rs1718077997 | 3:167,745,548 | G/A | — | uncertain significance |
| rs2473533409 | 3:167,745,598 | T/C | — | uncertain significance |
| rs368126514 | 3:167,745,602 | G/C | — | uncertain significance |
| rs73878613 | 3:167,745,630 | C/A | — | benign |
| rs2473537011 | 3:167,747,067 | A/G | — | uncertain significance |
| rs1718178558 | 3:167,747,086 | G/C | — | uncertain significance |
| rs140959669 | 3:167,747,589 | G/A | — | uncertain significance |
| rs144800331 | 3:167,747,593 | G/A | — | uncertain significance |
| rs61743912 | 3:167,747,643 | T/C | — | benign |
| rs137904787 | 3:167,747,679 | C/A | — | uncertain significance |
| rs116300276 | 3:167,747,829 | G/A | — | benign |
| rs2473544322 | 3:167,750,312 | G/T | — | uncertain significance |
| rs137967362 | 3:167,750,317 | C/T | — | likely benign |
| rs142340864 | 3:167,750,318 | G/A | — | uncertain significance |
| rs373403395 | 3:167,750,319 | C/T | — | uncertain significance |
| rs770165297 | 3:167,750,346 | C/T | — | uncertain significance |
| rs150862007 | 3:167,750,348 | C/T | — | uncertain significance |
| rs756385472 | 3:167,750,375 | C/T | — | uncertain significance |
| rs146509699 | 3:167,750,423 | G/A | — | uncertain significance |
| rs773509036 | 3:167,750,424 | C/T | — | uncertain significance |
| rs935283606 | 3:167,750,526 | G/A | — | uncertain significance |
| rs2473545631 | 3:167,750,595 | C/T | — | uncertain significance |
| rs776942605 | 3:167,750,615 | T/C | — | uncertain significance |
| rs146720058 | 3:167,750,633 | C/T | — | uncertain significance |
| rs371901596 | 3:167,754,661 | T/C | — | likely benign |
| rs148889836 | 3:167,754,775 | A/G | — | uncertain significance |
| rs896299897 | 3:167,758,579 | C/T | — | uncertain significance |
| rs140673913 | 3:167,759,185 | C/G | — | uncertain significance |
| rs931141621 | 3:167,759,242 | C/T | — | uncertain significance |
| rs144070059 | 3:167,761,233 | T/C | — | uncertain significance |
| rs142833364 | 3:167,761,238 | G/A | — | uncertain significance |
| rs567748650 | 3:167,766,082 | C/G | — | uncertain significance |
| rs9813779 | 3:167,789,156 | T/C | intron variant | — |
| rs2473663670 | 3:167,812,977 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.