OLFM4
olfactomedin 4
Summary
This gene was originally cloned from human myeloblasts and found to be selectively expressed in inflammed colonic epithelium. This gene encodes a member of the olfactomedin family. The encoded protein is an antiapoptotic factor that promotes tumor growth and is an extracellular matrix glycoprotein that facilitates cell adhesion. [provided by RefSeq, Mar 2011]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17552047 | 13:53,602,462 | G/A | upstream gene variant | — |
| rs774897874 | 13:53,602,982 | G/A | — | uncertain significance |
| rs145322330 | 13:53,603,035 | T/G | — | uncertain significance |
| rs1421274799 | 13:53,603,041 | G/C | — | uncertain significance |
| rs151240563 | 13:53,603,092 | G/C | — | uncertain significance |
| rs1304781941 | 13:53,603,102 | C/T | — | uncertain significance |
| rs373925038 | 13:53,603,144 | G/A | — | uncertain significance |
| rs750555521 | 13:53,608,501 | G/A | — | uncertain significance |
| rs552556405 | 13:53,608,570 | A/G | — | uncertain significance |
| rs774935269 | 13:53,608,580 | G/A | — | uncertain significance |
| rs776892225 | 13:53,608,610 | A/G | — | uncertain significance |
| rs9568796 | 13:53,609,971 | G/T | — | — |
| rs140154469 | 13:53,611,330 | G/C | intron variant | — |
| rs9568797 | 13:53,613,559 | C/G | — | — |
| rs767153379 | 13:53,616,087 | C/G | — | uncertain significance |
| rs775749551 | 13:53,616,141 | A/G | — | uncertain significance |
| rs756131102 | 13:53,617,291 | A/C | — | uncertain significance |
| rs932555490 | 13:53,617,385 | C/T | — | uncertain significance |
| rs551914148 | 13:53,624,208 | T/C | — | uncertain significance |
| rs1385357449 | 13:53,624,209 | C/T | — | uncertain significance |
| rs778415323 | 13:53,624,364 | A/G | — | uncertain significance |
| rs370452390 | 13:53,624,488 | G/A | — | uncertain significance |
| rs756941149 | 13:53,624,617 | T/C | — | uncertain significance |
| rs772138750 | 13:53,624,676 | A/G | — | uncertain significance |
| rs1298181690 | 13:53,624,778 | A/G | — | uncertain significance |
| rs781324654 | 13:53,624,797 | A/G | — | likely benign |
| rs1954743491 | 13:53,624,819 | C/G | — | uncertain significance |
| rs12552 | 13:53,625,781 | A/G | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.