MXRA8
matrix remodeling associated 8
Summary
Predicted to be involved in establishment of glial blood-brain barrier. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1557680149 | 1:1,288,995 | T/C | — | uncertain significance |
| rs754362980 | 1:1,289,006 | A/G | — | uncertain significance |
| rs371661982 | 1:1,289,262 | G/T | — | uncertain significance |
| rs148662269 | 1:1,289,283 | C/T | — | likely benign |
| rs374879755 | 1:1,289,293 | A/T | missense variant | pathogenic |
| rs531558101 | 1:1,289,413 | G/T | — | uncertain significance |
| rs150058708 | 1:1,289,446 | C/T | — | likely benign |
| rs1423681920 | 1:1,289,469 | G/A | — | uncertain significance |
| rs1453960689 | 1:1,289,574 | C/T | — | uncertain significance |
| rs147789434 | 1:1,289,818 | G/T | — | uncertain significance |
| rs141809370 | 1:1,289,863 | C/A | — | benign |
| rs201290201 | 1:1,289,865 | T/C | — | likely benign |
| rs61730211 | 1:1,289,874 | C/A | — | uncertain significance |
| rs199522385 | 1:1,289,894 | G/A | — | likely benign |
| rs533557025 | 1:1,290,066 | G/C | — | likely benign |
| rs112004810 | 1:1,290,071 | G/C | — | uncertain significance |
| rs2523285058 | 1:1,290,092 | C/G | — | uncertain significance |
| rs1328715526 | 1:1,290,105 | G/T | — | likely benign |
| rs138606719 | 1:1,290,171 | G/T | — | likely benign |
| rs750276776 | 1:1,290,301 | A/G | — | likely benign |
| rs781461842 | 1:1,290,338 | G/A | — | uncertain significance |
| rs147996767 | 1:1,290,408 | A/G | — | benign |
| rs2523289240 | 1:1,290,478 | C/G | — | uncertain significance |
| rs1569788045 | 1:1,290,496 | T/A | — | uncertain significance |
| rs1429712955 | 1:1,290,500 | T/C | — | uncertain significance |
| rs770790553 | 1:1,290,506 | C/A | — | uncertain significance |
| rs1315688242 | 1:1,290,642 | G/T | — | uncertain significance |
| rs368317360 | 1:1,290,651 | C/T | — | uncertain significance |
| rs142988174 | 1:1,290,664 | G/C | — | likely benign |
| rs375568751 | 1:1,290,695 | G/C | — | uncertain significance |
| rs144784794 | 1:1,290,708 | C/T | — | uncertain significance |
| rs1197100511 | 1:1,290,912 | G/A | — | likely benign |
| rs200138692 | 1:1,290,917 | G/C | missense variant | — |
| rs758043292 | 1:1,290,932 | A/T | — | uncertain significance |
| rs900313866 | 1:1,290,950 | G/A | — | uncertain significance |
| rs1031977795 | 1:1,290,971 | C/G | — | uncertain significance |
| rs954835307 | 1:1,291,036 | G/C | — | uncertain significance |
| rs935417579 | 1:1,291,057 | G/A | — | uncertain significance |
| rs1053984167 | 1:1,291,058 | C/A | — | uncertain significance |
| rs900408652 | 1:1,291,084 | G/A | — | uncertain significance |
| rs181929025 | 1:1,291,085 | C/T | — | benign |
| rs1644112952 | 1:1,291,123 | A/T | — | uncertain significance |
| rs1265724290 | 1:1,292,070 | G/C | — | uncertain significance |
| rs574102381 | 1:1,293,880 | G/A | — | uncertain significance |
| rs4970439 | 1:1,298,411 | C/G | — | — |
| rs28368296 | 1:1,299,366 | C/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.