ECM2
extracellular matrix protein 2
Summary
ECM2 encodes extracellular matrix protein 2, so named because it shares extensive similarity with known extracelluar matrix proteins. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758206748 | 9:95,258,661 | G/A | — | uncertain significance |
| rs151070730 | 9:95,263,010 | G/A | — | uncertain significance |
| rs2492020126 | 9:95,263,042 | A/C | — | uncertain significance |
| rs140976209 | 9:95,263,058 | G/T | — | uncertain significance |
| rs201745324 | 9:95,263,129 | T/C | — | uncertain significance |
| rs570789332 | 9:95,263,141 | C/T | — | uncertain significance |
| rs141859598 | 9:95,263,155 | A/T | — | uncertain significance |
| rs199600306 | 9:95,263,232 | G/A | — | uncertain significance |
| rs775261362 | 9:95,263,288 | G/A | — | uncertain significance |
| rs753296244 | 9:95,264,840 | T/C | — | uncertain significance |
| rs2492027341 | 9:95,264,867 | A/G | — | uncertain significance |
| rs143859115 | 9:95,264,878 | A/T | — | uncertain significance |
| rs1394575979 | 9:95,264,897 | G/A | — | uncertain significance |
| rs534728316 | 9:95,267,819 | A/G | — | uncertain significance |
| rs769232573 | 9:95,267,840 | G/A | — | uncertain significance |
| rs1188801327 | 9:95,267,867 | A/G | — | uncertain significance |
| rs376333101 | 9:95,267,871 | G/T | — | uncertain significance |
| rs2492037712 | 9:95,267,882 | A/G | — | uncertain significance |
| rs534955473 | 9:95,272,199 | C/T | — | uncertain significance |
| rs376172195 | 9:95,272,204 | G/A | — | uncertain significance |
| rs139215803 | 9:95,272,301 | T/A | — | uncertain significance |
| rs1304538107 | 9:95,274,388 | G/T | — | uncertain significance |
| rs142186054 | 9:95,274,397 | C/T | — | likely benign |
| rs141793116 | 9:95,274,403 | A/G | — | uncertain significance |
| rs201012391 | 9:95,276,951 | G/A | — | uncertain significance |
| rs560017678 | 9:95,277,023 | C/T | — | uncertain significance |
| rs753114560 | 9:95,277,090 | C/T | — | uncertain significance |
| rs747962006 | 9:95,277,102 | C/G | — | uncertain significance |
| rs137929518 | 9:95,277,147 | C/G | — | uncertain significance |
| rs142591312 | 9:95,277,171 | G/A | — | uncertain significance |
| rs781141251 | 9:95,277,191 | C/T | — | uncertain significance |
| rs2492140930 | 9:95,277,200 | T/A | — | uncertain significance |
| rs142198335 | 9:95,277,303 | C/T | — | uncertain significance |
| rs755948443 | 9:95,277,344 | T/C | — | uncertain significance |
| rs149769253 | 9:95,277,407 | G/C | — | uncertain significance |
| rs147912487 | 9:95,277,471 | G/A | — | uncertain significance |
| rs111927950 | 9:95,279,532 | G/C | regulatory region variant | — |
| rs1299948905 | 9:95,279,984 | C/G | — | uncertain significance |
| rs2492177006 | 9:95,280,011 | C/G | — | uncertain significance |
| rs747104624 | 9:95,280,082 | G/A | — | uncertain significance |
| rs184863947 | 9:95,280,708 | G/A | intron variant | — |
| rs72754434 | 9:95,283,708 | G/T | intron variant | — |
| rs2492225961 | 9:95,284,944 | T/C | — | likely benign |
| rs763373947 | 9:95,285,004 | A/T | — | uncertain significance |
| rs766786749 | 9:95,285,005 | T/A | — | uncertain significance |
| rs772784389 | 9:95,285,084 | T/G | — | uncertain significance |
| rs927866 | 9:95,294,311 | A/G | — | — |
| rs79072821 | 9:95,299,149 | A/T | upstream gene variant | — |
| rs13296623 | 9:95,301,627 | T/C | regulatory region variant | — |
| rs112989973 | 9:95,314,381 | A/G | intron variant | — |
| rs7852510 | 9:95,316,359 | T/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.