RGMA
repulsive guidance molecule BMP co-receptor a
Summary
This gene encodes a member of the repulsive guidance molecule family. The encoded protein is a glycosylphosphatidylinositol-anchored glycoprotein that functions as an axon guidance protein in the developing and adult central nervous system. This protein may also function as a tumor suppressor in some cancers. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs768402128 | 15:93,588,259 | G/A | — | likely benign |
| rs574979414 | 15:93,588,263 | C/T | — | likely benign |
| rs372095069 | 15:93,588,283 | C/A | — | uncertain significance |
| rs376138060 | 15:93,588,343 | A/G | — | uncertain significance |
| rs757122259 | 15:93,588,415 | T/C | — | uncertain significance |
| rs986554015 | 15:93,588,523 | T/C | — | uncertain significance |
| rs747372439 | 15:93,588,524 | C/T | — | uncertain significance |
| rs987872237 | 15:93,588,544 | C/A | — | uncertain significance |
| rs772994071 | 15:93,588,611 | G/C | — | uncertain significance |
| rs61733836 | 15:93,588,657 | G/A | — | benign |
| rs746589154 | 15:93,588,827 | C/T | — | uncertain significance |
| rs1239567004 | 15:93,588,833 | C/T | — | uncertain significance |
| rs112623341 | 15:93,588,870 | G/C | — | uncertain significance |
| rs2505685559 | 15:93,588,875 | T/C | — | uncertain significance |
| rs4424872 | 15:93,590,070 | T/A | intron variant | — |
| rs76069502 | 15:93,593,064 | G/A | intron variant | — |
| rs576601683 | 15:93,595,249 | C/T | — | uncertain significance |
| rs754606236 | 15:93,595,338 | C/T | — | uncertain significance |
| rs2505700694 | 15:93,595,353 | C/T | — | uncertain significance |
| rs774790049 | 15:93,595,386 | G/A | — | uncertain significance |
| rs765965633 | 15:93,595,404 | G/A | — | uncertain significance |
| rs762713342 | 15:93,595,485 | G/A | — | uncertain significance |
| rs779250806 | 15:93,595,497 | G/A | — | uncertain significance |
| rs762554909 | 15:93,595,552 | T/C | — | uncertain significance |
| rs374516123 | 15:93,595,561 | C/T | — | uncertain significance |
| rs201701610 | 15:93,595,648 | C/T | — | uncertain significance |
| rs2505702421 | 15:93,595,714 | T/G | — | uncertain significance |
| rs140514824 | 15:93,596,695 | C/G | intron variant | — |
| rs2505749772 | 15:93,616,201 | C/G | — | uncertain significance |
| rs369702106 | 15:93,616,208 | C/T | — | uncertain significance |
| rs767006823 | 15:93,616,213 | C/T | — | uncertain significance |
| rs1895383747 | 15:93,616,220 | T/C | — | uncertain significance |
| rs373577763 | 15:93,616,235 | C/T | — | uncertain significance |
| rs1318044179 | 15:93,616,252 | A/G | — | uncertain significance |
| rs3942115 | 15:93,616,946 | A/G | — | benign |
| rs1306335519 | 15:93,616,955 | T/G | — | uncertain significance |
| rs755463441 | 15:93,616,973 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.