MOBP
myelin associated oligodendrocyte basic protein
Summary
Predicted to be a structural constituent of myelin sheath. Predicted to be involved in nervous system development. Predicted to be located in mitochondrion and perinuclear region of cytoplasm. Implicated in frontotemporal dementia. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants18 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs35650892 | 3:39,510,285 | G/T | — | — |
| rs13067055 | 3:39,510,517 | A/G | intron variant | — |
| rs28810495 | 3:39,510,655 | G/A | intron variant | — |
| rs538867 | 3:39,513,278 | C/T | intron variant | — |
| rs1768208 | 3:39,523,003 | T/C | intron variant | — |
| rs562545 | 3:39,536,524 | A/T | — | — |
| rs9854526 | 3:39,540,914 | C/A | — | — |
| rs200848695 | 3:39,543,626 | C/A | — | uncertain significance |
| rs764606840 | 3:39,543,652 | C/T | — | uncertain significance |
| rs768845645 | 3:39,543,771 | G/C | — | uncertain significance |
| rs185064368 | 3:39,543,999 | G/A | — | likely benign |
| rs755066817 | 3:39,544,069 | C/T | — | uncertain significance |
| rs781467178 | 3:39,544,079 | C/T | — | uncertain significance |
| rs995835006 | 3:39,544,180 | C/T | — | likely benign |
| rs1188260744 | 3:39,544,333 | C/A | — | uncertain significance |
| rs816488 | 3:39,553,788 | C/T | intron variant | — |
| rs2233204 | 3:39,554,786 | C/T | intron variant | — |
| rs864643 | 3:39,555,580 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.