MACO1
macoilin 1
Summary
Predicted to enable microtubule binding activity. Involved in neuronal signal transduction. Located in rough endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1422681732 | 1:25,757,629 | C/A | — | uncertain significance |
| rs2042861391 | 1:25,757,665 | G/T | — | uncertain significance |
| rs9438905 | 1:25,764,177 | A/T | — | — |
| rs9438909 | 1:25,766,465 | T/C | intron variant | — |
| rs10903129 | 1:25,768,937 | A/G | regulatory region variant | — |
| rs78464742 | 1:25,775,326 | G/A | — | uncertain significance |
| rs12027110 | 1:25,775,682 | A/T | intron variant | — |
| rs12027135 | 1:25,775,733 | A/T | intron variant | — |
| rs7554255 | 1:25,778,106 | C/T | intron variant | — |
| rs4649085 | 1:25,778,832 | G/A | intron variant | — |
| rs7519530 | 1:25,779,236 | T/A | — | — |
| rs113398522 | 1:25,780,773 | G/A | — | uncertain significance |
| rs536920971 | 1:25,783,190 | G/T | — | uncertain significance |
| rs2523629179 | 1:25,783,298 | A/C | — | uncertain significance |
| rs202095871 | 1:25,783,303 | A/C | — | uncertain significance |
| rs182729817 | 1:25,784,896 | C/T | — | uncertain significance |
| rs1334174959 | 1:25,785,104 | A/G | — | uncertain significance |
| rs145917972 | 1:25,785,206 | G/C | — | uncertain significance |
| rs2523636874 | 1:25,785,218 | A/G | — | uncertain significance |
| rs760217519 | 1:25,785,271 | A/G | — | uncertain significance |
| rs2523637556 | 1:25,785,382 | A/G | — | uncertain significance |
| rs35189848 | 1:25,788,422 | A/G | regulatory region variant | — |
| rs192747354 | 1:25,790,409 | G/A | intron variant | — |
| rs34054126 | 1:25,792,915 | G/T | — | — |
| rs570398878 | 1:25,798,891 | T/C | — | — |
| rs35065124 | 1:25,806,112 | T/G | — | — |
| rs61775192 | 1:25,810,416 | A/C | — | — |
| rs767856216 | 1:25,810,738 | G/A | — | uncertain significance |
| rs115063739 | 1:25,811,926 | T/C | intron variant | — |
| rs2043423096 | 1:25,812,137 | C/G | — | uncertain significance |
| rs35225089 | 1:25,813,620 | T/C | intron variant | — |
| rs35945278 | 1:25,813,811 | C/A | intron variant | — |
| rs545022449 | 1:25,815,725 | C/T | — | uncertain significance |
| rs774459628 | 1:25,815,729 | C/A | — | uncertain significance |
| rs766707174 | 1:25,815,772 | A/C | — | uncertain significance |
| rs115337209 | 1:25,817,704 | T/C | intron variant | — |
| rs115340137 | 1:25,818,182 | T/C | intron variant | — |
| rs34791230 | 1:25,818,398 | G/T | — | — |
| rs72660961 | 1:25,818,452 | C/T | intron variant | — |
| rs764516333 | 1:25,824,934 | G/A | — | uncertain significance |
| rs67125653 | 1:25,825,950 | G/C | — | — |
| rs72660967 | 1:25,825,956 | T/A | — | — |
| rs145389033 | 1:25,826,096 | A/G | 3 prime UTR variant | — |
| rs34491689 | 1:25,826,502 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.