AMIGO1
adhesion molecule with Ig like domain 1
Summary
Predicted to enable potassium channel regulator activity. Predicted to be involved in several processes, including heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules; nervous system development; and positive regulation of nervous system development. Predicted to be located in dendrite; neuronal cell body membrane; and voltage-gated potassium channel complex. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants22 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs14184 | 1:110,047,110 | C/G | downstream gene variant | — |
| rs1005277760 | 1:110,050,111 | C/T | — | uncertain significance |
| rs139892756 | 1:110,050,153 | T/A | — | uncertain significance |
| rs150743133 | 1:110,050,180 | C/T | missense variant | — |
| rs759291273 | 1:110,050,216 | C/T | — | uncertain significance |
| rs776166736 | 1:110,050,271 | T/A | — | uncertain significance |
| rs2524163904 | 1:110,050,303 | C/G | — | uncertain significance |
| rs914949225 | 1:110,050,325 | C/T | — | uncertain significance |
| rs149188606 | 1:110,050,330 | C/T | — | uncertain significance |
| rs1399747783 | 1:110,050,340 | A/G | — | uncertain significance |
| rs1432138584 | 1:110,050,394 | T/C | — | uncertain significance |
| rs2101060005 | 1:110,050,399 | C/T | — | uncertain significance |
| rs906853923 | 1:110,050,614 | T/G | — | uncertain significance |
| rs779480021 | 1:110,050,628 | T/C | — | uncertain significance |
| rs765333109 | 1:110,050,708 | C/T | — | uncertain significance |
| rs2524165113 | 1:110,050,765 | T/C | — | uncertain significance |
| rs1658077731 | 1:110,050,927 | G/A | — | uncertain significance |
| rs2524165506 | 1:110,050,985 | G/C | — | uncertain significance |
| rs376002984 | 1:110,051,212 | G/A | — | uncertain significance |
| rs780446508 | 1:110,051,287 | G/C | — | uncertain significance |
| rs375349763 | 1:110,051,453 | C/T | — | uncertain significance |
| rs146766120 | 1:110,051,462 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.