MS4A14
membrane spanning 4-domains A14
Summary
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs367787186 | 11:60,167,880 | A/G | — | uncertain significance |
| rs77796224 | 11:60,167,897 | C/G | — | benign |
| rs771943812 | 11:60,170,481 | T/A | — | uncertain significance |
| rs567429522 | 11:60,170,494 | C/T | — | uncertain significance |
| rs117531239 | 11:60,178,306 | T/G | — | — |
| rs550060785 | 11:60,182,929 | C/T | — | uncertain significance |
| rs148391374 | 11:60,182,971 | A/G | — | uncertain significance |
| rs2135154399 | 11:60,182,985 | T/A | — | uncertain significance |
| rs757889474 | 11:60,183,016 | A/T | — | uncertain significance |
| rs369024994 | 11:60,183,018 | T/C | — | uncertain significance |
| rs142563385 | 11:60,183,024 | A/G | — | uncertain significance |
| rs759771229 | 11:60,183,039 | G/C | — | uncertain significance |
| rs1042810200 | 11:60,183,063 | T/C | — | uncertain significance |
| rs370208539 | 11:60,183,091 | T/C | — | uncertain significance |
| rs2495300052 | 11:60,183,097 | C/T | — | likely benign |
| rs1339543249 | 11:60,183,267 | G/C | — | uncertain significance |
| rs768895069 | 11:60,183,279 | C/A | — | uncertain significance |
| rs2495301483 | 11:60,183,282 | T/A | — | uncertain significance |
| rs114064661 | 11:60,183,297 | C/A | — | uncertain significance |
| rs2495301865 | 11:60,183,325 | A/G | — | uncertain significance |
| rs762771758 | 11:60,183,378 | G/A | — | uncertain significance |
| rs145539034 | 11:60,183,517 | G/A | — | likely benign |
| rs1018732573 | 11:60,183,553 | T/C | — | uncertain significance |
| rs761288448 | 11:60,183,595 | T/A | — | uncertain significance |
| rs768485346 | 11:60,183,676 | C/T | — | uncertain significance |
| rs747809669 | 11:60,183,684 | A/G | — | uncertain significance |
| rs3802959 | 11:60,183,793 | A/G | — | uncertain significance |
| rs1412279172 | 11:60,183,806 | G/A | — | uncertain significance |
| rs139435636 | 11:60,183,835 | T/G | — | uncertain significance |
| rs376488191 | 11:60,183,894 | C/T | — | uncertain significance |
| rs756018369 | 11:60,184,058 | C/G | — | uncertain significance |
| rs1446895769 | 11:60,184,216 | A/G | — | uncertain significance |
| rs1401658674 | 11:60,184,412 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.