SLC39A11
solute carrier family 39 member 11
Summary
Predicted to enable copper ion transmembrane transporter activity and zinc ion transmembrane transporter activity. Predicted to be involved in zinc ion transmembrane transport. Predicted to be located in Golgi apparatus; nucleus; and plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7210086 | 17:70,641,698 | A/C | downstream gene variant | — |
| rs143270631 | 17:70,643,737 | C/T | — | uncertain significance |
| rs532763313 | 17:70,644,979 | C/T | — | uncertain significance |
| rs374143884 | 17:70,645,352 | G/T | — | uncertain significance |
| rs188609955 | 17:70,655,785 | G/A | downstream gene variant | — |
| rs8066857 | 17:70,696,103 | C/T | regulatory region variant | — |
| rs891684 | 17:70,713,539 | G/C | — | — |
| rs11871756 | 17:70,726,244 | C/G | regulatory region variant | — |
| rs779334624 | 17:70,732,816 | G/A | — | uncertain significance |
| rs2567519 | 17:70,788,406 | G/A | intron variant | — |
| rs12943829 | 17:70,826,404 | G/C | intron variant | — |
| rs745762301 | 17:70,845,779 | C/A | — | uncertain significance |
| rs1351136187 | 17:70,845,782 | T/C | — | uncertain significance |
| rs144832523 | 17:70,845,790 | G/A | — | uncertain significance |
| rs970953677 | 17:70,845,817 | C/T | — | uncertain significance |
| rs1027614641 | 17:70,845,822 | C/G | — | uncertain significance |
| rs373163649 | 17:70,845,832 | C/T | — | uncertain significance |
| rs2511302590 | 17:70,845,877 | G/A | — | uncertain significance |
| rs2511302796 | 17:70,845,881 | C/T | — | uncertain significance |
| rs12051560 | 17:70,898,201 | G/A | intron variant | — |
| rs17183225 | 17:70,912,437 | C/T | intron variant | — |
| rs17780814 | 17:70,912,465 | A/T | — | — |
| rs17780820 | 17:70,912,517 | T/C | intron variant | — |
| rs2509559755 | 17:70,943,885 | C/T | — | uncertain significance |
| rs2085524968 | 17:70,943,915 | C/T | — | uncertain significance |
| rs1384059126 | 17:70,943,932 | G/A | — | uncertain significance |
| rs149939873 | 17:70,943,973 | G/A | — | likely benign |
| rs34970573 | 17:70,944,008 | C/T | — | likely benign |
| rs4969049 | 17:71,000,940 | T/C | intron variant | — |
| rs11077654 | 17:71,006,512 | A/T | — | — |
| rs35780242 | 17:71,007,980 | G/T | intron variant | — |
| rs9913017 | 17:71,011,020 | A/T | — | — |
| rs4969054 | 17:71,012,473 | G/C | intron variant | — |
| rs2510332151 | 17:71,027,700 | G/C | — | uncertain significance |
| rs1221100895 | 17:71,027,712 | G/A | — | uncertain significance |
| rs760246609 | 17:71,027,741 | A/G | — | uncertain significance |
| rs199758218 | 17:71,027,745 | T/C | — | uncertain significance |
| rs372107398 | 17:71,027,764 | G/C | — | uncertain significance |
| rs145755722 | 17:71,027,802 | C/A | — | uncertain significance |
| rs1323832314 | 17:71,027,848 | C/T | — | uncertain significance |
| rs903107 | 17:71,061,934 | T/C | downstream gene variant | — |
| rs8081059 | 17:71,068,719 | C/G | — | — |
| rs8065544 | 17:71,068,942 | G/T | — | — |
| rs760653145 | 17:71,080,972 | T/C | — | uncertain significance |
| rs78761885 | 17:71,080,981 | C/T | — | benign |
| rs138272257 | 17:71,084,798 | G/C | — | uncertain significance |
| rs145169937 | 17:71,084,813 | C/T | — | likely benign |
| rs146208211 | 17:71,084,844 | C/T | — | likely benign |
| rs1447447061 | 17:71,084,860 | G/T | — | uncertain significance |
| rs148439735 | 17:71,084,898 | G/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.