MLXIP
MLX interacting protein
Summary
This gene encodes a protein that functions as part of a heterodimer to activate transcription. The encoded protein forms a heterodimer with Max-like protein X (MLX) and is involved in the regulation of genes in response to cellular glucose levels. [provided by RefSeq, Mar 2014]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2546982588 | 12:122,516,865 | G/T | — | uncertain significance |
| rs1952051823 | 12:122,516,893 | G/A | — | uncertain significance |
| rs749022808 | 12:122,516,895 | G/A | — | uncertain significance |
| rs2546982929 | 12:122,516,937 | C/T | — | uncertain significance |
| rs2546983091 | 12:122,516,995 | G/A | — | uncertain significance |
| rs61952922 | 12:122,520,575 | A/G | regulatory region variant | — |
| rs139779037 | 12:122,522,165 | C/T | regulatory region variant | — |
| rs146154021 | 12:122,522,921 | T/C | intron variant | — |
| rs36163299 | 12:122,528,275 | T/C | intron variant | — |
| rs144305620 | 12:122,583,527 | G/A | intron variant | — |
| rs36168754 | 12:122,589,825 | G/T | — | — |
| rs28731286 | 12:122,591,751 | T/G | — | — |
| rs56072019 | 12:122,595,618 | T/G | — | — |
| rs28421373 | 12:122,598,594 | A/G | regulatory region variant | — |
| rs28498002 | 12:122,599,796 | C/G | — | — |
| rs28707337 | 12:122,600,134 | T/G | — | — |
| rs28430881 | 12:122,602,899 | C/G | — | — |
| rs4132933 | 12:122,605,949 | G/A | intron variant | — |
| rs4132934 | 12:122,606,176 | A/G | intron variant | — |
| rs114855183 | 12:122,606,596 | A/T | — | — |
| rs4758690 | 12:122,610,909 | G/A | intron variant | — |
| rs2547040729 | 12:122,612,430 | A/G | — | uncertain significance |
| rs2547044455 | 12:122,614,156 | G/C | — | uncertain significance |
| rs2547046155 | 12:122,614,608 | T/C | — | uncertain significance |
| rs11061153 | 12:122,615,033 | G/C | — | — |
| rs11061602 | 12:122,615,964 | G/C | — | — |
| rs11061610 | 12:122,616,240 | T/C | intron variant | — |
| rs2547052074 | 12:122,618,117 | C/T | — | uncertain significance |
| rs369537342 | 12:122,618,264 | G/A | — | uncertain significance |
| rs2547052785 | 12:122,618,384 | G/A | — | uncertain significance |
| rs2547053211 | 12:122,618,516 | A/G | — | uncertain significance |
| rs1414966423 | 12:122,620,039 | C/T | — | uncertain significance |
| rs2547056070 | 12:122,620,133 | G/A | — | uncertain significance |
| rs2547061048 | 12:122,622,817 | G/A | — | uncertain significance |
| rs7953704 | 12:122,625,992 | A/G | intron variant | — |
| rs11057509 | 12:122,626,381 | G/T | — | — |
| rs4758685 | 12:122,626,842 | G/A | 3 prime UTR variant | — |
| rs3741452 | 12:122,628,429 | T/C | — | — |
| rs1043763 | 12:122,630,909 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.