TNIP2
TNFAIP3 interacting protein 2
Summary
This gene encodes a protein which acts as an inhibitor of NFkappaB activation. The encoded protein is also involved in MAP/ERK signaling pathway in specific cell types. It may be involved in apoptosis of endothelial cells. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the X chromosome.[provided by RefSeq, May 2014]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs112837508 | 4:2,744,091 | C/T | — | likely benign |
| rs1721815143 | 4:2,744,093 | C/T | — | uncertain significance |
| rs148479255 | 4:2,744,132 | G/A | — | uncertain significance |
| rs145021348 | 4:2,744,229 | C/G | — | uncertain significance |
| rs144921267 | 4:2,744,240 | C/T | — | likely benign |
| rs3733223 | 4:2,745,508 | C/A | intron variant | — |
| rs754131078 | 4:2,746,134 | G/A | — | uncertain significance |
| rs143796684 | 4:2,746,146 | C/T | — | likely benign |
| rs1577306836 | 4:2,746,448 | C/G | — | uncertain significance |
| rs1302602592 | 4:2,746,458 | G/A | — | uncertain significance |
| rs745310133 | 4:2,746,465 | G/A | — | uncertain significance |
| rs2530159893 | 4:2,746,613 | C/G | — | uncertain significance |
| rs1228360081 | 4:2,746,614 | C/G | — | uncertain significance |
| rs768831983 | 4:2,746,618 | C/A | — | uncertain significance |
| rs770013204 | 4:2,746,624 | C/T | — | uncertain significance |
| rs147415827 | 4:2,746,645 | G/A | — | uncertain significance |
| rs766985672 | 4:2,746,646 | C/A | — | uncertain significance |
| rs2530160063 | 4:2,746,663 | G/A | — | uncertain significance |
| rs751887872 | 4:2,747,180 | A/G | — | uncertain significance |
| rs150960773 | 4:2,747,198 | C/T | — | uncertain significance |
| rs1010415009 | 4:2,747,216 | T/C | — | uncertain significance |
| rs760797347 | 4:2,749,399 | C/G | — | uncertain significance |
| rs141461185 | 4:2,749,486 | G/A | — | uncertain significance |
| rs551215045 | 4:2,749,508 | C/G | — | uncertain significance |
| rs145102753 | 4:2,749,516 | G/A | — | uncertain significance |
| rs138986059 | 4:2,749,525 | C/T | — | likely benign |
| rs1193246266 | 4:2,749,528 | C/T | — | uncertain significance |
| rs762906038 | 4:2,749,593 | C/T | — | uncertain significance |
| rs2530167249 | 4:2,749,602 | T/G | — | uncertain significance |
| rs199596183 | 4:2,749,614 | A/C | — | uncertain significance |
| rs10937913 | 4:2,752,425 | A/G | intron variant | — |
| rs2530184575 | 4:2,757,793 | C/T | — | uncertain significance |
| rs2530184633 | 4:2,757,802 | G/A | — | uncertain significance |
| rs775612361 | 4:2,757,827 | C/T | — | uncertain significance |
| rs1164339656 | 4:2,757,868 | G/T | — | uncertain significance |
| rs762485876 | 4:2,757,909 | G/C | — | uncertain significance |
| rs1207593036 | 4:2,757,981 | C/G | — | uncertain significance |
| rs779245238 | 4:2,758,009 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.