TNFAIP6
TNF alpha induced protein 6
Summary
The protein encoded by this gene is a secretory protein that contains a hyaluronan-binding domain, and thus is a member of the hyaluronan-binding protein family. The hyaluronan-binding domain is known to be involved in extracellular matrix stability and cell migration. This protein has been shown to form a stable complex with inter-alpha-inhibitor (I alpha I), and thus enhance the serine protease inhibitory activity of I alpha I, which is important in the protease network associated with inflammation. This gene can be induced by proinflammatory cytokines such as tumor necrosis factor alpha and interleukin-1. Enhanced levels of this protein are found in the synovial fluid of patients with osteoarthritis and rheumatoid arthritis.[provided by RefSeq, Dec 2010]
Known Variants17 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10930576 | 2:152,212,156 | C/A | upstream gene variant | — |
| rs766282193 | 2:152,214,211 | C/G | — | uncertain significance |
| rs761269991 | 2:152,220,460 | G/T | — | uncertain significance |
| rs1308388959 | 2:152,220,486 | G/C | — | uncertain significance |
| rs566948911 | 2:152,220,490 | G/T | — | uncertain significance |
| rs375585000 | 2:152,220,506 | G/T | — | uncertain significance |
| rs138376471 | 2:152,220,555 | C/G | — | uncertain significance |
| rs774746563 | 2:152,222,606 | G/A | — | uncertain significance |
| rs77964389 | 2:152,225,719 | C/A | upstream gene variant | — |
| rs144393744 | 2:152,226,541 | G/C | — | uncertain significance |
| rs564029423 | 2:152,226,551 | G/A | — | uncertain significance |
| rs1684789547 | 2:152,226,644 | T/C | — | uncertain significance |
| rs780367746 | 2:152,226,654 | G/A | — | likely benign |
| rs771155983 | 2:152,230,073 | G/A | — | uncertain significance |
| rs774196085 | 2:152,235,952 | A/G | — | likely benign |
| rs757631554 | 2:152,235,991 | A/T | — | uncertain significance |
| rs183754548 | 2:152,238,019 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.