TNFRSF19
TNF receptor superfamily member 19
Summary
The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is highly expressed during embryonic development. It has been shown to interact with TRAF family members, and to activate JNK signaling pathway when overexpressed in cells. This receptor is capable of inducing apoptosis by a caspase-independent mechanism, and it is thought to play an essential role in embryonic development. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3814787 | 13:24,152,370 | G/C | upstream gene variant | — |
| rs9553003 | 13:24,152,789 | G/A | regulatory region variant | — |
| rs11841272 | 13:24,153,453 | T/G | regulatory region variant | — |
| rs9553006 | 13:24,158,672 | A/C | intron variant | — |
| rs370996963 | 13:24,164,357 | C/T | — | uncertain significance |
| rs12583417 | 13:24,167,480 | T/C | — | benign |
| rs1212902080 | 13:24,167,523 | C/A | — | uncertain significance |
| rs200993556 | 13:24,167,539 | G/A | missense variant | Uncertain significance |
| rs4770465 | 13:24,168,742 | A/G | intron variant | — |
| rs760538394 | 13:24,190,052 | G/A | — | uncertain significance |
| rs147369656 | 13:24,190,059 | C/G | — | uncertain significance |
| rs1017456976 | 13:24,200,857 | A/C | — | uncertain significance |
| rs368876279 | 13:24,200,926 | C/T | — | uncertain significance |
| rs9510787 | 13:24,205,195 | A/T | — | — |
| rs554763955 | 13:24,233,249 | C/T | — | uncertain significance |
| rs772823173 | 13:24,233,264 | T/C | — | uncertain significance |
| rs777558903 | 13:24,234,533 | A/G | — | uncertain significance |
| rs750011237 | 13:24,234,609 | G/A | — | uncertain significance |
| rs1884292905 | 13:24,234,617 | G/T | — | uncertain significance |
| rs138676880 | 13:24,234,628 | C/T | — | likely benign |
| rs1575667 | 13:24,239,825 | A/G | — | — |
| rs373980471 | 13:24,242,119 | G/A | — | uncertain significance |
| rs747536955 | 13:24,242,158 | C/A | — | uncertain significance |
| rs775794894 | 13:24,242,167 | C/T | — | uncertain significance |
| rs1210242995 | 13:24,242,191 | G/A | — | uncertain significance |
| rs141678624 | 13:24,242,846 | C/T | — | likely benign |
| rs748316827 | 13:24,242,847 | G/A | — | uncertain significance |
| rs1271329032 | 13:24,242,850 | G/A | — | uncertain significance |
| rs758527814 | 13:24,242,968 | A/C | — | uncertain significance |
| rs367870672 | 13:24,242,997 | T/C | — | uncertain significance |
| rs2547614754 | 13:24,243,040 | A/T | — | uncertain significance |
| rs765835816 | 13:24,243,162 | G/A | — | likely benign |
| rs145685720 | 13:24,243,247 | G/A | — | likely benign |
| rs1951708637 | 13:24,243,253 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.