ASB11
ankyrin repeat and SOCS box containing 11
Summary
The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs751292804 | X:15,301,634 | T/C | — | uncertain significance |
| rs145832401 | X:15,301,713 | G/A | — | uncertain significance |
| rs773872197 | X:15,301,725 | G/A | — | uncertain significance |
| rs772919113 | X:15,301,728 | A/G | — | uncertain significance |
| rs373647947 | X:15,305,997 | G/T | — | likely benign |
| rs773871027 | X:15,306,009 | G/A | — | uncertain significance |
| rs760467867 | X:15,306,030 | C/T | — | uncertain significance |
| rs1191192661 | X:15,306,047 | G/A | — | uncertain significance |
| rs781564627 | X:15,306,083 | C/T | — | uncertain significance |
| rs34025595 | X:15,306,105 | C/T | — | benign |
| rs2519286357 | X:15,306,162 | T/A | — | uncertain significance |
| rs947862737 | X:15,306,166 | C/T | — | likely benign |
| rs143492892 | X:15,307,659 | T/A | — | benign |
| rs368512399 | X:15,307,692 | C/T | — | uncertain significance |
| rs188779336 | X:15,308,292 | C/G | intron variant | — |
| rs144572145 | X:15,311,318 | G/A | — | likely benign |
| rs376376953 | X:15,311,352 | C/T | — | uncertain significance |
| rs773636633 | X:15,311,433 | C/T | — | uncertain significance |
| rs1282369599 | X:15,315,724 | G/C | — | uncertain significance |
| rs1920980264 | X:15,315,759 | G/C | — | uncertain significance |
| rs781653107 | X:15,333,607 | C/T | — | uncertain significance |
| rs763148786 | X:15,333,612 | T/C | — | uncertain significance |
| rs760587692 | X:15,333,669 | G/A | — | uncertain significance |
| rs375899924 | X:15,333,686 | A/C | — | uncertain significance |
| rs1921588379 | X:15,333,688 | A/G | — | uncertain significance |
| rs138718927 | X:15,333,714 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.