ANKRD13B
ankyrin repeat domain 13B
Summary
Enables ubiquitin-modified protein reader activity. Involved in negative regulation of receptor internalization. Located in endosome; perinuclear region of cytoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1022903413 | 17:27,920,644 | T/A | — | uncertain significance |
| rs768824029 | 17:27,920,676 | G/C | — | uncertain significance |
| rs748170622 | 17:27,920,679 | G/T | — | uncertain significance |
| rs766816883 | 17:27,920,715 | C/T | — | uncertain significance |
| rs9901272 | 17:27,932,453 | T/C | — | — |
| rs775947551 | 17:27,934,839 | G/A | — | uncertain significance |
| rs752789986 | 17:27,934,881 | G/A | — | uncertain significance |
| rs199997513 | 17:27,935,094 | C/T | — | uncertain significance |
| rs373543908 | 17:27,935,105 | G/A | — | uncertain significance |
| rs2508663725 | 17:27,936,196 | C/G | — | uncertain significance |
| rs780411568 | 17:27,936,205 | G/A | — | uncertain significance |
| rs755943053 | 17:27,936,268 | G/C | — | uncertain significance |
| rs756604431 | 17:27,937,761 | A/G | — | uncertain significance |
| rs771066018 | 17:27,938,964 | A/G | — | uncertain significance |
| rs2034603283 | 17:27,939,258 | C/G | — | uncertain significance |
| rs145870428 | 17:27,939,436 | C/T | — | likely benign |
| rs867319835 | 17:27,939,539 | G/A | — | uncertain significance |
| rs571932725 | 17:27,939,681 | G/A | — | uncertain significance |
| rs1244267144 | 17:27,939,688 | A/G | — | uncertain significance |
| rs2508688082 | 17:27,939,726 | A/T | — | uncertain significance |
| rs1409649392 | 17:27,940,404 | C/G | — | uncertain significance |
| rs766734204 | 17:27,940,491 | G/A | — | uncertain significance |
| rs2508697289 | 17:27,940,499 | A/G | — | uncertain significance |
| rs371389990 | 17:27,940,515 | A/T | — | uncertain significance |
| rs1236284432 | 17:27,940,535 | C/T | — | uncertain significance |
| rs1460006789 | 17:27,940,536 | G/A | — | uncertain significance |
| rs1007427181 | 17:27,940,578 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.