FAM89B
family with sequence similarity 89 member B
Summary
Predicted to enable transcription corepressor binding activity. Predicted to be involved in establishment of cell polarity; negative regulation of transmembrane receptor protein serine/threonine kinase signaling pathway; and positive regulation of cell migration. Predicted to be located in cell projection. Predicted to be active in cytoplasm and lamellipodium. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants12 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10896017 | 11:65,340,135 | C/T | regulatory region variant | — |
| rs949597634 | 11:65,340,147 | G/A | — | uncertain significance |
| rs1857155029 | 11:65,340,243 | G/T | — | uncertain significance |
| rs987797650 | 11:65,340,345 | G/T | — | uncertain significance |
| rs1249208835 | 11:65,340,352 | C/T | — | uncertain significance |
| rs905404078 | 11:65,340,373 | C/T | — | uncertain significance |
| rs1857159080 | 11:65,340,387 | C/T | — | uncertain significance |
| rs2496217756 | 11:65,340,933 | T/C | — | uncertain significance |
| rs374813667 | 11:65,340,950 | C/T | — | likely benign |
| rs1047423258 | 11:65,340,986 | G/A | — | likely benign |
| rs1488620917 | 11:65,341,014 | G/A | — | uncertain significance |
| rs753891511 | 11:65,341,075 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.