ARID3B
AT-rich interaction domain 3B
Summary
This gene encodes a member of the ARID (AT-rich interaction domain) family of DNA-binding proteins. The encoded protein is homologous with two proteins that bind to the retinoblastoma gene product, and also with the mouse Bright and Drosophila dead ringer proteins. A pseudogene on chromosome 1p31 exists for this gene. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs751127718 | 15:74,836,290 | C/G | — | uncertain significance |
| rs2061605152 | 15:74,836,438 | C/T | — | uncertain significance |
| rs975080800 | 15:74,836,665 | C/G | — | uncertain significance |
| rs779215718 | 15:74,836,716 | C/T | — | uncertain significance |
| rs374850745 | 15:74,836,752 | A/G | — | uncertain significance |
| rs2061607777 | 15:74,836,767 | G/A | — | uncertain significance |
| rs761652462 | 15:74,836,774 | C/T | — | uncertain significance |
| rs117419740 | 15:74,837,907 | G/A | intron variant | — |
| rs748920116 | 15:74,865,218 | T/C | — | uncertain significance |
| rs2505127831 | 15:74,865,272 | A/G | — | uncertain significance |
| rs139222319 | 15:74,865,527 | G/A | — | likely benign |
| rs188468626 | 15:74,880,600 | A/G | intron variant | — |
| rs148447597 | 15:74,882,175 | C/A | — | benign |
| rs141741770 | 15:74,882,252 | G/A | — | benign |
| rs772776093 | 15:74,883,592 | C/T | — | uncertain significance |
| rs994507193 | 15:74,883,658 | G/A | — | uncertain significance |
| rs769141557 | 15:74,883,659 | G/C | — | uncertain significance |
| rs1436826768 | 15:74,883,939 | C/T | — | uncertain significance |
| rs372219475 | 15:74,883,984 | C/G | — | uncertain significance |
| rs113614863 | 15:74,884,074 | C/T | — | uncertain significance |
| rs561048524 | 15:74,884,120 | G/A | — | uncertain significance |
| rs1206939308 | 15:74,884,149 | G/A | — | uncertain significance |
| rs756104705 | 15:74,885,530 | T/G | — | uncertain significance |
| rs147808851 | 15:74,887,959 | G/A | — | benign |
| rs750249678 | 15:74,888,026 | A/G | — | uncertain significance |
| rs2505160923 | 15:74,888,083 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.