FOXJ2
forkhead box J2
Summary
Enables DNA-binding transcription activator activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and identical protein binding activity. Involved in several processes, including negative regulation of angiogenesis; negative regulation of blood vessel endothelial cell differentiation; and positive regulation of vascular associated smooth muscle cell proliferation. Located in fibrillar center and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs745455298 | 12:8,192,609 | G/T | — | uncertain significance |
| rs369499195 | 12:8,192,613 | A/G | — | uncertain significance |
| rs925597042 | 12:8,192,631 | G/A | — | uncertain significance |
| rs55680021 | 12:8,195,577 | C/T | intron variant | — |
| rs781177580 | 12:8,196,309 | A/T | — | uncertain significance |
| rs141186868 | 12:8,196,312 | A/G | — | uncertain significance |
| rs763636480 | 12:8,196,354 | C/T | — | uncertain significance |
| rs929824936 | 12:8,196,572 | A/T | — | uncertain significance |
| rs148391914 | 12:8,196,598 | G/A | — | uncertain significance |
| rs1426031890 | 12:8,196,641 | C/T | — | uncertain significance |
| rs2498050867 | 12:8,197,395 | G/C | — | uncertain significance |
| rs761035927 | 12:8,197,454 | T/A | — | uncertain significance |
| rs750445406 | 12:8,197,483 | A/G | — | uncertain significance |
| rs200052277 | 12:8,197,525 | T/G | — | uncertain significance |
| rs140318415 | 12:8,197,546 | C/G | — | uncertain significance |
| rs1345668109 | 12:8,200,518 | C/G | — | uncertain significance |
| rs541007096 | 12:8,200,580 | C/T | — | uncertain significance |
| rs201863216 | 12:8,200,721 | C/T | — | uncertain significance |
| rs1442392090 | 12:8,200,777 | G/A | — | uncertain significance |
| rs1179227695 | 12:8,200,799 | A/G | — | uncertain significance |
| rs145233499 | 12:8,200,880 | G/C | — | uncertain significance |
| rs1369997360 | 12:8,201,305 | A/G | — | uncertain significance |
| rs749168304 | 12:8,201,380 | A/G | — | uncertain significance |
| rs763564059 | 12:8,201,976 | G/A | — | uncertain significance |
| rs760030335 | 12:8,202,110 | C/T | — | uncertain significance |
| rs143592450 | 12:8,202,111 | G/A | — | uncertain significance |
| rs1328340057 | 12:8,203,135 | C/T | — | uncertain significance |
| rs722458 | 12:8,204,575 | G/A | intron variant | — |
| rs376963092 | 12:8,205,403 | A/G | — | likely benign |
| rs932463156 | 12:8,205,404 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.