HNF4G
hepatocyte nuclear factor 4 gamma
Summary
Enables DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II. Located in several cellular components, including intercellular bridge; mitotic spindle; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1800921 | 8:76,320,110 | A/G | regulatory region variant | — |
| rs189268208 | 8:76,360,637 | A/G | intron variant | — |
| rs77143074 | 8:76,362,032 | G/T | — | — |
| rs6994463 | 8:76,366,390 | C/T | intron variant | — |
| rs1964528 | 8:76,390,058 | C/T | intron variant | — |
| rs2943559 | 8:76,417,937 | A/G | intron variant | — |
| rs76847940 | 8:76,442,925 | G/T | intron variant | — |
| rs76283120 | 8:76,451,748 | T/C | upstream gene variant | — |
| rs773555360 | 8:76,452,267 | T/G | — | uncertain significance |
| rs753142130 | 8:76,452,292 | T/C | — | uncertain significance |
| rs2977929 | 8:76,454,025 | C/T | intron variant | — |
| rs1231597503 | 8:76,456,208 | C/A | — | uncertain significance |
| rs184639867 | 8:76,458,571 | C/G | intron variant | — |
| rs531645254 | 8:76,459,829 | C/T | — | uncertain significance |
| rs1468793979 | 8:76,463,696 | C/A | — | uncertain significance |
| rs147422598 | 8:76,463,718 | C/T | — | uncertain significance |
| rs541464310 | 8:76,465,316 | G/A | — | uncertain significance |
| rs774229582 | 8:76,465,355 | A/G | — | uncertain significance |
| rs887807990 | 8:76,465,414 | A/C | — | uncertain significance |
| rs750483077 | 8:76,465,418 | C/T | — | uncertain significance |
| rs770191630 | 8:76,468,246 | G/C | — | uncertain significance |
| rs2941471 | 8:76,470,404 | G/A | intron variant | — |
| rs761403019 | 8:76,470,801 | G/A | — | uncertain significance |
| rs749953451 | 8:76,470,810 | A/G | — | uncertain significance |
| rs779068332 | 8:76,471,055 | T/A | — | uncertain significance |
| rs2488102255 | 8:76,471,092 | A/G | — | uncertain significance |
| rs1807217194 | 8:76,471,170 | A/G | — | uncertain significance |
| rs1275830536 | 8:76,471,195 | T/C | — | uncertain significance |
| rs2488103634 | 8:76,471,205 | A/C | — | uncertain significance |
| rs61755717 | 8:76,471,236 | A/G | — | uncertain significance |
| rs373673448 | 8:76,472,588 | A/G | — | uncertain significance |
| rs2488129751 | 8:76,476,243 | A/G | — | uncertain significance |
| rs2941484 | 8:76,478,768 | C/T | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.