PHF24
PHD finger protein 24
Summary
Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to act upstream of or within several processes, including detection of mechanical stimulus involved in sensory perception of pain; gamma-aminobutyric acid signaling pathway; and regulation of GABAergic synaptic transmission. Predicted to be active in glutamatergic synapse; nucleus; and synaptic vesicle membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs28409914 | 9:34,720,464 | C/A | downstream gene variant | — |
| rs2492358 | 9:34,737,828 | C/T | intergenic variant | — |
| rs951005 | 9:34,743,681 | G/T | — | — |
| rs13293020 | 9:34,768,693 | C/G | — | — |
| rs10758278 | 9:34,825,303 | G/A | intergenic variant | — |
| rs12339911 | 9:34,845,984 | T/G | — | — |
| rs115567907 | 9:34,893,047 | C/G | coding sequence variant | — |
| rs560059370 | 9:34,931,100 | C/G | — | — |
| rs772330236 | 9:34,971,317 | C/T | — | uncertain significance |
| rs763902553 | 9:34,971,372 | A/T | — | uncertain significance |
| rs894237442 | 9:34,971,399 | G/A | — | uncertain significance |
| rs377061980 | 9:34,971,425 | C/T | — | uncertain significance |
| rs201890559 | 9:34,971,428 | C/T | — | uncertain significance |
| rs775490664 | 9:34,971,429 | G/A | — | uncertain significance |
| rs1158745245 | 9:34,971,432 | G/T | — | uncertain significance |
| rs996494462 | 9:34,971,518 | G/A | — | uncertain significance |
| rs763005447 | 9:34,971,521 | C/T | — | uncertain significance |
| rs374394658 | 9:34,971,537 | G/A | — | uncertain significance |
| rs1204858419 | 9:34,971,578 | A/G | — | uncertain significance |
| rs372641183 | 9:34,971,621 | G/A | — | uncertain significance |
| rs1340457594 | 9:34,971,654 | G/T | — | uncertain significance |
| rs1827023365 | 9:34,972,364 | G/A | — | uncertain significance |
| rs754208132 | 9:34,972,446 | G/A | — | uncertain significance |
| rs1025167852 | 9:34,972,476 | C/T | — | uncertain significance |
| rs774639353 | 9:34,976,568 | G/A | — | uncertain significance |
| rs373860524 | 9:34,976,730 | G/A | — | uncertain significance |
| rs2490150066 | 9:34,977,083 | T/C | — | uncertain significance |
| rs536419897 | 9:34,977,131 | G/A | — | likely benign |
| rs367738071 | 9:34,977,132 | C/T | — | uncertain significance |
| rs771816039 | 9:34,977,143 | C/T | — | uncertain significance |
| rs375687553 | 9:34,977,179 | C/T | — | uncertain significance |
| rs573160141 | 9:34,977,207 | A/G | — | uncertain significance |
| rs377513712 | 9:34,977,600 | T/G | — | uncertain significance |
| rs2490165397 | 9:34,978,071 | C/G | — | uncertain significance |
| rs2490165573 | 9:34,978,080 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.