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Gene Information
Gene symbol: PHF10
Gene name: PHD finger protein 10
HGNC ID: 18250
Synonyms: FLJ10975, XAP135
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | C6orf120 | 1 hits |
| 2 | C6orf208 | 1 hits |
| 3 | C6orf70 | 1 hits |
| 4 | CCR6 | 1 hits |
| 5 | DLL1 | 1 hits |
| 6 | FAM120B | 1 hits |
| 7 | PDCD2 | 1 hits |
| 8 | PSMB1 | 1 hits |
| 9 | TBP | 1 hits |
| 10 | TCTE3 | 1 hits |
| 11 | WDR27 | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 15850778 | Using a much larger sample of T1D families than those studied by others, and by extensive re-sequencing of nine other genes in the proximity, in which we identified 279 polymorphisms, 83 of which were genotyped in up to 725 T1D multiplex and simplex families, we obtained no evidence for association of the TBP CAG/CAA (glutamine) microsatellite repeat sequence with disease, or for nine other genes, PDCD2, PSMB1, KIAA1838, DLL1, dJ894D12.4, FLJ25454, FLJ13162, FLJ11152, PHF10 and CCR6. |
| 2 | 21980299 | The most significantly associated SNP (rs539514, P = 5.66×10⁻¹¹) resides in an intronic region of the LMO7 (LIM domain only 7) gene on 13q22. |
| 3 | 21980299 | The second most significantly associated SNP (rs478222, P = 3.50×10⁻⁹ resides in an intronic region of the EFR3B (protein EFR3 homolog B) gene on 2p23; however, the region of linkage disequilibrium is approximately 800 kb and harbors additional multiple genes, including NCOA1, C2orf79, CENPO, ADCY3, DNAJC27, POMC, and DNMT3A. |
| 4 | 21980299 | The third most significantly associated SNP (rs924043, P = 8.06×10⁻⁹ lies in an intergenic region on 6q27, where the region of association is approximately 900 kb and harbors multiple genes including WDR27, C6orf120, PHF10, TCTE3, C6orf208, LOC154449, DLL1, FAM120B, PSMB1, TBP, and PCD2. |