| Entrez Gene ID | 100505738 |
|---|---|
| Official Gene Symbol | MIR4458HG (GeneCards) |
| Full name | MIR4458 host gene |
| Location | 5p15.31 |
| Other ids | HGNC : HGNC:49008 Ensembl : ENSG00000247516 |
| Other names | None |
| Summary | None |
Found 6 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 7481 | 100505738 | MIR4458HG | 5 | 8767405 | 8767405 | Asymptomatic | HiSeq X Ten |
| 7495 | 100505738 | MIR4458HG | 5 | 8831632 | 8831632 | Asymptomatic | HiSeq X Ten |
| 7824 | 100505738 | MIR4458HG | 5 | 8828937 | 8828937 | Asymptomatic | HiSeq X Ten |
| 7911 | 100505738 | MIR4458HG | 5 | 8778121 | 8778121 | Asymptomatic | HiSeq X Ten |
| 8647 | 100505738 | MIR4458HG | 5 | 8705707 | 8705707 | Cockayne syndrome | HiSeq X Ten |
| 8685 | 100505738 | MIR4458HG | 5 | 8628653 | 8628653 | Cockayne syndrome | HiSeq X Ten |