| Entrez Gene ID | 57495 |
|---|---|
| Official Gene Symbol | NWD2 (GeneCards) |
| Full name | NACHT and WD repeat domain containing 2 |
| Location | 4p14 |
| Other ids | Vega : OTTHUMG00000157134 HGNC : HGNC:29229 Ensembl : ENSG00000174145 |
| Other names | KIAA1239 |
| Summary | None |
Found 8 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 6294 | 57495 | NWD2 | 4 | 37312778 | 37312778 | Asymptomatic | HiSeq X Ten |
| 6327 | 57495 | NWD2 | 4 | 37348500 | 37348500 | Asymptomatic | HiSeq X Ten |
| 6366 | 57495 | NWD2 | 4 | 37431722 | 37431722 | Asymptomatic | HiSeq X Ten |
| 6700 | 57495 | NWD2 | 4 | 37353198 | 37353198 | Asymptomatic | HiSeq X Ten |
| 7131 | 57495 | NWD2 | 4 | 37318665 | 37318665 | Cockayne syndrome | HiSeq X Ten |
| 7151 | 57495 | NWD2 | 4 | 37377441 | 37377441 | Cockayne syndrome | HiSeq X Ten |
| 22902 | 57495 | NWD2 | 4 | 37345176 | 37345176 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |
| 29758 | 57495 | NWD2 | 4 | 37446620 | 37446620 | Autism Spectrum Disorders | HiSeq X Ten Single cell Sequencing Cell cloning NextSeq500 |