| HUGO ID | 1260 |
|---|---|
| Symbol | C21orf2 |
| Name | chromosome 21 open reading frame 2 |
| #Occurrence | 1 |
| #Paper | 1 |
| PMID | Match String | Actual String | Score | Flanking text | Edited by | Edit |
|---|---|---|---|---|---|---|
| 11679167 | nuclear encoded mitochondrial protein | nuclear encoded mitochondrial protein | 1.0 | this disorder results from a deficiency in frataxin a nuclear encoded mitochondrial protein with no homology to proteins of known function. | |