| Entrez Gene ID | 168448 |
|---|---|
| Official Gene Symbol | CDC14C (GeneCards) |
| Full name | cell division cycle 14C |
| Location | 7p12.3 |
| Other ids | HGNC : HGNC:22427 |
| Other names | CDC14B2, CDC14Bretro |
| Summary | This gene represents a retrogene of cell division cycle 14B (CDC14B), which is located on chromosome 9. The introns in the coding sequence have been processed out relative to the CDC14B locus, but there is an intact open reading frame that is missing only some sequence at the N-terminus, including the nuclear localiztion signal, relative to proteins encoded by the CDC14B gene. There is a difference in the subcellular localization of the protein encoded by this gene, relative to its parental gene product. While the parental gene product displays microtubular localization, GFP chimeras of the protein encoded by this gene localize to the endoplasmic reticulum, indicating a possible new functional role for this gene. [provided by RefSeq, Nov 2017] |
Found 8 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 10406 | 168448 | CDC14C | 7 | 49352216 | 49352216 | Asymptomatic | HiSeq X Ten |
| 10434 | 168448 | CDC14C | 7 | 49727514 | 49727514 | Asymptomatic | HiSeq X Ten |
| 10915 | 168448 | CDC14C | 7 | 49567893 | 49567893 | Asymptomatic | HiSeq X Ten |
| 10916 | 168448 | CDC14C | 7 | 49706597 | 49706597 | Asymptomatic | HiSeq X Ten |
| 11306 | 168448 | CDC14C | 7 | 49295187 | 49295187 | Asymptomatic | HiSeq X Ten |
| 11363 | 168448 | CDC14C | 7 | 49611752 | 49611752 | Cockayne syndrome | HiSeq X Ten |
| 11373 | 168448 | CDC14C | 7 | 49541421 | 49541421 | Cockayne syndrome | HiSeq X Ten |
| 23202 | 168448 | CDC14C | 7 | 49255503 | 49255503 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |