| GENE NAME | TTC21B |
| CHROMOSOME | 2 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000123607 |
| UNIPROT ACCESSION NUMBER | Q7Z4L5 |
| GO MOLECULAR FUNCTION | ['chromatin binding', 'protein binding'] |
| ESSENTIAL IN MOUSE | Non-essential |
| PATHWAYS | R-HSA-162582; R-HSA-1852241; R-HSA-5358351; R-HSA-5610787; R-HSA-5617833; R-HSA-5620924 |
| 1 combination linked to TTC21B | OLI1741 |
| 1 variant linked to TTC21B | TTC21B:c.2258C>T, p.Pro753Leu |
| 1 disease linked to TTC21B | Congenital hydrocephalus |