| Approved symbol | MKKS |
|---|---|
| Approved name | MKKS centrosomal shuttling protein |
| HGCN ID | HGNC:7108 |
| Previous symbols | BBS6 |
| Inheritance | |
| OMIM | 604896 |
| Chromosome | 20p12.2 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Disorder of sex development DSD NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
