| Approved symbol | MKS1 |
|---|---|
| Approved name | MKS transition zone complex subunit 1 |
| HGCN ID | HGNC:7121 |
| Previous symbols | MKS |
| Inheritance | |
| OMIM | 609883 |
| Chromosome | 17q22 |
| Panel(s) |
NGS Bardet Biedl syndrome NGS Cone-rod dystrophy and macula degeneration NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
