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 Bardet Biedl syndroom NGS Cone-rod dystrophie en macula degeneratie NGS Disorder of sex development DSD NGS Intellectual disability NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Retinitis pigmentosa NGS Visus pakket Retinale genen |