Approved symbol | SNX10 |
---|---|
Approved name | sorting nexin 10 |
HGCN ID | HGNC:14974 |
Previous symbols | |
Inheritance | |
OMIM | 614780 |
Chromosome | 7p15.2 |
Panel(s) |
NGS Mendeliome NGS Osteopetrosis and dense bone dysplasia NGS Preconception panel (for consanguineous couples) NGS Primary immunodeficiency PID NGS Skeletal Dysplasia |