Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organization.
- Cited forVARIANT TYR-148, FUNCTION, SUBCELLULAR LOCATION, CHARACTERIZATION OF VARIANT TYR-148, CHROMOSOMAL TRANSLOCATION
- CategoriesFunction, Sequences, Disease & Variants, Subcellular Location
- SourceUniProtKB reviewed (Swiss-Prot)