STRN4
Description
The STRN4 (striatin 4) is a protein-coding gene located on chromosome 19.
Striatin-4 is a protein that in humans is encoded by the STRN4 gene.
== Interactions == STRN4 has been shown to interact with STK24.
Striatin-4 binds to calmodulin in a calcium-dependent manner, suggesting a potential role in scaffolding or signaling.
STRN4 is also known as PPP2R6C, ZIN, zinedin.
Associated Diseases
- autosomal recessive limb-girdle muscular dystrophy type 2I
- limb-girdle muscular dystrophy
- muscular dystrophy-dystroglycanopathy, type A
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
- type 1 diabetes mellitus
- cancer
- hemoglobin D disease
- retinitis pigmentosa and erythrocytic microcytosis
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- X-linked retinal dysplasia
- X-linked retinoschisis
- hemoglobin E disease
