NECAP2
Description
The NECAP2 (NECAP endocytosis associated 2) is a protein-coding gene located on chromosome 1.
NECAP2 is a protein encoded by the NECAP2 gene in humans. It has been shown to interact with AP1G1, a component of the adapter protein complex AP-1.
NECAP2 plays a role in the process of endocytosis, which is the uptake of molecules and particles into cells.
NECAP2 is also known as -.
Associated Diseases
- multiple sclerosis
- Parkinson disease
- Alzheimer disease
- lysosomal storage disease
- prostate cancer
- hemoglobin E-beta-thalassemia syndrome
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemoglobin D disease
- microcytic anemia with liver iron overload
- alpha thalassemia-intellectual disability syndrome type 1
- delta-beta-thalassemia
- dehydrated hereditary stomatocytosis
- dominant beta-thalassemia
- gluthathione peroxidase deficiency
- hemoglobin C-beta-thalassemia syndrome
