NECAP2

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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