CTTNBP2NL
Description
The CTTNBP2NL (CTTNBP2 N-terminal like) is a protein-coding gene located on chromosome 1.
CTTNBP2 N-terminal-like protein is a protein that in humans is encoded by the CTTNBP2NL gene. It is a substrate for phosphorylation. It has been shown to interact with other proteins.
Plays a role in regulating the movement and organization of actin filaments in cell protrusions called lamellipodia, which are important for cell migration. This regulation is dependent on its interaction with the protein CTTN (cortactin).
CTTNBP2NL is also known as -.
Associated Diseases
- hemoglobin D disease
- hemoglobin E-beta-thalassemia syndrome
- dominant beta-thalassemia
- hemoglobin E disease
- delta-beta-thalassemia
- hemoglobin C-beta-thalassemia syndrome
- alpha-thalassemia-myelodysplastic syndrome
- hemoglobin H disease
- tuberculosis
- pancreatic ductal adenocarcinoma
- cancer
