CENTB1

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Ideogram human chromosome 17

CENTB1

CENTB1 is a protein-coding gene that plays a crucial role in cellular processes. It is located on chromosome 3 in humans and is conserved across various species. The protein encoded by CENTB1 is involved in intracellular trafficking and membrane dynamics.

Function[edit | edit source]

The primary function of CENTB1 is to regulate vesicle trafficking within cells. It interacts with other proteins and lipid molecules to facilitate the movement of vesicles between different cellular compartments. This process is essential for maintaining cellular homeostasis and proper functioning of organelles.

Structure[edit | edit source]

CENTB1 consists of multiple domains that enable its interactions with various cellular components. These domains include lipid-binding domains and protein interaction motifs. The structure of CENTB1 allows it to participate in complex signaling pathways that control vesicle trafficking.

Role in Disease[edit | edit source]

Mutations in the CENTB1 gene have been associated with certain genetic disorders. Disruption of its normal function can lead to defects in intracellular trafficking, which may contribute to the development of diseases such as neurodegenerative disorders and metabolic syndromes.

Research[edit | edit source]

Research on CENTB1 is ongoing to further understand its role in cellular processes and disease pathogenesis. Studies are focused on elucidating the specific mechanisms by which CENTB1 regulates vesicle trafficking and identifying potential therapeutic targets for related disorders.

References[edit | edit source]

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Contributors: Prab R. Tumpati, MD