VENTXP1


Description

The VENTXP1 (VENT homeobox pseudogene 1) is a pseudo gene located on chromosome X.

VENTXP1 (VENTX/PLXDC1), also known as PLXDC1, is a protein-coding gene involved in the development of the nervous system. Its role includes axon guidance, interacting with other proteins like semaphorins and neuropilins, and exhibiting regulated expression during embryonic development. VENTXP1 is implicated in various neurological disorders, highlighting its significance in neuronal function.

VENTXP1 (VENTX/PLXDC1), also known as PLXDC1, is a protein-coding gene. It is involved in the development of the nervous system and plays a role in axon guidance. VENTXP1 interacts with other proteins, including semaphorins and neuropilins, which are key regulators of neuronal development. The gene's expression is regulated during embryonic development, particularly in the central nervous system. VENTXP1 has been linked to several neurological disorders, suggesting its critical role in neuronal function. However, further research is needed to fully understand its precise functions and potential implications in disease.

VENTXP1 is also known as CT18, NA88A, VENTX2P1.

Associated Diseases



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