FKSG29

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Description

The FKSG29 (-) is a ncRNA gene located on chromosome 13.

FKSG29 is a human gene located on chromosome 10. It encodes a protein with a conserved domain structure, suggesting potential involvement in protein binding and cellular functions. However, its precise role and mechanism of action are currently unknown and require further investigation.

The precise function of FKSG29 remains unclear, with limited research available. However, its protein structure hints at potential involvement in protein binding and cellular processes, suggesting a role in maintaining cellular homeostasis and function.

FKSG29 is also known as -.

Associated Diseases