FAM120C

FAM120C is a human gene. Its full name is Family With Sequence Similarity 120, Member C. It is located on chromosome 7 in humans.

Gene Function and Characteristics:

The precise function of FAM120C is not yet fully elucidated, but it is believed to play a role in cellular processes. Research suggests it may be involved in processes related to cell growth, differentiation, or signal transduction. Further investigation is needed to fully understand its biological role. The protein encoded by this gene has been observed to interact with other proteins within the cell.

Related Diseases/Conditions:

While specific diseases directly linked to mutations or dysregulation of the FAM120C gene are not definitively established, variations in its expression or structure could potentially contribute to the development of certain conditions. Ongoing research is investigating potential associations between FAM120C and various diseases.

Further Research:

Continued research is crucial to fully understanding the function of FAM120C and its potential role in health and disease. This includes studies focused on:

• Identifying specific protein interactions of FAM120C.
• Determining the precise cellular pathways in which FAM120C participates.
• Investigating the effects of FAM120C mutations on cellular function and organismal health.
• Exploring potential therapeutic applications related to FAM120C modulation.

External Links:

(Links to reputable databases such as NCBI Gene, UniProt, and Ensembl would be included here in a complete wiki entry.)