TIMELESS


The Timeless Gene: A Journey into the Eternal

Description

The TIMELESS gene, located on chromosome 15q25, encodes a protein essential for maintaining the delicate balance of the cell cycle. It acts as a molecular checkpoint, ensuring that cells progress through the various phases of division in a timely and orderly manner.

Associated Diseases

Mutations in the TIMELESS gene have been linked to several developmental disorders, including:

  • Microcephaly: A condition characterized by an abnormally small head and brain size.
  • Short stature: A condition where individuals are significantly shorter than the average height.
  • Craniofacial abnormalities: Developmental malformations of the skull and face, such as cleft lip and palate.
  • Intellectual disability: Cognitive impairments affecting learning, memory, and problem-solving abilities.

Did you Know ?

Researchers have estimated that mutations in the TIMELESS gene are present in approximately 1 in 200,000 individuals worldwide. This highlights the rarity and significance of these mutations.



Disclaimer: The information provided here is not exhaustive by any means. Always consult your doctor or other qualified healthcare provider with any questions you may have regarding a medical condition, procedure, or treatment, whether it is a prescription medication, over-the-counter drug, vitamin, supplement, or herbal alternative.