JAG1 : jagged canonical Notch ligand 1


Jagged-1: A Pivotal Player in Cell Signaling and Development

Description

The JAG1 gene holds the blueprint for creating a protein called Jagged-1, a crucial player in the intricate dance of cell communication known as the Notch signaling pathway. Jagged-1, a membrane-bound protein, serves as a "lock" that invites Notch receptors, found on neighboring cells, to connect like a "key."

Associated Diseases

Jagged-1‘s involvement in embryonic development and cell regulation extends its significance to various diseases:

  • Alagille Syndrome: A rare inherited disorder characterized by liver and heart defects. Mutations in the JAG1 gene disrupt Notch signaling, hindering proper development.
  • Tetralogy of Fallot: A heart condition where oxygen-poor blood flows to the body. Abnormal Jagged-1 expression has been linked to its occurrence.
  • Spinocerebellar Ataxia Type 2: A progressive neurological disorder affecting coordination and balance. Mutations in JAG1 impair the development of the nervous system.

Did you Know ?

Jagged-1‘s importance is evident in its prevalence: approximately 1 in 100,000 people worldwide suffer from Alagille Syndrome caused by mutations in JAG1. This statistic highlights the profound impact of Jagged-1 on human health.


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.