HIST1H2AE


Heading: Understanding HIST1H2AE Gene: Its Role, Associated Diseases, and Latest Research

Description:

HIST1H2AE is a gene that encodes a histone protein, a structural component of DNA. It plays a crucial role in regulating gene expression by modifying the accessibility of DNA to transcription factors.

Associated Diseases:

Mutations in the HIST1H2AE gene have been linked to several genetic disorders, including:

  • Familial Dysautonomia (Riley-Day Syndrome): A rare, inherited disorder characterized by a lack of autonomic nerves, leading to severe impairments in bodily functions such as digestion, sweating, and blood pressure regulation.
  • Blepharospasm-Orofacial Dyskinesia (BOF): A neurological movement disorder that causes involuntary facial movements, including blinking and twisting.

Did you Know ?

  • Familial dysautonomia is estimated to affect approximately 1 in 370,000 individuals of Ashkenazi Jewish descent.

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.