EMB
Description
The Emb gene, also known as the Embryonic lethal, abnormal vision (emb) gene, plays a crucial role in the development of various tissues and organs during embryonic development. This gene encodes a transcription factor, a protein that regulates the expression of other genes, and is essential for the proper formation of the nervous system, eyes, and other structures. Mutations in the Emb gene can lead to severe developmental abnormalities and embryonic lethality. While initially studied in the context of embryonic development, research has revealed that the Emb gene also plays a role in adult tissues and may be involved in various physiological processes.
Associated Diseases
- Microphthalmia (small eyes)
- Anophthalmia (absence of eyes)
- Neural tube defects
- Craniofacial abnormalities
Did you know?
The Emb gene is highly conserved across different species, suggesting its fundamental importance in developmental biology.
