SOX9

SOX9 is a transcription factor that plays a critical role in the regulation of development and cell differentiation. It is encoded by the SOX9 gene in humans.

Function

SOX9 is a member of the SOX gene family, which is characterized by the presence of a High-Mobility Group (HMG) domain. This domain enables the protein to bind to the DNA and regulate the activity of other genes. SOX9 is particularly important in the development of the testes and the formation of cartilage.

Clinical significance

Mutations in the SOX9 gene can lead to a variety of medical conditions. For example, Campomelic dysplasia, a severe form of dwarfism, is often caused by mutations in this gene. Additionally, SOX9 mutations have been associated with 46,XX testicular DSD, a condition in which individuals with two X chromosomes develop testes.

Research

Research on SOX9 has provided valuable insights into the processes of cell differentiation and organogenesis. It has also contributed to our understanding of certain genetic disorders and may eventually lead to new therapeutic strategies for these conditions.

See also

• SOX gene family
• Transcription factor
• Campomelic dysplasia
• 46,XX testicular DSD

References

‎

---

Translate: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, தமிழ், తెలుగు, Urdu, ಕನ್ನಡ, Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, বাংলা
European español, Deutsch, français, Greek, português do Brasil, polski, română, русский, Nederlands, norsk, svenska, suomi, Italian
Middle Eastern & African عربى, Turkish, Persian, Hebrew, Afrikaans, isiZulu, Kiswahili,
Other Bulgarian, Hungarian, Czech, Swedish, മലയാളം, मराठी, ਪੰਜਾਬੀ, ગુજરાતી, Portuguese, Ukrainian