HLX (gene)

HLX (H2.0-like homeobox) is a gene that in humans is encoded by the HLX gene. HLX is a member of the homeobox family of genes, which are critical for body planning during embryonic development.

Function

The HLX gene is a transcription factor that plays a significant role in the regulation of cell proliferation and differentiation. It is expressed in a variety of tissues, including the brain, liver, and kidney. The protein encoded by this gene is a nuclear protein, suggesting that it may have a role in the regulation of gene expression.

Clinical significance

Mutations in the HLX gene have been associated with a variety of diseases, including cancer, autoimmune diseases, and developmental disorders. For example, overexpression of HLX has been observed in leukemia and other types of cancer, suggesting that it may play a role in tumorigenesis.

Research

Research into the HLX gene is ongoing, with scientists seeking to better understand its function and the role it plays in disease. This research could potentially lead to new treatments for diseases associated with mutations in the HLX gene.

See also

• Homeobox
• Transcription factor
• Gene expression
• Cell proliferation
• Cell differentiation

External links

• HLX at the National Center for Biotechnology Information
• HLX at the Genetics Home Reference

‎

---

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