The NBN gene provides instructions for making a protein called nibrin. This protein is involved in several critical cellular functions, including the repair of damaged DNA. Nibrin interacts with …

2025年3月30日 · NBN (Nibrin) is a Protein Coding gene. Diseases associated with NBN include Nijmegen Breakage Syndrome and Aplastic Anemia. Among its related pathways are …

Nibrin, also known as NBN or NBS1, is a protein which in humans is encoded by the NBN gene. [5][6][7] Nibrin is a protein associated with the repair of double strand breaks (DSBs) which …

2025年3月24日 · An inherited NBN mutation may affect your options for cancer prevention, detection and treatment. FORCE is here to guide you.

2021年11月30日 · Title: XRCC3 and NBS1 gene polymorphisms modulate the risk of pre-oral cancer and oral cancer in the North Indian population. The NBN founder mutation-Evidence for …

2023年12月20日 · The Nbn gene, also known as Nibrin gene, is a gene that is involved in DNA repair and maintenance of genomic stability. The expression, structure, and function of the …

The NBN gene provides instructions for making a protein called nibrin. This protein is involved in several critical cellular functions, including the repair of damaged DNA. Nibrin interacts with …

NBN . gene has two main jobs. The first is to help fix DNA when it is damaged. The second is to help prevent cancer from forming. If you have a mutation in one copy of the . NBN . gene, it …

Gene ID: 4683, updated on 8-Feb-2025. Mutations in this gene are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized …

Nibrin (NBN) is a gene that encodes a protein that is a member of the MRE11/RAD50 double-strand break repair complex and is associated with Nijmegen breakage syndrome. Missense …