nbn gene | NBN gene: MedlinePlus Genetics

Keyword	CPC	PCC	Volume	Score	Length of keyword
nbn gene	1.93	0.5	2491	54	8
nbn	0.14	0.9	6016	56	3
gene	1.89	0.5	1557	28	4

Keyword	CPC	PCC	Volume	Score
nbn gene	1.52	0.1	685	85
nbn gene mutation	0.64	1	4549	61
nbn gene cancer risks	0.66	0.5	9146	42
nbn gene reviews	1.15	0.5	4445	65
nbn gene breast cancer	0.46	0.1	3889	93
nbn general trading llc	0.71	0.9	1121	72
nbn gene variant	1	0.3	2758	86
nbn gene positive	1.06	0.8	4479	81
nbn general counsel	1.27	0.8	3528	100
nbn genetic testing	0.83	1	4537	39
nbn gene mutation cancer risk	1.12	0.6	6408	94
nbn gene mutation icd 10	1.45	0.3	4698	1
nbn gene mutation and breast cancer	1.85	0.9	7061	49
nbn genetic mutation	0.97	1	1484	17
what is the nbn gene	0.92	0.1	228	38

Search Results related to nbn gene on Search Engine

NBN gene: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/gene/nbn/

WEBThe 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 two other proteins, produced from the MRE11A and RAD50 genes, as part of a larger protein complex.

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NBN Gene - GeneCards | NBN Protein | NBN Antibody
genecards.org

https://www.genecards.org/cgi-bin/carddisp.pl?gene=NBN

WEBApr 3, 2024 · GeneCards Summary for NBN Gene. NBN (Nibrin) is a Protein Coding gene. Diseases associated with NBN include Nijmegen Breakage Syndrome and Aplastic Anemia . Among its related pathways are Homologous DNA Pairing and Strand Exchange and Resolution of D-loop Structures through Holliday Junction Intermediates .

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NBN Inherited Mutations - Overview of NBN gene mutations
facingourrisk.org

https://www.facingourrisk.org/hereditary-cancer-genes-and-risk/NBN-risks-prevention-treatment

WEBFeb 25, 2024 · People who inherit a mutation in both copies of their NBN gene—one from each parent—have a rare disease known as Nijmegen breakage syndrome. People with Nijmegen breakage syndrome can have multiple serious health problems and an increased risk for certain cancers.

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NBN - My Cancer Genome
mycancergenome.org

https://www.mycancergenome.org/content/gene/nbn/

WEBNibrin (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 mutations, silent mutations, frameshift deletions, and nonsense mutations are observed in cancers such as colon cancer, stomach cancer, and endometrial cancer.

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Nijmegen breakage syndrome: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/condition/nijmegen-breakage-syndrome/

WEBMutations in the NBN gene cause Nijmegen breakage syndrome. 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.

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Nibrin - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Nibrin

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

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NBN nibrin [Homo sapiens (human)] - Gene - NCBI
nih.gov

https://www.ncbi.nlm.nih.gov/gene?Cmd=DetailsSearch&Term=4683

WEBMar 5, 2024 · NBN nibrin [Homo sapiens (human)] - Gene - NCBI. NBN nibrin [ Homo sapiens (human) ] Gene ID: 4683, updated on 5-Mar-2024. Download Datasets. Summary. Official Symbol. NBN provided by HGNC. Official Full Name. nibrin provided by HGNC. Primary source. HGNC:HGNC:7652. See related. Ensembl:ENSG00000104320 …

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Association of the nibrin gene (NBN) variants with breast cancer
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774354/

WEBJan 25, 2016 · Nibrin, encoded by the NBN gene, participates in DNA repair. Mutations in the NBN gene lead to Nijemen breakage syndrome, which may result in several types of diseases, particularly susceptibility to cancer, including breast cancer.

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NBN gene - MedlinePlus
medlineplus.gov

https://medlineplus.gov/download/genetics/gene/nbn.pdf

WEBThe 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 two other proteins, produced from the MRE11A and RAD50 genes, as part of a larger protein complex. Nibrin regulates the activity of this complex by ...

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4683 - Gene ResultNBN nibrin [ (human)] - National Center for
nih.gov

https://www.ncbi.nlm.nih.gov/gene/4683

WEBNBN gene product nibrin plays an important role at different levels in the B-cell system and in the pathology of the Nijmegen breakage syndrome. Results suggest an important role of NBN 1197A>G and XRCC3-316A>G polymorphisms in the development of second neoplasm in patients treated for childhood acute lymphoblastic leukemia (ALL).

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