Inherited ovarian cancer (without breast cancer)
Gene: NBNEnsemblGeneIds (GRCh38): ENSG00000104320
EnsemblGeneIds (GRCh37): ENSG00000104320
OMIM: 602667, Gene2Phenotype
NBN is in 25 panels
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Details
- Sources
-
- Emory Genetics Laboratory
- Phenotypes
-
- Breast and Ovarian Cancer
- OMIM
- 602667
- Clinvar variants
- Variants in NBN
- Penetrance
- Complete
- Panels with this gene
-
- Fetal anomalies
- Clefting
- Childhood solid tumours cancer susceptibility
- Inherited ovarian cancer (without breast cancer)
- Familial breast cancer
- Cytopenia - NOT Fanconi anaemia
- Monogenic short stature
- Haematological malignancies cancer susceptibility
- Familial Tumours Syndromes of the central & peripheral Nervous system
- Severe microcephaly
- Sarcoma cancer susceptibility
- Cytopenias and congenital anaemias
- Primary ovarian insufficiency
- Osteogenesis imperfecta
- COVID-19 research
- Familial rhabdomyosarcoma
- Haematological malignancies for rare disease
- Intellectual disability
- Sarcoma susceptibility
- Sarcoma of possible germline origin
- DDG2P
- Primary immunodeficiency or monogenic inflammatory bowel disease
- IUGR and IGF abnormalities
- Nijmegen breakage syndrome
- Childhood solid tumours
History Filter Activity
panel promoted to version 1
Ellen McDonagh (Genomics England Curator)31/07/2017: Promoted panel to version 1, after checking against the original list sent by Clare Turnbull for this panel.
Added New Source
Ellen McDonagh (Genomics England Curator)NBN was added to Familial ovarian cancerpanel. Sources: Emory Genetics Laboratory
Created
Ellen McDonagh (Genomics England Curator)NBN was created by ellenmcdonagh