This Panel is marked as Internal
Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuria
Gene: PALB2
PALB2 (partner and localizer of BRCA2)
EnsemblGeneIds (GRCh38): ENSG00000083093
EnsemblGeneIds (GRCh37): ENSG00000083093
OMIM: 610355, Gene2Phenotype
PALB2 is in 26 panels
EnsemblGeneIds (GRCh38): ENSG00000083093
EnsemblGeneIds (GRCh37): ENSG00000083093
OMIM: 610355, Gene2Phenotype
PALB2 is in 26 panels
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Details
- Sources
-
- Expert list
- Phenotypes
-
- Fanconi anemia
- OMIM
- 610355
- Clinvar variants
- Variants in PALB2
- Penetrance
- Complete
- Panels with this gene
-
- Childhood solid tumours cancer susceptibility
- Radial dysplasia
- Familial breast cancer
- Haematological malignancies cancer susceptibility
- Familial Tumours Syndromes of the central & peripheral Nervous system
- DDG2P
- Cytopenias and congenital anaemias
- Intellectual disability
- COVID-19 research
- Inherited ovarian cancer (without breast cancer)
- Neurofibromatosis Type 1
- Breast cancer pertinent cancer susceptibility
- Limb disorders
- Haematological malignancies for rare disease
- Adult solid tumours for rare disease
- Fetal anomalies
- Familial prostate cancer
- Inherited breast cancer and ovarian cancer
- Severe microcephaly
- Pigmentary skin disorders
- Inherited prostate cancer
- Adult solid tumours cancer susceptibility
- Monogenic short stature
- Childhood solid tumours
- Inherited pancreatic cancer
- Confirmed Fanconi anaemia or Bloom syndrome
History Filter Activity
19 Nov 2015, Gel status: 0
Created
Ellen McDonagh (Genomics England Curator)PALB2 was created by ellenmcdonagh
19 Nov 2015, Gel status: 0
Added New Source
Ellen McDonagh (Genomics England Curator)PALB2 was added to Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuriapanel. Sources: Expert list