Anaemias and red cell disorders
Gene: NHP2EnsemblGeneIds (GRCh38): ENSG00000145912
EnsemblGeneIds (GRCh37): ENSG00000145912
OMIM: 606470, Gene2Phenotype
NHP2 is in 14 panels
1 review
BRIDGE consortium (NIHRBR-RD)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Dyskeratosis congenita
Publications
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- UKGTN
- Illumina TruGenome Clinical Sequencing Services
- Radboud University Medical Center, Nijmegen
- Expert list
- Phenotypes
-
- Inherited Bone Marrow Failure Syndromes
- Dyskeratosis congenita
- Dyskeratosis congenita, autosomal recessive 2, 613987
- Dyskeratosis Congenita, Recessive
- Dyskeratosis Congenita, Autosomal Recessive, 2
- DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2
- OMIM
- 606470
- Clinvar variants
- Variants in NHP2
- Penetrance
- Complete
- Panels with this gene
-
- Childhood solid tumours cancer susceptibility
- Haematological malignancies for rare disease
- Cytopenia - NOT Fanconi anaemia
- Cytopenias and congenital anaemias
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Ductal plate malformation
- Childhood solid tumours
- DDG2P
- Pulmonary fibrosis familial
- Haematological malignancies cancer susceptibility
- Rare anaemia
- Intellectual disability
- Fetal anomalies
- COVID-19 research
History Filter Activity
Added New Source
Ellen McDonagh (Genomics England Curator)NHP2 was added to Anaemias and red cell disorderspanel. Source: Radboud University Medical Center, Nijmegen NHP2 was added to Anaemias and red cell disorderspanel. Source: Illumina TruGenome Clinical Sequencing Services
Created
Ellen McDonagh (Genomics England Curator)NHP2 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)NHP2 was added to Anaemias and red cell disorderspanel. Sources: UKGTN,Expert list