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Newborns main panel

Gene: CR2

Amber List (moderate evidence)

CR2 (complement C3d receptor 2)
EnsemblGeneIds (GRCh38): ENSG00000117322
EnsemblGeneIds (GRCh37): ENSG00000117322
OMIM: 120650, Gene2Phenotype
CR2 is in 2 panels

1 review

Mafalda Gomes (Genomics England Curator)

The mechanism of pathogenicity is loss-of-function (LOF).
Created: 1 Jun 2023, 2:40 p.m. | Last Modified: 1 Jun 2023, 2:40 p.m.
Panel Version: 0.137
CR2 curation results (clinicalgenome.org)
Created: 1 Jun 2023, 12:22 p.m. | Last Modified: 1 Jun 2023, 12:22 p.m.
Panel Version: 0.134

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
Phenotypes
  • Common variable immune deficiency 7
OMIM
120650
Clinvar variants
Variants in CR2
Penetrance
None
Panels with this gene

History Filter Activity

14 Sep 2023, Gel status: 2

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Amber was added to CR2. Added phenotypes Common variable immune deficiency 7 for gene: CR2 Rating Changed from Green List (high evidence) to Amber List (moderate evidence)

5 Jul 2023, Gel status: 3

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Green was added to CR2. Added phenotypes Common variable immune deficiency 7 for gene: CR2 Rating Changed from Amber List (moderate evidence) to Green List (high evidence)

31 May 2023, Gel status: 2

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Amber was added to CR2. Added phenotypes Common variable immune deficiency 7 for gene: CR2 Rating Changed from Green List (high evidence) to Amber List (moderate evidence)

15 May 2023, Gel status: 3

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Green was added to CR2. Added phenotypes Common variable immune deficiency 7 for gene: CR2 Rating Changed from No List (delete) to Green List (high evidence)

9 Mar 2023, Gel status: 0

Created, Added New Source, Set mode of inheritance

Mafalda Gomes (Genomics England Curator)

gene: CR2 was added gene: CR2 was added to Newborns main panel. Sources: Expert Review Removed Mode of inheritance for gene: CR2 was set to BIALLELIC, autosomal or pseudoautosomal