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COVID-19 research

Gene: IL31RA

Red List (low evidence)

IL31RA (interleukin 31 receptor A)
EnsemblGeneIds (GRCh38): ENSG00000164509
EnsemblGeneIds (GRCh37): ENSG00000164509
OMIM: 609510, Gene2Phenotype
IL31RA is in 4 panels

1 review

Louise Daugherty (Genomics England Curator)

Not clearly a primary immunodeficiency. New gene added after review of potential new genes for PID by the Immunology Test Group. This gene was noted as being only theoretical for PID so was rated as Red by the group.
Created: 27 Sep 2019, 2:42 p.m. | Last Modified: 27 Sep 2019, 2:47 p.m.
Panel Version: 1.132

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
Phenotypes
  • ?Amyloidosis, primary localized cutaneous 2, 613955
OMIM
609510
Clinvar variants
Variants in IL31RA
Penetrance
None
Panels with this gene

History Filter Activity

1 Apr 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: IL31RA was added gene: IL31RA was added to Viral susceptibility. Sources: Expert Review Red,NHS GMS,London North GLH Mode of inheritance for gene: IL31RA was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: IL31RA were set to ?Amyloidosis, primary localized cutaneous 2, 613955