Genes in panel
STRs in panel
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COVID-19 research

Gene: MPI

Red List (low evidence)

MPI (mannose phosphate isomerase)
EnsemblGeneIds (GRCh38): ENSG00000178802
EnsemblGeneIds (GRCh37): ENSG00000178802
OMIM: 154550, Gene2Phenotype
MPI is in 13 panels

2 reviews

Sophie Hambleton (Newcastle University)

Red List (low evidence)

I suppose the protein-losing enteropathy might cause a secondary hypogammaglobulinaemia but immunodeficiency does not appear to be a prominent aspect of the phenotype
Created: 29 Jun 2018, 2:37 p.m.

Louise Daugherty (Genomics England Curator)

Comment on list classification: Changed from Amber to Red based on external clinical expert review and review of the literature. Immunological association of this gene is not a primary phenotype and is better represented on other panels (Congenital disorders of glycosylation, Undiagnosed metabolic disorders, Intellectual disability). Gene is pertinent on Victorian Clinical Genetics Services panel for Immunological disorders. However gene not present on any other PID related panels or within ESID or IUIS classifications. Request evidences / immunological association of this gene from Victorian Clinical Genetics Services.
Created: 4 Jul 2018, 12:59 p.m.
Comment on list classification: This gene was absent from the original PanelApp PID panel dataset (review April 2018). However it was listed in external expert immunodeficiency diagnostic gene list from Victorian Clinical Genetics Services. In this combined PID panel, this gene has been rated as AMBER and needs further curational review to assess pertinence prior to v1. No disorder or MOI was listed in the submitted list.
Created: 26 Jun 2018, 12:46 p.m.


Mode of Inheritance
  • Victorian Clinical Genetics Services
  • Expert Review Red
  • Expert Review Red
  • Victorian Clinical Genetics Services
  • Congenital disorder of glycosylation, type Ib, OMIM:602579
  • MPI-CDG, MONDO:0011257
Clinvar variants
Variants in MPI
Panels with this gene

History Filter Activity

24 Dec 2020, Gel status: 1

Set Phenotypes

Arina Puzriakova (Genomics England Curator)

Phenotypes for gene: MPI were changed from to Congenital disorder of glycosylation, type Ib, OMIM:602579; MPI-CDG, MONDO:0011257

1 Apr 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance

Ellen McDonagh (Genomics England Curator)

gene: MPI was added gene: MPI was added to Viral susceptibility. Sources: Expert Review Red,Victorian Clinical Genetics Services Mode of inheritance for gene: MPI was set to Unknown