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Severe Paediatric Disorders

Gene: FPR1

Red List (low evidence)

FPR1 (formyl peptide receptor 1)
EnsemblGeneIds (GRCh38): ENSG00000171051
EnsemblGeneIds (GRCh37): ENSG00000171051
OMIM: 136537, Gene2Phenotype
FPR1 is in 3 panels

1 review

Louise Daugherty (Genomics England Curator)

I don't know

Initial gene list (NGC_genelist-20190823_GREEN_dis_moi_forCuration_20200211.xlsx) collated by Dr Courtney French (University of Cambridge University Hospital NHS Foundation), Dr Karyn Megy (Clinical Feedback Lead, NIHR BioResource - Rare Diseases Study, University of Cambridge University Hospital NHS Foundation), Dr Alba Sanchis-Juan (NIHR BioResource - Rare Diseases Study, University of Cambridge University Hospital NHS Foundation) and Lucy Raymond (Professor of Medical Genetics and Neurodevelopment, University of Cambridge University Hospital NHS Foundation). Submitted to the PanelApp resource January 2020 on behalf of the Next Generation Children Project, Addenbrookes' Hospital, Cambridge. Gene Symbol submitted: FPR1; Recommended initial gene rating: Red List (low evidence); Phenotypes: ; Mode of inheritance:
Created: 20 Feb 2020, 5:28 p.m. | Last Modified: 20 Feb 2020, 5:28 p.m.
Panel Version: 0.12

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Next Generation Children Project
  • Expert Review Red
  • Expert list
OMIM
136537
Clinvar variants
Variants in FPR1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 Feb 2020, Gel status: 1

Set publications

Louise Daugherty (Genomics England Curator)

Publications for gene FPR1 were updated from to 30847515

19 Feb 2020, Gel status: 1

Set mode of inheritance

Louise Daugherty (Genomics England Curator)

Mode of inheritance for gene FPR1 was changed from to BIALLELIC, autosomal or pseudoautosomal

14 Feb 2020, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source Next Generation Children Project was added to FPR1.