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  3. FPR1
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Phagocyte Defects

Gene: FPR1

Red List (low evidence)
FPR1 (formyl peptide receptor 1)
EnsemblGeneIds (GRCh38): ENSG00000171051
EnsemblGeneIds (GRCh37): ENSG00000171051
OMIM: 136537, Gene2Phenotype
FPR1 is in 2 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Possible link with periodontitis. A lot of experimental data but link to human monogenic disease unclear.
Created: 10 Apr 2020, 7:33 a.m. | Last Modified: 10 Apr 2020, 7:33 a.m.
Panel Version: 0.32

Phenotypes
Periodontitis

Publications

Created: 10 Apr 2020, 7:33 a.m.
Last Modified: 10 Apr 2020, 7:33 a.m.
Panel version: 0.32

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Melbourne Genomics Health Alliance Immunology Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Periodontitis
OMIM
136537
Clinvar variants
Variants in FPR1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

10 Apr 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: fpr1 has been classified as Red List (Low Evidence).

10 Apr 2020, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: FPR1 were changed from to Periodontitis

10 Apr 2020, Gel status: 1

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: FPR1 were set to

10 Apr 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: fpr1 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: FPR1 was added gene: FPR1 was added to Phagocyte defects_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship Mode of inheritance for gene: FPR1 was set to Unknown