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Mendeliome

Gene: TIRAP

Red List (low evidence)

TIRAP (TIR domain containing adaptor protein)
EnsemblGeneIds (GRCh38): ENSG00000150455
EnsemblGeneIds (GRCh37): ENSG00000150455
OMIM: 606252, Gene2Phenotype
TIRAP is in 2 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

No evidence currently for Mendelian disease association. Some evidence for polymorphisms in this gene influencing susceptibility/protection from infectious disease. One family with 8 individuals and bi-allelic variants and susceptibility to staphylococcal disease reported.
Created: 20 Nov 2019, 10:17 a.m. | Last Modified: 5 Apr 2020, 8:55 a.m.
Panel Version: 0.1987

Mode of inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal

Publications

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
606252
Clinvar variants
Variants in TIRAP
Penetrance
None
Panels with this gene

History Filter Activity

20 Nov 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

20 Nov 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: tirap 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: TIRAP was added gene: TIRAP was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: TIRAP was set to Unknown