Vasculitis
Gene: TAP2EnsemblGeneIds (GRCh38): ENSG00000204267
EnsemblGeneIds (GRCh37): ENSG00000204267
OMIM: 170261, Gene2Phenotype
TAP2 is in 3 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
5 individuals from 4 unrelated families reported with TAP2 variants resulting in BLS type 1; two mouse models
Homozygous missense variants resulting in premature stop codons were identified.
Individuals typically presented with recurrent respiratory bacterial infections and reduced CD8+ cells with granulomatous lesions and/or skin vasculitis.
Sources: Expert ReviewCreated: 17 Aug 2021, 8:08 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bare lymphocyte syndrome, type I, due to TAP2 deficiency MIM# 604571; Low CD8; absent MHC I on lymphocytes; Vasculitis; pyoderma gangrenosum; recurrent bacterial/viral respiratory infections; bronchiectasis
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Expert Review
- Phenotypes
-
- Bare lymphocyte syndrome, type I, due to TAP2 deficiency MIM# 604571
- Low CD8
- absent MHC I on lymphocytes
- Vasculitis
- pyoderma gangrenosum
- recurrent bacterial/viral respiratory infections
- bronchiectasis
- OMIM
- 170261
- Clinvar variants
- Variants in TAP2
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: tap2 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: tap2 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: TAP2 was added gene: TAP2 was added to Vasculitis. Sources: Expert Review Mode of inheritance for gene: TAP2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TAP2 were set to 7517574; 9232449; 10560675; 27861817 Phenotypes for gene: TAP2 were set to Bare lymphocyte syndrome, type I, due to TAP2 deficiency MIM# 604571; Low CD8; absent MHC I on lymphocytes; Vasculitis; pyoderma gangrenosum; recurrent bacterial/viral respiratory infections; bronchiectasis Review for gene: TAP2 was set to GREEN