Bleeding and Platelet Disorders
Gene: ANKRD26EnsemblGeneIds (GRCh38): ENSG00000107890
EnsemblGeneIds (GRCh37): ENSG00000107890
OMIM: 610855, Gene2Phenotype
ANKRD26 is in 8 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Note promoter variants.
Sources: Expert listCreated: 11 Aug 2020, 3:09 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Thrombocytopaenia 2, MIM# 188000
Publications
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Thrombocytopaenia 2, MIM# 188000
- Tags
- OMIM
- 610855
- Clinvar variants
- Variants in ANKRD26
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: ANKRD26 were changed from Thrombocytopenia 2, MIM# 188000 to Thrombocytopaenia 2, MIM# 188000
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: ankrd26 has been classified as Green List (High Evidence).
Added Tag
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Tag 5'UTR tag was added to gene: ANKRD26.
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: ankrd26 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: ANKRD26 was added gene: ANKRD26 was added to Bleeding Disorders. Sources: Expert list Mode of inheritance for gene: ANKRD26 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: ANKRD26 were set to 21211618 Phenotypes for gene: ANKRD26 were set to Thrombocytopenia 2, MIM# 188000 Review for gene: ANKRD26 was set to GREEN