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IBMDx study

Gene: ANKRD26

Green List (high evidence)
ANKRD26 (ankyrin repeat domain 26)
EnsemblGeneIds (GRCh38): ENSG00000107890
EnsemblGeneIds (GRCh37): ENSG00000107890
OMIM: 610855, Gene2Phenotype
ANKRD26 is in 8 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Note promoter variants.
Created: 15 Jun 2021, 10:04 a.m. | Last Modified: 15 Jun 2021, 10:04 a.m.
Panel Version: 0.227

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Thrombocytopaenia 2, MIM# 188000

Publications

Created: 15 Jun 2021, 10:04 a.m.
Last Modified: 15 Jun 2021, 10:04 a.m.
Panel version: Imported from Bone Marrow Failure panel version 0.227

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Green
  • IBMDx Study
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Thrombocytopaenia 2, MIM# 188000
OMIM
610855
Clinvar variants
Variants in ANKRD26
Penetrance
None
Panels with this gene

History Filter Activity

10 Dec 2021, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: ANKRD26 was added gene: ANKRD26 was added to IBMDx study. Sources: IBMDx Study,Expert Review Green Mode of inheritance for gene: ANKRD26 was set to Unknown Phenotypes for gene: ANKRD26 were set to Thrombocytopaenia 2, MIM# 188000