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  3. HOXA11
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IBMDx study

Gene: HOXA11

Green List (high evidence)
HOXA11 (homeobox A11)
EnsemblGeneIds (GRCh38): ENSG00000005073
EnsemblGeneIds (GRCh37): ENSG00000005073
OMIM: 142958, Gene2Phenotype
HOXA11 is in 6 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

I don't know

Radioulnar synostosis with amegakaryocytic thrombocytopenia (RUSAT) is characterized by thrombocytopenia that progresses to pancytopenia, in association with congenital proximal fusion of the radius and ulna that results in extremely limited pronation and supination of the forearm. Two families reported in 2000, segregating same variant. No further reports since.
Created: 14 Sep 2020, 12:08 a.m. | Last Modified: 14 Sep 2020, 12:08 a.m.
Panel Version: 0.98

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MIM# 605432

Publications

Created: 14 Sep 2020, 12:08 a.m.
Last Modified: 14 Sep 2020, 12:08 a.m.
Panel version: Imported from Bone Marrow Failure panel version 0.102

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Green
  • IBMDx Study
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MIM# 605432
OMIM
142958
Clinvar variants
Variants in HOXA11
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: HOXA11 was added gene: HOXA11 was added to IBMDx study. Sources: IBMDx Study,Expert Review Green Mode of inheritance for gene: HOXA11 was set to Unknown Phenotypes for gene: HOXA11 were set to Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MIM# 605432