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Newborns main panel

Gene: ITGB3

Green List (high evidence)

ITGB3 (integrin subunit beta 3)
EnsemblGeneIds (GRCh38): ENSG00000259207
EnsemblGeneIds (GRCh37): ENSG00000259207
OMIM: 173470, Gene2Phenotype
ITGB3 is in 6 panels

2 reviews

Arina Puzriakova (Genomics England Curator)

Special Consideration: VCEP - a ClinGen Variant Review Expert Panel (VCEP) has produced specifications to the ACMP/AMP variant interpretation guidelines for this gene.

Additional Information: Link to Platelet Disorders Variant Curation Expert Panel (VCEP) - https://www.clinicalgenome.org/affiliation/50040/
Created: 26 Sep 2024, 3:29 p.m. | Last Modified: 26 Sep 2024, 3:29 p.m.
Panel Version: 0.469

Mafalda Gomes (Genomics England Curator)

The mechanism of pathogenicity is loss-of-function (LOF).
Created: 1 Jun 2023, 2:40 p.m. | Last Modified: 1 Jun 2023, 2:40 p.m.
Panel Version: 0.137
ITGB3 curation results (clinicalgenome.org)
Created: 1 Jun 2023, 12:22 p.m. | Last Modified: 1 Jun 2023, 12:22 p.m.
Panel Version: 0.134

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • Glanzmann thrombasthenia 2
Tags
special_consideration
OMIM
173470
Clinvar variants
Variants in ITGB3
Penetrance
None
Panels with this gene

History Filter Activity

26 Sep 2024, Gel status: 3

Added Tag

Arina Puzriakova (Genomics England Curator)

Tag special_consideration tag was added to gene: ITGB3.

14 Sep 2023, Gel status: 3

Set Phenotypes

Mafalda Gomes (Genomics England Curator)

Added phenotypes Glanzmann thrombasthenia 2 for gene: ITGB3

5 Jul 2023, Gel status: 3

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Green was added to ITGB3. Added phenotypes Glanzmann thrombasthenia 2 for gene: ITGB3 Rating Changed from Amber List (moderate evidence) to Green List (high evidence)

31 May 2023, Gel status: 2

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

Mafalda Gomes (Genomics England Curator)

gene: ITGB3 was added gene: ITGB3 was added to Newborns main panel. Sources: Expert Review Amber Mode of inheritance for gene: ITGB3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ITGB3 were set to Glanzmann thrombasthenia 2