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ITGB3

integrin subunit beta 3

HCNC Approved Symbol
ITGB3 (HGNC:6156)
Genomic Coordinates
17:47,253,827 - 47,313,743 (17q21.32)
Synonyms
CD61, GPIIIa, GP3A
Disease Associations
This gene is associated with the following 5 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
{Myocardial infarction, susceptibility to}
608446-
Bleeding disorder, platelet-type, 24, autosomal dominant
619271AD
Glanzmann thrombasthenia 2
619267AR
Purpura, posttransfusion
--
Thrombocytopenia, neonatal alloimmune
--

Diagnosed Cases

8Patients

In total, 8 patients were diagnosed with a variant in the ITGB3 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Abnormal bleeding
 3 (37.5%)
Prolonged bleeding time
 3 (37.5%)
Nose bleeding
 2 (25.0%)
Bleeding diathesis
 2 (25.0%)
Impaired epinephrine-induced platelet aggregation
 2 (25.0%)