platelet-type bleeding disorder 11

Summary
Synonym
  • BDPLT11
  • GP VI deficiency
  • glycoprotein VI deficiency
Definition
A blood platelet disease characterized by autosomal recessive inheritance of mild to moderate bleeding and defective platelet activation and aggregation in response to collagen that has_material_basis_in compound heterozygous mutation in the GP6 gene on chromosome 19q13.
Super Class
autosomal recessive disease blood platelet disease
External Links
Disease Ontology
DOID:0111057
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
28 ABO ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
821 CANX calnexin
2923 PDIA3 protein disulfide isomerase family A member 3
23545 ATP6V0A2 ATPase H+ transporting V0 subunit a2

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024