coronin-1A deficiency

Summary
Definition
A severe combined immunodeficiency that is an actin regulator when mutated results in SCID through inhibition of thymic egress of mature thymocytes into peripheral lymphoid organs.
Super Class
severe combined immunodeficiency
Disease Ontology
DOID:0060019
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
11151 CORO1A coronin 1A
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P31146 Coronin-1A

About Release Notes Help Feedback

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: [email protected]

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.5.0

Last updated: April 6, 2026