Gene Symbol:
GYS1
HGNC:4706
Locus Group:
protein-coding gene
Locus Type:
gene with protein product
Location:
19q13.33
Filters:

ClinGen classifications

glycogen storage disease due to muscle and heart glycogen synthase deficiency
AR
02/12/2024
Evaluated
04/21/2024
Submitted

Genomics England PanelApp classifications

glycogen storage disease due to muscle and heart glycogen synthase deficiency
Submitted as: OMIM:611556
AR
06/23/2020
Evaluated
03/31/2021
Submitted

Invitae classifications

glycogen storage disease due to muscle and heart glycogen synthase deficiency
Submitted as: OMIM:611556
AR
12/15/2018
Evaluated
11/30/2023
Submitted

Orphanet classifications

glycogen storage disease due to muscle and heart glycogen synthase deficiency
Submitted as: Orphanet:137625
AR
09/14/2021
Evaluated
09/14/2021
Submitted

PanelApp Australia classifications

glycogen storage disease due to muscle and heart glycogen synthase deficiency
Submitted as: OMIM:611556
AR
03/06/2021
Evaluated
03/09/2021
Submitted

The GenCC data are available free of restriction under a CC0 1.0 Universal (CC0 1.0) Public Domain Dedication. The GenCC requests that you give attribution to GenCC and the contributing sources whenever possible and appropriate. The accepted Flagship manuscript is now available from Genetics in Medicine (https://www.gimjournal.org/article/S1098-3600(22)00746-8/fulltext).

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. The GenCC does not independently verify the submitted information. Though the information is obtained from sources believed to be reliable, no warranty, expressed or implied, is made regarding accuracy, adequacy, completeness, reliability or usefulness of any information. This disclaimer applies to both isolated and aggregate uses of the information. The information is provided on an "as is" basis, collected through periodic submission and therefore may not represent the most up-to-date information from the submitters. If you have questions about the medical relevance of information contained on this website, please see a healthcare professional; if you have questions about specific gene-disease claims, please contact the relevant sources; and if you have questions about the representation of the data on this website, please contact gencc@thegencc.org.