glycogen storage disease Ia

Summary
Definition
A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PC gene, which encodes glucose-6-phosphatase (G6Pase), on chromosome 17q21.
Super Class
autosomal recessive disease glycogen storage disease I
External Links
Disease Ontology
DOID:2749
Mondo Disease Ontology
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
2538 G6PC1 glucose-6-phosphatase catalytic subunit 1
2542 SLC37A4 solute carrier family 37 member 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
14377 G6pc1 glucose-6-phosphatase catalytic subunit 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
25634 G6pc1 glucose-6-phosphatase catalytic subunit 1
The Human Phenotype Ontology
Displaying entry 31 - 31 of 31 in total
HPO ID HPO Term
HP:0000991 Xanthomatosis
Displaying 1 entry
Gene ID Gene Symbol Description
2538 G6PC1 glucose-6-phosphatase catalytic subunit 1

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: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024