Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
glucose-6-phosphatase catalytic subunit 3

Summary
Gene Symbol
  • G6PC3
Aliases
  • UGRP
Organism
Homo sapiens (human)
External Links
NCBI Gene
92579
HGNC
24861
KEGG Gene ID
hsa:92579
PubChem
92579
Alliance of Genome Resources
Annotation
Keyword
  • Disease variant
  • Endoplasmic reticulum
  • Gluconeogenesis
  • Hydrolase
  • Proteomics identification
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying all 3 entries
UniProt Protein Name
A0A8Q3SIG5
Q9BUM1
  • Glucose-6-phosphatase beta
  • Ubiquitous glucose-6-phosphatase catalytic subunit-related protein
K7EJC5
Annotation information from UniProt.
Gene Ontology (GO)
Displaying all 3 entries
GO Term Evidence Code PMID
glucose 6-phosphate metabolic process
glucose-6-phosphate transport
gluconeogenesis
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
KEGG BRITE Database
Orthology
K01084
Name
glucose-6-phosphatase [EC:3.1.3.9]
References
Rhea

RHEA:16689

H2O + D-glucose 6-phosphate
D-glucose + phosphate
Enzyme
PMID

RHEA:44904

H2O + α-D-glucose 6-phosphate
α-D-glucose + phosphate
Enzyme
Disease
Disease Ontology
Displaying entries 61 - 70 of 72 in total
DO ID Disease Name Source
DOID:674 cleft palate
DOID:758 situs inversus
DOID:799 varicose veins
DOID:8577 ulcerative colitis
DOID:8778 Crohn's disease
DOID:8927 learning disability
DOID:9119 acute myeloid leukemia
DOID:9169 Wiskott-Aldrich syndrome
DOID:9266 cystinuria
DOID:9563 bronchiectasis
The Human Phenotype Ontology
Displaying entries 1 - 10 of 50 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000010 Recurrent urinary tract infections
HP:0000023 Inguinal hernia
HP:0000028 Cryptorchidism
HP:0000126 Hydronephrosis
HP:0000155 Oral ulcer
HP:0000175 Cleft palate
HP:0000218 High palate
HP:0000252 Microcephaly
HP:0000365 Hearing impairment
Displaying 1 entry
Disease ID Disease Name
OMIM:612541
  • autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
PubChem Disease
MedGen Diseases
OMIM Phenotypes
KEGG Diseases
Gene-Disease-Co-Occurrences-in-Literature (PubChem)
Ortholog
Displaying entries 41 - 50 of 75 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
68401 MGI:1915651 MOUSE04898
303565 RGD:727875 RATNO01001
100723248 CAVPO19039
101723886 HETGA22870
100022847 MONDO10860
100556520 ANOCA08648
114050832 VOMUR12340
113877224 BOBOX13680
105883539 MICMU06683
100941852 OTOGA14949
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