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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 11 - 20 of 72 in total
DO ID Disease Name Source
DOID:0110107 atrial heart septal defect 2
DOID:0110108 atrial heart septal defect 3
DOID:0110109 atrial heart septal defect 4
DOID:0110110 atrial heart septal defect 5
DOID:0110111 atrial heart septal defect 6
DOID:0110112 atrial heart septal defect 7
DOID:0110113 atrial heart septal defect 8
DOID:0110114 atrial heart septal defect 9
DOID:0110213 isolated cleft palate
DOID:0110892 inflammatory bowel disease 1
The Human Phenotype Ontology
Displaying entries 31 - 40 of 50 in total
HPO ID HPO Term
HP:0001903 Anemia
HP:0002092 Pulmonary arterial hypertension
HP:0002093 Respiratory insufficiency
HP:0002205 Recurrent respiratory infections
HP:0002240 Hepatomegaly
HP:0002619 Varicose veins
HP:0002718 Recurrent bacterial infections
HP:0002783 Recurrent lower respiratory tract infections
HP:0002788 Recurrent upper respiratory tract infections
HP:0003198 Myopathy
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 31 - 40 of 75 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
101097770 FELCA30949
122205957 PANLE04363
101327107 TURTR13454
118886111 BALMU10672
100657260 LOXAF10224
100512070 PIGXX02182
369023 BOVIN13473
102179979 CAPHI11011
105997519 DIPOR21858
100753219 CRIGR12827
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: August 19, 2024