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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 11 - 20 of 50 in total
HPO ID HPO Term
HP:0000388 Otitis media
HP:0000407 Sensorineural hearing impairment
HP:0000431 Wide nasal bridge
HP:0000768 Pectus carinatum
HP:0000778 Hypoplasia of the thymus
HP:0000954 Single transverse palmar crease
HP:0001015 Prominent superficial veins
HP:0001263 Global developmental delay
HP:0001433 Hepatosplenomegaly
HP:0001508 Failure to thrive
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 51 - 60 of 75 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
101061994 TAKRU25049
110215726 PHACI19261
101036723 SAIBB38456
101971812 ICTTR02923
101617406 JACJA06741
118287317 SCOMX12908
102425980 MYOLU06955
117012927 RHIFE07937
115490648 TAEGU15494
103243337 CHLSB05825
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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