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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 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 1 - 10 of 75 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
33476 FB:FBgn0031463
103183778 CALMI28310
790919 ZFIN:ZDB-GENE-061215-19 DANRE04727
103023782 ASTMX20192
100528077 ICTPU05509
113574294 ELEEL15488
106589637 SALSA99326
115201452 SALTR100457
115530905 GADMO23110
101162637 ORYLA08194
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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