Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
glucose-6-phosphatase catalytic subunit 3
Summary
- Gene Symbol
-
- G6PC3
- Aliases
-
- UGRP
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Disease variant
- Endoplasmic reticulum
- Gluconeogenesis
- Hydrolase
- Proteomics identification
- Reference proteome
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A8Q3SIG5 |
|
| Q9BUM1 |
|
| K7EJC5 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| glucose 6-phosphate metabolic process | ||
| glucose-6-phosphate transport | ||
| gluconeogenesis |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| membrane |
GO Hierarchy
GO Hierarchy
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0111040 | glycogen storage disease IXd | |
| DOID:0111041 | glycogen storage disease IXb | |
| DOID:0111042 | glycogen storage disease IXa | |
| DOID:0111043 | glycogen storage disease IXc | |
| DOID:0112136 | severe congenital neutropenia 4 | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:1059 | intellectual disability | |
| DOID:10787 | premature menopause | |
| DOID:10907 | microcephaly | |
| DOID:11111 | hydronephrosis |
- The Human Phenotype Ontology
| 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 |
| Disease ID | Disease Name |
|---|---|
| OMIM:612541 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 108532178 | RHIBE27898 | ||
| 104654704 | RHIRO29411 | ||
| 100584622 | NOMLE15945 | ||
| 114582372 | PODMU00363 | ||
| 107562003 | SINGR76089 | ||
| 106836447 | EQUAS09493 | ||
| 116831487 | CHEAB01446 | ||
| 115059848 | ECHNA46637 | ||
| 115393203 | SALFA41291 | ||
| 113490602 | ATHCN22563 |
