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Repository for lectin-assisted multimodality data
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MIRAGE
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 |
|---|---|---|
| gluconeogenesis | ||
| gluconeogenesis | ||
| gluconeogenesis | ||
| glucose-6-phosphate transport | ||
| glucose 6-phosphate metabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| membrane | ||
| membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| glucose-6-phosphatase activity | ||
| glucose-6-phosphatase activity | ||
| glucose-6-phosphatase activity | ||
| glucose-6-phosphatase activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Glucose-6-phosphatase
- Functional Category
-
- E: Amino acid transport and metabolism
- J: Translation, ribosomal structure and biogenesis
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| gluconeogenesis |
| glucose-6-phosphatase activity |
| hydrolase activity |
| InterPro |
|---|
| Glucose-6-phosphatase |
| Phosphatidic acid phosphatase type 2/haloperoxidase superfamily |
| Phosphatidic acid phosphatase type 2/haloperoxidase |
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0112136 | severe congenital neutropenia 4 |
- The Human Phenotype Ontology
| 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 |
| Disease ID | Disease Name |
|---|---|
| OMIM:612541 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 2538 | FB:FBgn0031463 | ||
| 14377 | FB:FBgn0031463 | ||
| 14378 | FB:FBgn0031463 | ||
| 25634 | FB:FBgn0031463 | ||
| 57818 | FB:FBgn0031463 | ||
| 68401 | ZFIN:ZDB-GENE-061215-19 | MOUSE04898 | |
| 92579 | Xenbase:XB-GENE-6486406 | ||
| 303565 | ZFIN:ZDB-GENE-061215-19 | RATNO01001 | |
| 369023 | BOVIN13473 | ||
| 454720 | PANTR13758 |
