| Type | Description |
|---|---|
| Definition | glucose-6-phosphatase, catalytic |
| Date | Results | Publications |
|---|---|---|
| 2019-01-05 11:46:00 | The results reveal a previously unrecognized physiological function of NFYA in controlling glucose metabolism by up-regulating the gluconeogenic genes Pck1 and G6pc. | 29530977 |
| 2018-11-10 10:09:00 | Hepatic mitochondrial dysfunction is a feature of glycogen storage disease type Ia with glucose-6-phosphatase deficiency. | 28317891 |
| 2018-04-14 11:55:00 | hepatic G6Pase-alpha deficiency causes metabolic reprogramming, leading to enhanced glycolysis and elevated hexose monophosphate shunt that along with impaired autophagy can contribute to hepatocellular adenoma/carcinoma development in glycogen storage disease type Ia. | 29545180 |
| 2017-08-19 12:30:00 | We envisage these data and models finding utility when investigating the muscle-specific functions of the 11beta-HSD1/G6PT/H6PDH triad. | 28749080 |
| 2017-06-24 12:57:00 | Data show that glucose-6-phosphatase and perilipin-5 (G6PC/PLIN5) are upregulated in notch1 knockout (KO) mice. | 27428080 |
| Type | IDs |
|---|---|
| Synonymous | AW107337, G6Pase, G6pt, Glc-6-Pase |
| Gene |
UniProtKB-ID:
G6PC_MOUSE
UniprotKB:
P35576
UniParc:
UPI00000216BC
EMBL:
U91573,
AK052656,
AK050279,
BC013448,
U00445,
AL590969
Ensembl:
ENSMUSG00000078650
KO:
mmu:14377
|
| Nucleutide sequences |
EMBL-CDS:
BAC35084.1,
AAC53166.1,
BAC34162.1,
AAH13448.1,
AAC52122.1
Ensembl_TRS:
ENSMUST00000019469
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000019469
RefSeq:
NP_032087.2
|
| Others |
UniRef100:
UniRef100_P35576
UniRef90:
UniRef90_P35576
UniRef50:
UniRef50_P35575
UniGene:
Mm.18064
CCDS:
CCDS25466.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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