| Type | Description |
|---|---|
| Definition | mannosyl-oligosaccharide glucosidase |
| Date | Results | Publications |
|---|---|---|
| 2019-04-13 12:19:00 | Compound heterozygous variants in MOGS gene is associated with congenital disorders of glycosylation IIb. | 30587846 |
| 2014-06-14 11:59:00 | A shortened immunoglobulin half-life was determined to be the mechanism underlying the hypogammaglobulinemia in congenital disorder of glycosylation type IIb (CDG-IIb). | 24716661 |
| 2010-01-21 00:00:00 | MafF/NFE2 hetrodimers act as weak transcriptional activators, and, in particular, are able to stimulate activity of the GCS1 promoter. | 12490281 |
| 2010-01-21 00:00:00 | identification of sequence motifs responsible for endoplasmic reticulum localization | 12626409 |
| 2010-01-21 00:00:00 | Perturbation of free oligosaccharide trafficking in endoplasmic reticulum glucosidase I-deficient and castanospermine-treated cells. | 11942856 |
| Type | IDs |
|---|---|
| Synonymous | CDG2B, CWH41, DER7, GCS1 |
| Gene |
UniProtKB-ID:
MOGS_HUMAN,
A0A384MDR6_HUMAN,
Q58F09_HUMAN
UniprotKB:
Q13724,
A0A384MDR6,
Q58F09
UniParc:
UPI00004F6ECC,
UPI000006FEFF,
UPI000198D4B5
EMBL:
CH471053,
BC117252,
AK292553,
X87237,
GQ891420,
AC005041,
BC117250,
AJ422288,
BC028337
Ensembl:
ENSG00000115275
KO:
hsa:7841
|
| Nucleutide sequences |
EMBL-CDS:
CAD19636.1,
AAI17251.1,
CAA60683.1,
EAW99653.1,
BAF85242.1,
AAI17253.1,
ADO22282.1,
AAH28337.1
Ensembl_TRS:
ENST00000448666,
ENST00000452063
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000410992,
ENSP00000388201
RefSeq:
NP_006293.2,
NP_001139630.1
|
| Others |
UniRef100:
UniRef100_Q58F09,
UniRef100_Q13724
UniRef90:
UniRef90_Q13724
UniRef50:
UniRef50_Q13724
UniGene:
Hs.516119
CCDS:
CCDS42700.1,
CCDS54370.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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