| Description: | component of oligomeric golgi complex 2 [Source:HGNC Symbol;Acc:HGNC:6546] |
| Synonyms: | CDG2Q, LDLC |
| Other ID(s): | HGNC:6546, ENSG00000135775 |
| Protein Accession Numbers: | ENST00000366669.4, NP_001138508, ENST00000534989, ENST00000366669, ENST00000546013, ENST00000468893, ENST00000366668, NP_031383, ENST00000535166 |
| Statistics: | gnomAD(104) |
∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000366668
ENST00000366669
ENST00000468893
ENST00000534989
ENST00000535166
ENST00000546013
NP_001138508
NP_031383
| Pfam Domain filter_list | Domain Name filter_list | Description filter_list | Positions filter_list | Clan filter_list | Clan Name filter_list | Organism filter_list |
|---|---|---|---|---|---|---|
| NO RESULT FOUND | ||||||
| PF06148 | COG2 | COG (conserved oligomeric Golgi) complex component, COG2 | 15-147 | CL0295 | Vps51 | Mus musculus |
| PF12022 | DUF3510 | Domain of unknown function (DUF3510) | 565-692 | Mus musculus | ||
| Disease Name filter_list | Disease Category filter_list | DSI* filter_list | DPI** filter_list | ||
|---|---|---|---|---|---|
| Congenital Disorders of Glycosylation | Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Nutritional and Metabolic Diseases ; | 0.785 | 0.172 | ||
| CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq | N/A | 0.785 | 0.172 | ||
| NO RESULT FOUND | |||||