| Type | Description |
|---|---|
| Definition | ALG2 alpha-1,3/1,6-mannosyltransferase |
| Date | Results | Publications |
|---|---|---|
| 2013-04-27 12:09:00 | We identify ALG14 and ALG2 as novel genes in which mutations cause a congenital myasthenic syndrome | 23404334 |
| 2010-01-21 00:00:00 | The ALG2 binding site is necessary for the punctate distribution of the carboxyl-terminal proline-rich region of Alix in HeLa cells. | 14999017 |
| 2010-01-21 00:00:00 | The expression and transport of ALG-2 in association with TSG101 and Vps4B are reported. | 16004603 |
| Type | IDs |
|---|---|
| Synonymous | CDG1I, CDGIi, CMS14, CMSTA3, NET38, hALPG2 |
| Gene |
UniProtKB-ID:
ALG2_HUMAN,
A0A024R184_HUMAN
UniprotKB:
Q9H553,
A0A024R184
UniParc:
UPI0000073E01,
UPI0000039E65
EMBL:
AK074704,
AK027417,
CH471105,
AK074988,
AY358697,
AL137067,
AB161356,
BC017876,
AK075172
Ensembl:
ENSG00000119523
KO:
hsa:85365
|
| Nucleutide sequences |
EMBL-CDS:
AAQ89060.1,
BAD11905.1,
BAB55099.1,
BAC11337.1,
BAC11449.1,
BAC11150.1,
AAH17876.1,
EAW58908.1,
EAW58909.1
Gene_ORFName:
UNQ666/PRO1298,
hCG_30158
Ensembl_TRS:
ENST00000476832,
ENST00000319033
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000326609,
ENSP00000417764
RefSeq:
NP_149078.1
|
| Others |
UniRef100:
UniRef100_Q9H553
UniRef90:
UniRef90_Q9H553
UniRef50:
UniRef50_Q9H553
UniGene:
Hs.40919
CCDS:
CCDS6739.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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