ALG14 P65L [endoplasmic reticulum membrane]

Stable Identifier
R-HSA-5633218
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
UDP-N-acetylglucosamine transferase subunit ALG14 homolog, ALG14_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
ALG14
Chain
chain:1-216
Other Identifiers
0004480021
11743909_at
1553954_at
16689923
199857
2424140
2424141
2424143
2424145
2424147
2424149
2424150
2424151
2424152
2424160
2424170
2424172
2424173
7917896
84301_at
84303_g_at
A_23_P257423
GE80389
GO:0005575
GO:0005622
GO:0005634
GO:0005635
GO:0005737
GO:0005783
GO:0005789
GO:0006464
GO:0006488
GO:0006629
GO:0008150
GO:0009058
GO:0016020
GO:0016021
GO:0031965
GO:0032991
GO:0043226
GO:0043541
Hs2.124005.1.S1_3p_at
ILMN_1743635
ILMN_2191822
PH_hs_0026538
TC01002892.hg
Participant Of
Other forms of this molecule
Modified Residues
Name
L-proline 65 replaced with L-leucine
Coordinate
65
PsiMod
A protein modification that effectively removes or replaces an L-proline.
A protein modification that effectively converts a source amino acid residue to an L-leucine.
Disease
Name Identifier Synonyms
congenital myasthenic syndrome 3635
Cross References
OpenTargets
GeneCards
PRO
Orphanet
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