PGM1 T115A [cytosol]

Stable Identifier
R-HSA-5609931
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
phosphoglucomutase 1, Phosphoglucomutase , Glucose phosphomutase
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
PGM1
Chain
chain:1-562
Other Identifiers
0006770019
11748423_a_at
11756127_a_at
16665566
201968_s_at
2339787
2339788
2339789
2339794
2339795
2339796
2339799
2339800
2339802
2339804
2339806
2339807
2339808
2339811
2339814
2339819
2339827
2339828
2339829
2339830
2339832
32210_at
5236
7901951
A_14_P108033
A_23_P52031
GE58103
GO:0000287
GO:0002376
GO:0003674
GO:0004614
GO:0005515
GO:0005575
GO:0005576
GO:0005615
GO:0005622
GO:0005737
GO:0005829
GO:0005975
GO:0005978
GO:0005980
GO:0006006
GO:0006091
GO:0006094
GO:0006096
GO:0006810
GO:0008150
GO:0009056
GO:0009058
GO:0016192
GO:0016853
GO:0016868
GO:0019388
GO:0031410
GO:0034641
GO:0043167
GO:0043226
GO:0043312
GO:0044281
GO:0046872
GO:0070062
GO:0071704
GO:1904724
GO:1904813
ILMN_1800659
M83088_at
PH_hs_0000249
TC01000722.hg
g4505764_3p_a_at
Participant Of
Other forms of this molecule
Modified Residues
Name
L-threonine 115 replaced with L-alanine
Coordinate
115
PsiMod
A protein modification that effectively removes or replaces an L-threonine.
A protein modification that effectively converts a source amino acid residue to an L-alanine.
Disease
Name Identifier Synonyms
congenital disorder of glycosylation 5212 carbohydrate-deficient glycoprotein syndrome
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