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
00520+5.4.2.10
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
2339832
24190
24637
32210_at
46329
4666
5236
5EPC
5F9C
5HSH
5JN5
5TR2
7901951
A_14_P108033
A_23_P52031
AAA60080
AAB29177
AAB29178
AAH01756
AAH19920
AAH67763
AAH90856
AAP35607
BAG35186
BAG60712
CAB004666
CCDS53323
CCDS53324
CCDS625
ENSG00000079739
ENSP00000360124
ENSP00000360125
ENSP00000443449
ENST00000371083
ENST00000371084
ENST00000540265
EntrezGene:5236
g4505764_3p_a_at
GE58103
GO:0000287
GO:0002376
GO:0003674
GO:0004614
GO:0005515
GO:0005575
GO:0005576
GO:0005615
GO:0005622
GO:0005623
GO:0005737
GO:0005829
GO:0005856
GO:0005975
GO:0005978
GO:0005980
GO:0006006
GO:0006091
GO:0006094
GO:0006096
GO:0006810
GO:0008150
GO:0009056
GO:0009058
GO:0015629
GO:0016192
GO:0016853
GO:0016868
GO:0019388
GO:0031410
GO:0034641
GO:0034655
GO:0043167
GO:0043226
GO:0043312
GO:0044281
GO:0046872
GO:0051186
GO:0070062
GO:0071704
GO:1904724
GO:1904813
HGNC:8905
HPA024190
HPA024637
HPA046329
ILMN_1800659
IPR005841
IPR005843
IPR005844
IPR005845
IPR005846
IPR016055
IPR016066
IPR036900
M83088_at
MIM:171900
MIM:614921
NM_001172818
NM_001172819
NM_002633
NP_001166289
NP_001166290
NP_002624
PF00408
PF02878
PF02879
PF02880
PGM1
PGM1-201
PGM1-202
PGM1-205
PH_hs_0000249
PR00509
TC01000722.hg
uc001dbh.5
uc010ooy.4
uc010ooz.4
UPI000000105F
UPI000016A812
UPI00017A7786
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
Cross References
OpenTargets
GeneCards
DOCK Blaster
PRO
BRENDA (Homo sapiens)
Orphanet
HMDB Protein