TPMT A167G

Stable Identifier
R-HSA-5603357
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Thiopurine S-methyltransferase, TPMT_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
TPMT
Chain
chain:1-245
Other Identifiers
0002350301
00983+2.1.1.67
11727822_a_at
11727823_x_at
11727824_at
11727825_x_at
17015975
19851
203671_at
203672_x_at
2944026
2944027
2944028
2944029
2944030
2944031
2944034
2944035
2944037
2944038
2944040
2944042
2944043
2944044
2944045
2BZG
2H11
32810_at
3787362
3787364
7172
8124134
A0A024QZW0
A_23_P214108
A_24_P397498
A_33_P3317321
AAB27277
AAB71625
AAB71626
AAB71627
AAB71628
AAB71629
AAB71630
AAB71631
AAB71632
AAB71633
AAB71634
AAB71635
AAB71636
AAB80746
AAB80747
AAC32289
AAC50130
AAC50368
AAC51865
AAH09596
AB045146
AF019364
AF019365
AF019366
AF019367
AF019368
AF019369
AF021876
AF021877
AF035426
AL589723
BAA97037
BC009596
CCDS4543
CH471087
EAW55396
EAW55397
ENSG00000137364
ENSP00000312304
ENST00000309983
EntrezGene:7172
g805083_3p_a_at
GE62974
GO:0003674
GO:0005575
GO:0005576
GO:0005615
GO:0005622
GO:0005623
GO:0005737
GO:0005829
GO:0006139
GO:0008119
GO:0008150
GO:0008168
GO:0008757
GO:0016740
GO:0032259
GO:0034641
GO:0043226
GO:0070062
HGNC:12014
HPA019851
Hs.296922.0.A4_3p_at
ILMN_1740185
ILMN_1760212
IPR008854
IPR025835
IPR029063
MIM:187680
MIM:610460
NM_000367
NP_000358
NP_001333746
PF05724
PH_hs_0024285
S62904
S62904_s_at
TC06001301.hg
TPMT
TPMT-201
U12387
U12387_s_at
U30512
U30513
U30514
U30515
U30516
U30517
U30518
U81562
U81563
U81564
U81565
U81566
U81567
U81568
U81569
U81570
U81571
U81572
U81573
uc003ncm.4
UPI0000137261
XM_011514839
XM_017011241
XP_016866730
Participant Of
Other forms of this molecule
Modified Residues
Name
L-alanine 167 replaced with glycine
Coordinate
167
PsiMod HEY
A protein modification that effectively removes or replaces an L-alanine.
A protein modification that effectively converts a source amino acid residue to a glycine.
Disease
Name Identifier Synonyms
inherited metabolic disorder 655 Metabolic hereditary disorder, Inborn Errors of Metabolism, inborn metabolism disorder
Cross References
ZINC - Substances
ZINC - Biogenic
ZINC target
PRO
PDB
ZINC - Metabolites
GeneCards
DOCK Blaster
BRENDA (Homo sapiens)
ZINC - Predictions - Purchasable
Orphanet
HMDB Protein