POMT2 Y666C

Stable Identifier
R-HSA-5617034
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Protein O-mannosyl-transferase 2 ecNumber2.4.1.109/ecNumber, POMT2_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
POMT2
Chain
chain:1-750
Reference Transcript
Other Identifiers
0005360040
00514+2.4.1.109
00515+2.4.1.109
11729527_a_at
11729528_a_at
16795082
220632_s_at
225560_at
29954
3572983
3572984
3572986
3572987
3572991
3572993
3572994
3572995
3572997
3572998
3572999
3573004
3573005
3573008
3573010
3573011
3573013
3573014
3573015
3573016
3573019
3573022
3573024
3573025
3663
47062_at
76739_at
76741_g_at
76743_at
7980358
A_24_P111134
AAF14118
AAF62558
AAF63184
AAH31651
AAM12046
AC007375
AC007954
AF105020
AL353956
AY090480
BC031651
BX248027
CAB89256
CAD62348
CCDS9857
ENSG00000009830
ENSP00000261534
ENSP00000450630
ENST00000261534
ENST00000556326
EntrezGene:29954
g7019494_3p_a_at
GE62413
GO:0000030
GO:0003674
GO:0004169
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005783
GO:0005789
GO:0005975
GO:0006464
GO:0006486
GO:0006493
GO:0006950
GO:0008150
GO:0009056
GO:0009058
GO:0016020
GO:0016021
GO:0016740
GO:0016757
GO:0035269
GO:0043167
GO:0043226
GO:0046872
GO:0071712
GO:0097502
GO:1904100
HGNC:19743
HPA003663
Hs.132989.1.S2_3p_at
ILMN_1678805
IPR003342
IPR016093
IPR027005
IPR032421
IPR036300
LRG_844
LRG_844t1
MIM:236670
MIM:607439
MIM:613150
MIM:613156
MIM:613158
NM_013382
NP_037514
PF02366
PF02815
PF16192
PH_hs_0007985
POMT2
POMT2-201
POMT2-214
SM00472
TC14001342.hg
uc001xti.3
uc059dtc.1
UPI0000070587
UPI00020F7A5E
XM_011536675
XM_011536676
XM_011536677
XM_011536679
XM_017021244
XM_017021245
XP_011534977
XP_011534978
XP_011534979
XP_011534981
XP_016876733
XP_016876734
XR_001750279
XR_001750282
XR_943416
Participant Of
Other forms of this molecule
Modified Residues
Name
L-tyrosine 666 replaced with L-cysteine
Coordinate
666
PsiMod HEY
A protein modification that effectively converts a source amino acid residue to an L-cysteine.
A protein modification that effectively removes or replaces an L-tyrosine.
Disease
Name Identifier Synonyms
muscular dystrophy-dystroglycanopathy 0050588
Cross References
RefSeq
GeneCards
PRO
BRENDA (Homo sapiens)
Orphanet
HMDB Protein