MECP2_e2 R133C [nucleoplasm]

Stable Identifier
R-HSA-9022488
Type
Genes and Transcripts [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
MECP2A R133C
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
MECP2
Other Identifiers
0006510725
11722682_at
11722683_a_at
11722684_a_at
1341
17115453
1QK9
202616_s_at
202617_s_at
202618_s_at
34355_at
37264
3C2I
4027057
4027058
4027059
4027060
4027061
4027062
4027080
4027081
4027090
4027091
4027092
4204
593
5BT2
6C1Y
8175998
A0A087WVW7
A0A087X1U4
A0A0D9SEX1
A0A0D9SFX7
A0A140VKC4
A_23_P114361
A_24_P237486
A_33_P3317211
A_33_P3339036
AAC08757
AAC32737
AAF33023
AAH11612
AAS55455
ADD17354
ADK25711
AEE61261
AF030876
AF158180
AJ132917
ALQ33632
AY541280
B5MCB4
BC011612
BX538060
C9JH89
CAA61599
CAA64331
CAA68001
CAA73190
CAB037264
CAB46446
CAD97991
CCDS14741
CCDS48193
CH471172
D3YJ43
EAW72757
EAW72759
ENSG00000169057
ENSP00000301948
ENSP00000395535
ENST00000303391
ENST00000303391.10
ENST00000453960
ENST00000453960.6
EntrezGene:4204
g7710148_3p_a_at
g972764_3p_a_at
GE54240
GO:0000122
GO:0000785
GO:0000792
GO:0001227
GO:0001662
GO:0001666
GO:0001964
GO:0001976
GO:0002087
GO:0003674
GO:0003677
GO:0003700
GO:0003714
GO:0003723
GO:0003729
GO:0005515
GO:0005575
GO:0005615
GO:0005634
GO:0005654
GO:0005737
GO:0005739
GO:0005813
GO:0005815
GO:0005829
GO:0005975
GO:0006020
GO:0006091
GO:0006122
GO:0006342
GO:0006349
GO:0006355
GO:0006367
GO:0006464
GO:0006520
GO:0006541
GO:0006576
GO:0006629
GO:0006810
GO:0006950
GO:0007010
GO:0007052
GO:0007267
GO:0007268
GO:0007416
GO:0007420
GO:0007585
GO:0007612
GO:0007613
GO:0007616
GO:0008104
GO:0008134
GO:0008150
GO:0008211
GO:0008284
GO:0008327
GO:0008344
GO:0008542
GO:0009058
GO:0009314
GO:0009405
GO:0009791
GO:0010385
GO:0010468
GO:0010629
GO:0010971
GO:0016358
GO:0016525
GO:0016571
GO:0016573
GO:0019230
GO:0019233
GO:0019904
GO:0021549
GO:0021591
GO:0021700
GO:0022607
GO:0030154
GO:0030182
GO:0031061
GO:0031175
GO:0032048
GO:0033555
GO:0034641
GO:0035067
GO:0035176
GO:0035197
GO:0040029
GO:0042551
GO:0043226
GO:0043524
GO:0043537
GO:0044281
GO:0045892
GO:0045893
GO:0046470
GO:0047485
GO:0048167
GO:0048856
GO:0050432
GO:0050877
GO:0050884
GO:0050905
GO:0051151
GO:0051965
GO:0060079
GO:0060291
GO:0090063
GO:0098794
GO:1900114
GO:1905643
GO:2000820
GU479943
H7BY72
HGNC:6990
HM005664
HM156733
HPA000593
HPA001341
Hs.3239.0.S2_3p_a_at
I6LM39
ILMN_1682091
ILMN_1702715
IPR001739
IPR016177
IPR017353
KU178174
L37298
MECP2
MECP2-201
MECP2-205
MIM:300005
MIM:300055
MIM:300260
MIM:300496
MIM:300673
MIM:312750
NM_001110792
NM_001316337
NM_004992
NP_001104262
NP_001303266
NP_004983
PF01429
PH_hs_0000399
SM00391
UPI000012EEA5
UPI0000253F1B
X89430
X89430_at
X94628
X94628_rna1_s_at
X99686
XM_006724819
XM_011531166
XM_024452383
XM_024452384
XP_006724882
XP_011529468
XP_024308151
XP_024308152
Y12643
Participant Of
Other forms of this molecule
Modified Residues
Name
L-arginine 133 replaced with L-cysteine
Coordinate
133
PsiMod
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-arginine.
Disease
Name Identifier Synonyms
Rett syndrome 1206 Rett's disorder, cerebroatrophic hyperammonemia
Cross References
OpenTargets
GeneCards
PRO
Orphanet
PDB