CYP21A2 V237E

Stable Identifier
R-HSA-5601986
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Cytochrome P450 XXIB, CPS1_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
CYP21A2, CYP21, CYP21B
Chain
chain:1-494
Other Identifiers
0005570528
11729997_a_at
11738994_a_at
1589
17007178
17028240
17031103
17035809
17038330
17041090
214622_at
247_s_at
2903035
2903036
2903037
2903038
2903040
2903042
2903043
2903044
2903045
2903047
2903049
2903051
2903052
2903053
2903054
2903055
2903056
2GEG
4Y8W
53371
8118452
8118498
8178177
8179440
A_14_P138696
A_23_P257478
A_33_P3411279
AAA52064
AAA59695
AAA59706
AAA59985
AAA83248
AAB59440
AAI25183
ACT35412
ACT35422
ACT35427
AFK10105
AFK10106
AFK10107
AFK10108
AFK10111
AFK10112
AFK10113
AFK10136
AFK10137
AFK10140
AIG95650
AK054616
AL645922
AL662828
AL662849
AL844853
AL929593
BAB70774
BC125182
BX679671
CAA41709
CAM26070
CAQ07659
CCDS47406
CH471081
CR753845
CR936924
CYP21A2
CYP21A2-201
CYP21A2-211
CYP21A2-222
CYP21A2-238
CYP21A2-248
CYP21A2-258
EAX03570
ENSG00000198457
ENSG00000206338
ENSG00000231852
ENSG00000232414
ENSG00000233151
ENSG00000235134
ENSP00000372811
ENSP00000392321
ENSP00000398594
ENSP00000403230
ENSP00000403721
ENSP00000415043
ENST00000383321
ENST00000434026
ENST00000435122
ENST00000436607
ENST00000448314
ENST00000452386
EntrezGene:1589
GE61457
GO:0003674
GO:0004497
GO:0004509
GO:0005496
GO:0005506
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005783
GO:0005789
GO:0006629
GO:0006694
GO:0006704
GO:0006705
GO:0008150
GO:0008202
GO:0008289
GO:0008395
GO:0009058
GO:0016020
GO:0016125
GO:0016491
GO:0016705
GO:0020037
GO:0031090
GO:0043167
GO:0043226
GO:0043231
GO:0046872
GO:0055114
GQ222286
GQ222296
GQ222301
HGNC:2600
HPA048979
HPA053371
Hs.278430.0.S2_3p_at
ILMN_1773082
IPR001128
IPR002401
IPR017972
IPR036396
JF412030
JN034382
JN034383
JN034384
JN034385
JN034388
JN034389
JN034390
JQ993310
JQ993311
JQ993314
K02771
K9LHU1
M12792
M13936
M17252
M17252_at
M19711
M26856
M26856_s_at
MIM:201910
MIM:613815
NM_000500
NM_001128590
NP_000491
PF00067
PH_hs_0029576
PR00385
PR00463
Q16874
TC06000391.hg
TC06000393.hg
TC06002721.hg
TC6_cox_hap2000085.hg
TC6_dbb_hap3000076.hg
TC6_dbb_hap3000079.hg
TC6_mcf_hap5000069.hg
TC6_mcf_hap5000071.hg
TC6_qbl_hap6000072.hg
TC6_ssto_hap7000069.hg
uc003nzf.3
UPI000011D64D
UPI000013EB72
X58906
Participant Of
Other forms of this molecule
Modified Residues
Name
L-valine 237 replaced with L-glutamic acid
Coordinate
237
PsiMod HEY
A protein modification that effectively converts a source amino acid residue to an L-glutamic acid.
A protein modification that effectively removes or replaces an L-valine.
Disease
Name Identifier Synonyms
adrenal gland disease 9553
Cross References
ZINC - World Drugs
ZINC - FDA approved
GeneCards
ZINC - Substances
DOCK Blaster
ZINC target
PRO
BRENDA (Homo sapiens)
Orphanet
HMDB Protein
PDB