CYP11B1 T318M [mitochondrial inner membrane]

Stable Identifier
R-HSA-5580293
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
mitochondrial inner membrane
Synonyms
Cytochrome P450 11B1, CPN1_HUMAN
Locations in the PathwayBrowser
Expand all
External Reference Information
External Reference
UniProt:P15538 CYP11B1
Gene Names
CYP11B1, S11BH
Chain
transit peptide:1-24, chain:25-503
Reference Genes
BioGPS Gene:1584 CYP11B1
COSMIC (genes):CYP11B1 CYP11B1
CTD Gene:1584 CYP11B1
dbSNP Gene:1584 CYP11B1
ENSEMBL:ENSG00000160882 CYP11B1
HGNC:2591 CYP11B1
Monarch:1584 CYP11B1
NCBI Gene:1584 CYP11B1
OMIM:610613 CYP11B1
UCSC:P15538 CYP11B1
Reference Transcript
Other Identifiers
11734127_a_at
11734128_a_at
1412_g_at
1552493_PM_s_at
1552493_s_at
1584
17081986
214610_PM_at
214610_at
3157216
3157218
3157219
3157220
3157221
3157222
3157223
3157225
3157226
3157227
3157228
3157229
3157230
3157231
3157232
3157233
3157234
3157235
3157236
3157237
3157238
3157239
3157240
3157247
3157249
3157250
3157251
3157252
3157255
3157257
34548_at
34549_g_at
79018_at
8153363
A_23_P168928
A_24_P329424
GE59810
GO:0002376
GO:0003824
GO:0004497
GO:0004507
GO:0005506
GO:0005739
GO:0005743
GO:0005789
GO:0006629
GO:0006694
GO:0006700
GO:0006704
GO:0006955
GO:0008203
GO:0008217
GO:0016125
GO:0016491
GO:0016705
GO:0020037
GO:0032342
GO:0032870
GO:0034650
GO:0034651
GO:0035865
GO:0042593
GO:0043226
GO:0046872
GO:0047783
GO:0071375
GO:1901615
HMNXSV003012949
HMNXSV003041760
Hs.301118.0.S2_3p_at
Hs2.377912.1.S1_3p_s_at
ILMN_1801917
ILMN_2358436
M32879_at
M32879_s_at
PH_hs_0035658
TC08001708.hg
Participates
as a member of
Other forms of this molecule
CYP11B1 R448H [mitochondrial inner membrane]
CYP11B1 R374Q [mitochondrial inner membrane]
CYP11B1 A331V [mitochondrial inner membrane]
CYP11B1 E371G [mitochondrial inner membrane]
CYP11B1 R448C [mitochondrial inner membrane]
CYP11B1 [mitochondrial inner membrane]
Modified Residues
Name
L-threonine 318 replaced with L-methionine
Coordinate
318
PsiMod
L-methionine residue [MOD:00022]
A protein modification that effectively converts a source amino acid residue to L-methionine.
L-threonine removal [MOD:01647]
A protein modification that effectively removes or replaces an L-threonine.
Disease
Name Identifier Synonyms
adrenal gland disease DOID:9553
Cross References
ZINC - World Drugs
Guide to Pharmacology - Targets
ENSEMBL
OpenTargets
ZINC - FDA approved
ZINC - Substances
ZINC target
PRO
PDB
ZINC - Investigational
HPA
Pharos - Targets
Orphanet
ZINC - Predictions - Purchasable
HMDB Protein
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