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CYP7B1 S363F

Stable Identifier
R-HSA-5603011
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Cytochrome P450 7B1, CP7B_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
CYP7B1
Chain
chain:1-506
Reference Transcript
Other Identifiers
0002480100
11740151_at
17077723
17761
207386_at
3138207
3138208
3138209
3138211
3138218
3138219
3138220
3138221
3138223
3138246
3138247
3138248
33055_at
8151056
9420
CCDS6180
CYP7B1
CYP7B1-201
ENSG00000172817
ENSP00000310721
ENST00000310193
EntrezGene:9420
g13787190_3p_at
GE58345
GO:0004497
GO:0005506
GO:0005783
GO:0005789
GO:0006629
GO:0006699
GO:0008202
GO:0008203
GO:0008396
GO:0016020
GO:0016125
GO:0016491
GO:0016705
GO:0020037
GO:0031090
GO:0033147
GO:0035754
GO:0043231
GO:0046872
GO:0050679
GO:0055114
GO:0060740
HGNC:2652
HPA017761
Hs.667720
ILMN_1701661
MIM:270800
MIM:603711
MIM:613812
NM_004820
NP_004811
PF00067
PH_hs_0008586
PR00385
PR00465
TC08001275.hg
uc003xvj.3
UPI0000128218
XM_017014002
XP_016869491
Participant Of
Other forms of this molecule
Modified Residues
Name
L-serine 363 replaced with L-phenylalanine
Coordinate
363
PsiMod HEY
A protein modification that effectively removes or replaces an L-serine.
A protein modification that effectively converts a source amino acid residue to L-phenylalanine.
Disease
Name Identifier Synonyms
hereditary spastic paraplegia 2476 Hereditary spastic paraplegia, Hereditary spastic paraplegia, Hereditary spastic paraplegia (disorder), Hereditary spastic paraplegia, familial spastic paraplegia, HSMN V
Cross References
RefSeq
Brenda
GeneCards
PRO
Orphanet
HMDB Protein