CYP7B1 G57R

Stable Identifier
R-HSA-5602867
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
glycine 57 replaced with L-arginine
Coordinate
57
PsiMod HEY
A protein modification that effectively converts a source amino acid residue to an L-arginine.
A protein modification that effectively removes or replaces an glycine.
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