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
AAC95426
AAD20021
AAI36575
AAK11850
AF029403
AF127090
AF176800
AF176801
AF176802
AF176803
AF176804
AF176805
BC136574
CCDS6180
CH471068
CYP7B1
CYP7B1-201
EAW86877
ENSG00000172817
ENSP00000310721
ENST00000310193
EntrezGene:9420
g13787190_3p_at
GE58345
GO:0000003
GO:0002376
GO:0003674
GO:0004497
GO:0005506
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005783
GO:0005789
GO:0006629
GO:0006699
GO:0007165
GO:0008150
GO:0008202
GO:0008203
GO:0008283
GO:0008396
GO:0009058
GO:0016020
GO:0016125
GO:0016491
GO:0016705
GO:0020037
GO:0031090
GO:0033147
GO:0035754
GO:0040011
GO:0043167
GO:0043226
GO:0043231
GO:0044281
GO:0046872
GO:0048856
GO:0048870
GO:0050679
GO:0055114
GO:0060740
HGNC:2652
HPA017761
ILMN_1701661
IPR001128
IPR002403
IPR024204
IPR036396
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
GeneCards
PRO
BRENDA (Homo sapiens)
Orphanet
HMDB Protein