CYP26B1 R363L

Stable Identifier
R-HSA-5602041
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Cytochrome P450 26B1, C26A_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
CYP26B1, CYP26A2, P450RAI2
Chain
chain:1-512
Other Identifiers
0001660010
11730353_a_at
11730354_a_at
12567
16898911
219825_at
234721_s_at
2559190
2559191
2559192
2559193
2559194
2559195
2559196
2559205
2559216
55426_at
56603
8052947
A_23_P210100
A_23_P210109
AAF76003
AAH69443
AAI09206
AAY14690
AC007002
ACR19332
AF252297
AK294814
AK294933
AK295683
AK313433
BAG36224
BAH11892
BAH11930
BAH12154
BC069443
BC109205
CCDS1919
CCDS62934
CYP26B1
CYP26B1-201
CYP26B1-205
ENSG00000003137
ENSP00000001146
ENSP00000443304
ENST00000001146
ENST00000546307
EntrezGene:56603
FJ467289
g9845284_3p_at
GE61521
GO:0000003
GO:0001709
GO:0001768
GO:0001972
GO:0002376
GO:0003674
GO:0004497
GO:0005506
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005783
GO:0005789
GO:0006629
GO:0006766
GO:0006805
GO:0006950
GO:0006954
GO:0007049
GO:0007140
GO:0007155
GO:0007165
GO:0007283
GO:0008150
GO:0008219
GO:0008289
GO:0008401
GO:0009056
GO:0009790
GO:0009954
GO:0010628
GO:0016020
GO:0016125
GO:0016491
GO:0016705
GO:0016709
GO:0020037
GO:0030154
GO:0030326
GO:0031090
GO:0034653
GO:0042573
GO:0042592
GO:0043167
GO:0043226
GO:0043231
GO:0043587
GO:0044281
GO:0045580
GO:0046872
GO:0048384
GO:0048385
GO:0048387
GO:0048856
GO:0055114
GO:0060349
GO:0061436
GO:0070268
GO:0071300
GO:2001037
HGNC:20581
HPA012567
Hs.91546.1.S1_3p_a_at
ILMN_1812297
IPR001128
IPR002403
IPR017972
IPR036396
MIM:605207
MIM:614416
NM_001277742
NM_019885
NP_001264671
NP_063938
PF00067
PH_hs_0005084
PR00385
PR00465
TC02001976.hg
uc002sih.3
uc010yrb.2
UPI000003DC62
UPI0001914D61
XM_005264433
XP_005264490
Other forms of this molecule
Modified Residues
Name
L-arginine 363 replaced with L-leucine
Coordinate
363
PsiMod HEY
A protein modification that effectively removes or replaces an L-arginine.
A protein modification that effectively converts a source amino acid residue to an L-leucine.
Disease
Name Identifier Synonyms
craniosynostosis 2340 Premature closure of cranial sutures
Cross References
GeneCards
PRO
Orphanet
HMDB Protein