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CYP4F22 H435Y

Stable Identifier
R-HSA-5602287
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Cytochrome P450 4F22, CP4FN_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
CYP4F22
Chain
chain:1-531
Other Identifiers
11733532_at
11733533_at
126410
16859117
244692_at
58960
8026424
91481_at
AAH69351
AAH93894
AAH93896
BAC04868
CCDS12331
CYP4F22
CYP4F22-201
CYP4F22-202
ENSG00000171954
ENSP00000269703
ENSP00000469866
ENST00000269703
ENST00000601005
EntrezGene:126410
GE85609
GO:0004497
GO:0005506
GO:0005783
GO:0005789
GO:0006690
GO:0016020
GO:0016491
GO:0016705
GO:0020037
GO:0031090
GO:0043231
GO:0046872
GO:0055114
HGNC:26820
HPA058960
Hs.156452
Hs.156452.0.A1_3p_at
ILMN_1708303
MIM:611495
NM_173483
NP_775754
PF00067
PH_hs_0009443
PR00385
PR00463
TC19000272.hg
uc002nbh.5
uc060uuh.1
UPI000013D84B
XM_011527692
XM_011527693
XP_011525994
XP_011525995
Participant Of
Other forms of this molecule
Modified Residues
Name
L-histidine 435 replaced with L-tyrosine
Coordinate
435
PsiMod HEY
A protein modification that effectively removes or replaces an L-histidine.
A protein modification that effectively converts a source amino acid residue to L-tyrosine.
Disease
Name Identifier Synonyms
congenital ichthyosiform erythroderma 1699 lamellar ichthyosis, Ichthyosiform erythroderma, Alligator skin, nonbullous congenital ichthyosiform erythroderma, Congenital non bullous ichthyosiform erythroderma
Cross References
GeneCards
PRO
Orphanet
HMDB Protein