FMO3 N61S [endoplasmic reticulum membrane]

Stable Identifier
R-HSA-5602964
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Dimethylaniline monooxygenase (N-oxide forming) 3, Hepatic flavin-containing monooxygenase 3, Dimethylaniline oxidase 3, FMO form 2, FMO II
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
FMO3
Chain
initiator methionine:1, chain:2-532
Other Identifiers
0003290673
11726051_a_at
16673682
206496_3p_at
206496_at
2328
2366942
2366943
2366944
2366948
2366949
2366950
2366951
2366954
2366955
2366958
2366961
2366962
2366964
2366965
2366966
2366967
40665_3p_at
40665_at
4859786_3p_at
7907249
A_23_P155596
A_23_P155601
GE58109
GO:0003674
GO:0004497
GO:0004499
GO:0005515
GO:0005575
GO:0005622
GO:0005737
GO:0005783
GO:0005789
GO:0006805
GO:0008150
GO:0016020
GO:0016021
GO:0016491
GO:0031090
GO:0034899
GO:0043167
GO:0043226
GO:0043231
GO:0050660
GO:0050661
GO:0055114
ILMN_1808657
ILMN_2344283
M83772_at
PH_hs_0031359
TC01001486.hg
g6325466_3p_at
g6325466_3p_s_at
Participant Of
Other forms of this molecule
Modified Residues
Name
L-asparagine 61 replaced with L-serine
Coordinate
61
PsiMod
A protein modification that effectively removes or replaces an L-asparagine.
A protein modification that effectively converts a source amino acid residue to L-serine.
Disease
Name Identifier Synonyms
inherited metabolic disorder 655 Metabolic hereditary disorder, Inborn Errors of Metabolism, inborn metabolism disorder
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