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MAOA Q296* [mitochondrial outer membrane]
Stable Identifier
R-HSA-5603089
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
mitochondrial outer membrane
Synonyms
MAO-A
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Metabolic disorders of biological oxidation enzymes (Homo sapiens)
Defective MAOA causes Brunner syndrome (BRUNS) (Homo sapiens)
Defective MAOA does not oxidatively deaminate 5HT (Homo sapiens)
MAOA Q296*:FAD [mitochondrial outer membrane] (Homo sapiens)
MAOA Q296* [mitochondrial outer membrane] (Homo sapiens)
External Reference Information
External Reference
UniProt:P21397 MAOA
Gene Names
MAOA
Chain
chain:1-527
Reference Genes
BioGPS Gene:4128 MAOA
COSMIC (genes):MAOA MAOA
CTD Gene:4128 MAOA
dbSNP Gene:4128 MAOA
ENSEMBL:ENSG00000189221 MAOA
HGNC:6833 MAOA
KEGG Gene (Homo sapiens):4128 MAOA
Monarch:4128 MAOA
NCBI Gene:4128 MAOA
OMIM:309850 MAOA
UCSC:P21397 MAOA
Reference Transcript
RefSeq:NM_001270458.1 MAOA
RefSeq:NM_000240.3 MAOA
Other Identifiers
0002970494
11719676_s_at
11745922_a_at
11745923_x_at
11755443_a_at
17102829
204388_s_at
204389_at
212741_at
3975228
3975229
3975230
3975231
3975232
3975233
3975238
3975242
3975248
3975250
3975251
3975252
3975253
3975254
3975256
3975257
3975258
3975259
3975260
4055670
4055674
4055678
4055680
4055682
4055684
4055686
4128
41770_at
41771_g_at
41772_at
8166925
A_23_P83857
A_33_P3242543
GE62589
GE88131
GO:0003674
GO:0005515
GO:0005575
GO:0005622
GO:0005737
GO:0005739
GO:0005741
GO:0005829
GO:0006576
GO:0006584
GO:0007165
GO:0008131
GO:0008150
GO:0009056
GO:0009967
GO:0016020
GO:0016021
GO:0016491
GO:0019221
GO:0034641
GO:0042133
GO:0042135
GO:0042420
GO:0043226
GO:0055114
Hs.183109.1.S1_3p_at
ILMN_1663640
ILMN_1883352
ILMN_3238159
M68840_at
PH_hs_0010802
PH_hs_0035203
TC0X000207.hg
g4557734_3p_a_at
Participant Of
hasComponent
MAOA Q296*:FAD [mitochondrial outer membrane]
Other forms of this molecule
MAOA [mitochondrial outer membrane]
Modified Residues
Name
L-glutamine 296 replaced with unknown
Coordinate
296
PsiMod
L-glutamine removal [MOD:01637]
A protein modification that effectively removes or replaces an L-glutamine.
Disease
Name
Identifier
Synonyms
disease of mental health
150
Cross References
RefSeq
NP_000231.1
,
NP_001257387.1
ZINC - World Drugs
AOFA_HUMAN
OpenTargets
ENSG00000189221
ZINC - FDA approved
AOFA_HUMAN
ZINC - Substances
AOFA_HUMAN
ZINC target
P21397
ZINC - Biogenic
AOFA_HUMAN
PRO
P21397
PDB
1H8Q
,
2Z5Y
,
2Z5X
,
2BXS
,
2BXR
ZINC - Investigational
AOFA_HUMAN
ZINC - Metabolites
AOFA_HUMAN
GeneCards
P21397
HPA
ENSG00000189221-MAOA
Ensembl
ENST00000542639
,
ENSP00000440846
,
ENST00000338702
,
ENSG00000189221
,
ENSP00000340684
Orphanet
16376
ZINC - Predictions - Purchasable
AOFA_HUMAN
HMDB Protein
HMDBP00169
Interactors (1)
Accession
#Entities
Entities
Confidence Score
Evidence (IntAct)
UniProt:P27338 MAOB
1
MAOB [mitochondrial outer membrane]
(R-HSA-141194)
0.564
2
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