MAOA (GeneID: 4128) | Homo sapiens
Description: monoamine oxidase A [Source:HGNC Symbol;Acc:HGNC:6833]
Synonyms: BRNRS, MAO-A
Other ID(s): HGNC:6833, ENSG00000189221
Protein Accession Numbers: ENST00000542639, NP_001257387, ENST00000338702.3, NP_000231, ENST00000338702
Statistics: ClinVar(41) gnomAD(220) COSMIC(286) PTM(9)
ClinVar Pathogenicity of Variations help

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000338702 You are here now! ENST00000542639 NP_000231 You are here now! NP_001257387


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF01593 Amino_oxidase Flavin containing amine oxidoreductase 23-460 CL0063 NADP_Rossmann Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Alcoholic Intoxication, Chronic Chemically-Induced Disorders ; Mental Disorders ; 0.497 0.655
Antisocial Personality Disorder Mental Disorders ; 0.497 0.655
Autistic Disorder Mental Disorders ; 0.497 0.655
Behavior Disorders Mental Disorders ; 0.497 0.655
Mental disorders Mental Disorders ; 0.497 0.655
Bipolar Disorder Mental Disorders ; 0.497 0.655
Depression, Bipolar Mental Disorders ; 0.497 0.655
Malignant neoplasm of breast Neoplasms ; Skin and Connective Tissue Diseases ; 0.497 0.655
Cognition Disorders Mental Disorders ; 0.497 0.655
Mental Depression Behavior and Behavior Mechanisms ; 0.497 0.655
Depressive disorder Mental Disorders ; 0.497 0.655
Dyssocial Behavior Mental Disorders ; 0.497 0.655
Dysthymic Disorder Mental Disorders ; 0.497 0.655
Endometriosis Female Urogenital Diseases and Pregnancy Complications ; 0.497 0.655
Hepatic Coma Digestive System Diseases ; Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.497 0.655
Hepatic Encephalopathy Digestive System Diseases ; Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.497 0.655
Huntington Disease Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Mental Disorders ; 0.497 0.655
Hypotension Cardiovascular Diseases ; 0.497 0.655
Myopathy Musculoskeletal Diseases ; Nervous System Diseases ; 0.497 0.655
Parkinson Disease Nervous System Diseases ; 0.497 0.655
Pheochromocytoma Neoplasms ; 0.497 0.655
Prenatal Exposure Delayed Effects Female Urogenital Diseases and Pregnancy Complications ; 0.497 0.655
Psychotic Disorders Mental Disorders ; 0.497 0.655
Schizophrenia Mental Disorders ; 0.497 0.655
Unipolar Depression Mental Disorders ; 0.497 0.655
Alcohol abuse Chemically-Induced Disorders ; Mental Disorders ; 0.497 0.655
Fetal Malnutrition Female Urogenital Diseases and Pregnancy Complications ; Nutritional and Metabolic Diseases ; 0.497 0.655
Endometrioma Female Urogenital Diseases and Pregnancy Complications ; 0.497 0.655
Severe major depression with psychotic features N/A 0.497 0.655
Diagnosis, Psychiatric Mental Disorders ; 0.497 0.655
Huntington Disease, Late Onset Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Mental Disorders ; 0.497 0.655
Mood Disorders Mental Disorders ; 0.497 0.655
Cocaine Dependence Chemically-Induced Disorders ; Mental Disorders ; 0.497 0.655
End Stage Liver Disease Digestive System Diseases ; 0.497 0.655
Fulminant Hepatic Failure with Cerebral Edema Digestive System Diseases ; Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.497 0.655
Hepatic Stupor Digestive System Diseases ; Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.497 0.655
Akinetic-Rigid Variant of Huntington Disease Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Mental Disorders ; 0.497 0.655
Juvenile Huntington Disease Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Mental Disorders ; 0.497 0.655
Brunner Syndrome Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.497 0.655
Mental Retardation, X-Linked Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.497 0.655
Pheochromocytoma, Extra-Adrenal Neoplasms ; 0.497 0.655
Major Depressive Disorder Mental Disorders ; 0.497 0.655
Fetal Nutrition Disorders Female Urogenital Diseases and Pregnancy Complications ; Nutritional and Metabolic Diseases ; 0.497 0.655
Depressive Disorder, Treatment-Resistant Mental Disorders ; 0.497 0.655
clinical depression N/A 0.497 0.655
Chronic Liver Failure Digestive System Diseases ; 0.497 0.655
Intellectual Disability Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.497 0.655
Mental Disorders, Severe Mental Disorders ; 0.497 0.655
NO RESULT FOUND
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