MAOB (GeneID: 465588) | Pan troglodytes
Description: monoamine oxidase B [Source:VGNC Symbol;Acc:VGNC:1362]
Synonyms:
Other ID(s): ENSPTRG00000021817
Protein Accession Numbers: XP_009437242, XP_003954020, XP_003317481
Statistics: ClinVar(6) gnomAD(243) COSMIC(296) PTM(19)
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.
ENST00000378069 You are here now! ENST00000536181 ENST00000538942 NP_000889 You are here now!


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 14-451 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 ; 0.575 0.724
Alzheimer's Disease Nervous System Diseases ; Mental Disorders ; 0.575 0.724
Anemia, Megaloblastic Hemic and Lymphatic Diseases ; 0.575 0.724
Autistic Disorder Mental Disorders ; 0.575 0.724
Bipolar Disorder Mental Disorders ; 0.575 0.724
Malignant tumor of colon Neoplasms ; Digestive System Diseases ; 0.575 0.724
Colonic Neoplasms Neoplasms ; Digestive System Diseases ; 0.575 0.724
Presenile dementia Nervous System Diseases ; Mental Disorders ; 0.575 0.724
Mental Depression Behavior and Behavior Mechanisms ; 0.575 0.724
Depressive disorder Mental Disorders ; 0.575 0.724
Endometriosis Female Urogenital Diseases and Pregnancy Complications ; 0.575 0.724
Hepatic Coma Digestive System Diseases ; Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.575 0.724
Hepatic Encephalopathy Digestive System Diseases ; Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.575 0.724
Huntington Disease Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Mental Disorders ; 0.575 0.724
Hypotension Cardiovascular Diseases ; 0.575 0.724
Parkinson Disease Nervous System Diseases ; 0.575 0.724
Pheochromocytoma Neoplasms ; 0.575 0.724
Schizophrenia Mental Disorders ; 0.575 0.724
Unipolar Depression Mental Disorders ; 0.575 0.724
Endometrioma Female Urogenital Diseases and Pregnancy Complications ; 0.575 0.724
Familial Alzheimer Disease (FAD) Nervous System Diseases ; Mental Disorders ; 0.575 0.724
Senile Plaques Pathological Conditions, Signs and Symptoms ; 0.575 0.724
Huntington Disease, Late Onset Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Mental Disorders ; 0.575 0.724
Alzheimer Disease, Late Onset Nervous System Diseases ; Mental Disorders ; 0.575 0.724
Mood Disorders Mental Disorders ; 0.575 0.724
Acute Confusional Senile Dementia Nervous System Diseases ; Mental Disorders ; 0.575 0.724
Alzheimer's Disease, Focal Onset Nervous System Diseases ; Mental Disorders ; 0.575 0.724
Alzheimer Disease, Early Onset Nervous System Diseases ; Mental Disorders ; 0.575 0.724
Fulminant Hepatic Failure with Cerebral Edema Digestive System Diseases ; Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.575 0.724
Hepatic Stupor Digestive System Diseases ; Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.575 0.724
Akinetic-Rigid Variant of Huntington Disease Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Mental Disorders ; 0.575 0.724
Juvenile Huntington Disease Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Mental Disorders ; 0.575 0.724
Pheochromocytoma, Extra-Adrenal Neoplasms ; 0.575 0.724
Major Depressive Disorder Mental Disorders ; 0.575 0.724
Plaque, Amyloid Pathological Conditions, Signs and Symptoms ; 0.575 0.724
Intellectual Disability Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.575 0.724
NO RESULT FOUND
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