Fusion gene information | Fusion gene name: MAOA_ACTB |
Fusion gene ID: 20774 | | Hgene | Tgene | Gene symbol | MAOA | ACTB | Gene ID | 4128 | 60 | Gene name | monoamine oxidase A | actin beta |
Synonyms | BRNRS|MAO-A | BRWS1|PS1TP5BP1 |
Cytomap | Xp11.3 | 7p22.1 |
Type of gene | protein-coding | protein-coding |
Description | amine oxidase [flavin-containing] Amonoamine oxidase type A | actin, cytoplasmic 1I(2)-actinPS1TP5-binding protein 1beta cytoskeletal actin |
Modification date | 20180519 | 20180522 |
UniProtAcc | P21397 | P60709 |
Ensembl transtripts involved in fusion gene | ENST00000338702, ENST00000542639, ENST00000497485, | ENST00000464611, ENST00000331789, |
Fusion gene scores | * DoF score | 3 X 3 X 1=9 | 10 X 10 X 3=300 |
# samples | 3 | 11 |
** MAII score | log2(3/9*10)=1.73696559416621 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(11/300*10)=-1.44745897697122 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 |
Context | PubMed: MAOA [Title/Abstract] AND ACTB [Title/Abstract] AND fusion [Title/Abstract] |
Functional or gene categories assigned by FusionGDB annotation | |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | MAOA | P21397 | DB00780 | Phenelzine | Amine oxidase [flavin-containing] A | small molecule | approved |
Hgene | MAOA | P21397 | DB00805 | Minaprine | Amine oxidase [flavin-containing] A | small molecule | approved |
Hgene | MAOA | P21397 | DB01247 | Isocarboxazid | Amine oxidase [flavin-containing] A | small molecule | approved |
Hgene | MAOA | P21397 | DB01626 | Pargyline | Amine oxidase [flavin-containing] A | small molecule | approved |
Hgene | MAOA | P21397 | DB09245 | Toloxatone | Amine oxidase [flavin-containing] A | small molecule | approved |
Hgene | MAOA | P21397 | DB00191 | Phentermine | Amine oxidase [flavin-containing] A | small molecule | approved|illicit |
Hgene | MAOA | P21397 | DB01577 | Methamphetamine | Amine oxidase [flavin-containing] A | small molecule | approved|illicit |
Hgene | MAOA | P21397 | DB00182 | Amphetamine | Amine oxidase [flavin-containing] A | small molecule | approved|illicit|investigational |
Hgene | MAOA | P21397 | DB00752 | Tranylcypromine | Amine oxidase [flavin-containing] A | small molecule | approved|investigational |
Hgene | MAOA | P21397 | DB00909 | Zonisamide | Amine oxidase [flavin-containing] A | small molecule | approved|investigational |
Hgene | MAOA | P21397 | DB01168 | Procarbazine | Amine oxidase [flavin-containing] A | small molecule | approved|investigational |
Hgene | MAOA | P21397 | DB01171 | Moclobemide | Amine oxidase [flavin-containing] A | small molecule | approved|investigational |
Hgene | MAOA | P21397 | DB01171 | Moclobemide | Amine oxidase [flavin-containing] A | small molecule | approved|investigational |
Hgene | MAOA | P21397 | DB00721 | Procaine | Amine oxidase [flavin-containing] A | small molecule | approved|investigational|vet_approved |
Hgene | MAOA | P21397 | DB01037 | Selegiline | Amine oxidase [flavin-containing] A | small molecule | approved|investigational|vet_approved |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | MAOA | C0001973 | Alcoholic Intoxication, Chronic | 5 | PSYGENET |
Hgene | MAOA | C0005586 | Bipolar Disorder | 5 | PSYGENET |
Hgene | MAOA | C0011570 | Mental Depression | 5 | PSYGENET |
Hgene | MAOA | C0011581 | Depressive disorder | 5 | PSYGENET |
Hgene | MAOA | C0041696 | Unipolar Depression | 5 | PSYGENET |
Hgene | MAOA | C0525045 | Mood Disorders | 5 | PSYGENET |
Hgene | MAOA | C1269683 | Major Depressive Disorder | 5 | PSYGENET |
Hgene | MAOA | C0003431 | Antisocial Personality Disorder | 3 | CTD_human |
Hgene | MAOA | C0004352 | Autistic Disorder | 3 | CTD_human;HPO |
Hgene | MAOA | C0019151 | Hepatic Encephalopathy | 3 | CTD_human |
Hgene | MAOA | C0036341 | Schizophrenia | 2 | PSYGENET |
Hgene | MAOA | C0085762 | Alcohol abuse | 2 | PSYGENET |
Hgene | MAOA | C0270458 | Severe major depression with psychotic features | 2 | PSYGENET |
Hgene | MAOA | C2362914 | clinical depression | 2 | PSYGENET |
Hgene | MAOA | C0004936 | Mental disorders | 1 | CTD_human |
Hgene | MAOA | C0005587 | Depression, Bipolar | 1 | PSYGENET |
Hgene | MAOA | C0009241 | Cognition Disorders | 1 | CTD_human |
Hgene | MAOA | C0013415 | Dysthymic Disorder | 1 | PSYGENET |
Hgene | MAOA | C0014175 | Endometriosis | 1 | CTD_human |
Hgene | MAOA | C0020179 | Huntington Disease | 1 | CTD_human |
Hgene | MAOA | C0020649 | Hypotension | 1 | CTD_human |
Hgene | MAOA | C0026848 | Myopathy | 1 | CTD_human |
Hgene | MAOA | C0030567 | Parkinson Disease | 1 | CTD_human |
Hgene | MAOA | C0031511 | Pheochromocytoma | 1 | CTD_human |
Hgene | MAOA | C0033054 | Prenatal Exposure Delayed Effects | 1 | CTD_human |
Hgene | MAOA | C0033975 | Psychotic Disorders | 1 | PSYGENET |
Hgene | MAOA | C0600427 | Cocaine Dependence | 1 | PSYGENET |
Hgene | MAOA | C0745744 | End Stage Liver Disease | 1 | CTD_human |
Hgene | MAOA | C1136249 | Mental Retardation, X-Linked | 1 | CTD_human |
Hgene | MAOA | C1285261 | Fetal Nutrition Disorders | 1 | CTD_human |
Hgene | MAOA | C2063866 | Depressive Disorder, Treatment-Resistant | 1 | PSYGENET |
Tgene | ACTB | C2239176 | Liver carcinoma | 2 | CTD_human |
Tgene | ACTB | C0005586 | Bipolar Disorder | 1 | PSYGENET |
Tgene | ACTB | C0009363 | Congenital ocular coloboma (disorder) | 1 | CTD_human |
Tgene | ACTB | C0013393 | Dysostoses | 1 | CTD_human |
Tgene | ACTB | C0013421 | Dystonia | 1 | CTD_human |
Tgene | ACTB | C0014859 | Esophageal Neoplasms | 1 | CTD_human |
Tgene | ACTB | C0018784 | Sensorineural Hearing Loss (disorder) | 1 | CTD_human;HPO |
Tgene | ACTB | C0024121 | Lung Neoplasms | 1 | CTD_human |
Tgene | ACTB | C0024667 | Animal Mammary Neoplasms | 1 | CTD_human |
Tgene | ACTB | C0024668 | Mammary Neoplasms, Experimental | 1 | CTD_human |
Tgene | ACTB | C0027626 | Neoplasm Invasiveness | 1 | CTD_human |
Tgene | ACTB | C0029408 | Degenerative polyarthritis | 1 | CTD_human |
Tgene | ACTB | C0036341 | Schizophrenia | 1 | PSYGENET |
Tgene | ACTB | C0151744 | Myocardial Ischemia | 1 | CTD_human |
Tgene | ACTB | C0242184 | Hypoxia | 1 | CTD_human |
Tgene | ACTB | C0376634 | Craniofacial Abnormalities | 1 | CTD_human |
Tgene | ACTB | C0497552 | Congenital neurologic anomalies | 1 | CTD_human |
Tgene | ACTB | C1846331 | Juvenile-onset dystonia | 1 | CTD_human;ORPHANET;UNIPROT |
Tgene | ACTB | C1855722 | Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation | 1 | ORPHANET;UNIPROT |