Fusion gene information | Fusion gene name: ALB-ARMC3 |
Fusion gene ID: hg213tg219681 | | Hgene | Tgene | Gene symbol | ALB | ARMC3 | Gene ID | 213 | 219681 | Gene name | albumin | armadillo repeat containing 3 |
Synonyms | HSA|PRO0883|PRO0903|PRO1341 | CT81|KU-CT-1 |
Cytomap | ('ALB')('ARMC3') 4q13.3 | 10p12.2 |
Type of gene | protein-coding | protein-coding |
Description | serum albumin | armadillo repeat-containing protein 3beta-catenin-like proteincancer/testis antigen 81 |
Modification date | 20200329 | 20200313 |
UniProtAcc | . | Q5W041 |
Ensembl transtripts involved in fusion gene | ENST00000295897, ENST00000415165, ENST00000401494, ENST00000503124, ENST00000505649, ENST00000509063,
| |
Fusion gene scores | * DoF score | 66 X 51 X 5=16830 | 6 X 10 X 5=300 |
# samples | 74 | 9 |
** MAII score | log2(74/16830*10)=-4.507366095701 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(9/300*10)=-1.73696559416621 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 |
Context | PubMed: ALB [Title/Abstract] AND ARMC3 [Title/Abstract] AND fusion [Title/Abstract] |
Most frequent breakpoint | ALB(74286973)-ARMC3(23274006), # samples:1
|
Anticipated loss of major functional domain due to fusion event. | |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ALB | C0033687 | Proteinuria | 9 | CTD_human |
Hgene | ALB | C0017658 | Glomerulonephritis | 8 | CTD_human |
Hgene | ALB | C0022658 | Kidney Diseases | 8 | CTD_human |
Hgene | ALB | C1704377 | Bright Disease | 8 | CTD_human |
Hgene | ALB | C0017665 | Membranous glomerulonephritis | 6 | CTD_human |
Hgene | ALB | C0027697 | Nephritis | 6 | CTD_human |
Hgene | ALB | C0086445 | Idiopathic Membranous Glomerulonephritis | 6 | CTD_human |
Hgene | ALB | C0342185 | Hyperthyroxinemia, Familial Dysalbuminemic | 6 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
Hgene | ALB | C1704378 | Heymann Nephritis | 6 | CTD_human |
Hgene | ALB | C0022660 | Kidney Failure, Acute | 4 | CTD_human |
Hgene | ALB | C0027707 | Nephritis, Interstitial | 4 | CTD_human |
Hgene | ALB | C0038454 | Cerebrovascular accident | 4 | CTD_human |
Hgene | ALB | C0041349 | Nephritis, Tubulointerstitial | 4 | CTD_human |
Hgene | ALB | C0751956 | Acute Cerebrovascular Accidents | 4 | CTD_human |
Hgene | ALB | C1565662 | Acute Kidney Insufficiency | 4 | CTD_human |
Hgene | ALB | C2609414 | Acute kidney injury | 4 | CTD_human |
Hgene | ALB | C0023893 | Liver Cirrhosis, Experimental | 3 | CTD_human |
Hgene | ALB | C0025290 | Aseptic Meningitis | 3 | CTD_human |
Hgene | ALB | C0013221 | Drug toxicity | 2 | CTD_human |
Hgene | ALB | C0014544 | Epilepsy | 2 | CTD_human |
Hgene | ALB | C0019193 | Hepatitis, Toxic | 2 | CTD_human |
Hgene | ALB | C0020649 | Hypotension | 2 | CTD_human |
Hgene | ALB | C0023890 | Liver Cirrhosis | 2 | CTD_human |
Hgene | ALB | C0027726 | Nephrotic Syndrome | 2 | CTD_human |
Hgene | ALB | C0036830 | Serum Sickness | 2 | CTD_human |
Hgene | ALB | C0041755 | Adverse reaction to drug | 2 | CTD_human |
Hgene | ALB | C0086237 | Epilepsy, Cryptogenic | 2 | CTD_human |
Hgene | ALB | C0162557 | Liver Failure, Acute | 2 | CTD_human |
Hgene | ALB | C0236018 | Aura | 2 | CTD_human |
Hgene | ALB | C0239946 | Fibrosis, Liver | 2 | CTD_human |
Hgene | ALB | C0751111 | Awakening Epilepsy | 2 | CTD_human |
Hgene | ALB | C0860207 | Drug-Induced Liver Disease | 2 | CTD_human |
Hgene | ALB | C0878666 | Analbuminemia | 2 | ORPHANET |
Hgene | ALB | C1262760 | Hepatitis, Drug-Induced | 2 | CTD_human |
Hgene | ALB | C3658290 | Drug-Induced Acute Liver Injury | 2 | CTD_human |
Hgene | ALB | C4277682 | Chemical and Drug Induced Liver Injury | 2 | CTD_human |
Hgene | ALB | C4279912 | Chemically-Induced Liver Toxicity | 2 | CTD_human |
Hgene | ALB | C0002994 | Angioedema | 1 | CTD_human |
Hgene | ALB | C0003460 | Anuria | 1 | CTD_human |
Hgene | ALB | C0003865 | Arthritis, Adjuvant-Induced | 1 | CTD_human |
Hgene | ALB | C0004509 | Azoospermia | 1 | CTD_human |
Hgene | ALB | C0005398 | Cholestasis, Extrahepatic | 1 | CTD_human |
Hgene | ALB | C0006111 | Brain Diseases | 1 | CTD_human |
Hgene | ALB | C0007222 | Cardiovascular Diseases | 1 | CTD_human |
Hgene | ALB | C0007786 | Brain Ischemia | 1 | CTD_human |
Hgene | ALB | C0008312 | Primary biliary cirrhosis | 1 | CTD_human |
Hgene | ALB | C0011573 | Endogenous depression | 1 | CTD_human |
Hgene | ALB | C0011581 | Depressive disorder | 1 | CTD_human |
Hgene | ALB | C0011875 | Diabetic Angiopathies | 1 | CTD_human |
Hgene | ALB | C0011881 | Diabetic Nephropathy | 1 | CTD_human |
Hgene | ALB | C0013502 | Echinococcosis | 1 | CTD_human |
Hgene | ALB | C0014518 | Toxic Epidermal Necrolysis | 1 | CTD_human |
Hgene | ALB | C0016059 | Fibrosis | 1 | CTD_human |
Hgene | ALB | C0017662 | Glomerulonephritis, Membranoproliferative | 1 | CTD_human |
Hgene | ALB | C0017667 | Nodular glomerulosclerosis | 1 | CTD_human |
Hgene | ALB | C0018799 | Heart Diseases | 1 | CTD_human |
Hgene | ALB | C0018801 | Heart failure | 1 | CTD_human |
Hgene | ALB | C0018802 | Congestive heart failure | 1 | CTD_human |
Hgene | ALB | C0019061 | Hemolytic-Uremic Syndrome | 1 | CTD_human |
Hgene | ALB | C0019158 | Hepatitis | 1 | CTD_human |
Hgene | ALB | C0019209 | Hepatomegaly | 1 | CTD_human |
Hgene | ALB | C0019693 | HIV Infections | 1 | CTD_human |
Hgene | ALB | C0019699 | HIV Seropositivity | 1 | CTD_human |
Hgene | ALB | C0020517 | Hypersensitivity | 1 | CTD_human |
Hgene | ALB | C0020522 | Delayed Hypersensitivity | 1 | CTD_human |
Hgene | ALB | C0020538 | Hypertensive disease | 1 | CTD_human |
Hgene | ALB | C0022548 | Keloid | 1 | CTD_human |
Hgene | ALB | C0022661 | Kidney Failure, Chronic | 1 | CTD_human |
Hgene | ALB | C0023212 | Left-Sided Heart Failure | 1 | CTD_human |
Hgene | ALB | C0023892 | Biliary cirrhosis | 1 | CTD_human |
Hgene | ALB | C0024623 | Malignant neoplasm of stomach | 1 | CTD_human |
Hgene | ALB | C0025193 | Melancholia | 1 | CTD_human |
Hgene | ALB | C0025945 | Microangiopathy, Diabetic | 1 | CTD_human |
Hgene | ALB | C0026848 | Myopathy | 1 | CTD_human |
Hgene | ALB | C0027055 | Myocardial Reperfusion Injury | 1 | CTD_human |
Hgene | ALB | C0027720 | Nephrosis | 1 | CTD_human |
Hgene | ALB | C0028797 | Occupational Diseases | 1 | CTD_human |
Hgene | ALB | C0030193 | Pain | 1 | CTD_human |
Hgene | ALB | C0030286 | Pancreatic Diseases | 1 | CTD_human |
Hgene | ALB | C0030305 | Pancreatitis | 1 | CTD_human |
Hgene | ALB | C0035222 | Respiratory Distress Syndrome, Adult | 1 | CTD_human |
Hgene | ALB | C0035242 | Respiratory Tract Diseases | 1 | CTD_human |
Hgene | ALB | C0035457 | Rhinitis, Allergic, Perennial | 1 | CTD_human |
Hgene | ALB | C0038325 | Stevens-Johnson Syndrome | 1 | CTD_human |
Hgene | ALB | C0038356 | Stomach Neoplasms | 1 | CTD_human |
Hgene | ALB | C0040034 | Thrombocytopenia | 1 | CTD_human |
Hgene | ALB | C0041696 | Unipolar Depression | 1 | CTD_human |
Hgene | ALB | C0042109 | Urticaria | 1 | CTD_human |
Hgene | ALB | C0042164 | Uveitis | 1 | CTD_human |
Hgene | ALB | C0085584 | Encephalopathies | 1 | CTD_human |
Hgene | ALB | C0086133 | Depressive Syndrome | 1 | CTD_human |
Hgene | ALB | C0152013 | Adenocarcinoma of lung (disorder) | 1 | CTD_human |
Hgene | ALB | C0234230 | Pain, Burning | 1 | CTD_human |
Hgene | ALB | C0234238 | Ache | 1 | CTD_human |
Hgene | ALB | C0234254 | Radiating pain | 1 | CTD_human |
Hgene | ALB | C0235527 | Heart Failure, Right-Sided | 1 | CTD_human |
Hgene | ALB | C0238065 | Secondary Biliary Cholangitis | 1 | CTD_human |
Hgene | ALB | C0239981 | Hypoalbuminemia | 1 | CTD_human |
Hgene | ALB | C0268742 | Membranoproliferative Glomerulonephritis, Type I | 1 | CTD_human |
Hgene | ALB | C0268743 | Membranoproliferative Glomerulonephritis, Type II | 1 | CTD_human |
Hgene | ALB | C0273115 | Lung Injury | 1 | CTD_human |
Hgene | ALB | C0282126 | Depression, Neurotic | 1 | CTD_human |
Hgene | ALB | C0458257 | Pain, Splitting | 1 | CTD_human |
Hgene | ALB | C0458259 | Pain, Crushing | 1 | CTD_human |
Hgene | ALB | C0751407 | Pain, Migratory | 1 | CTD_human |
Hgene | ALB | C0751408 | Suffering, Physical | 1 | CTD_human |
Hgene | ALB | C0917798 | Cerebral Ischemia | 1 | CTD_human |
Hgene | ALB | C0971858 | Arthritis, Collagen-Induced | 1 | CTD_human |
Hgene | ALB | C0993582 | Arthritis, Experimental | 1 | CTD_human |
Hgene | ALB | C1274933 | Drug-Induced Stevens Johnson Syndrome | 1 | CTD_human |
Hgene | ALB | C1306571 | Hepatic Insufficiency | 1 | CTD_human |
Hgene | ALB | C1527304 | Allergic Reaction | 1 | CTD_human |
Hgene | ALB | C1623038 | Cirrhosis | 1 | CTD_human |
Hgene | ALB | C1708349 | Hereditary Diffuse Gastric Cancer | 1 | CTD_human |
Hgene | ALB | C1720821 | Membranoproliferative Glomerulonephritis, Type III | 1 | CTD_human |
Hgene | ALB | C1959583 | Myocardial Failure | 1 | CTD_human |
Hgene | ALB | C1961112 | Heart Decompensation | 1 | CTD_human |
Hgene | ALB | C2350344 | Chronic Lung Injury | 1 | CTD_human |
Hgene | ALB | C3658301 | Mycoplasma-Induced Stevens-Johnson Syndrome | 1 | CTD_human |
Hgene | ALB | C3658302 | Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum | 1 | CTD_human |
Hgene | ALB | C4505456 | HIV Coinfection | 1 | CTD_human |
Hgene | ALB | C4551595 | Biliary Cirrhosis, Primary, 1 | 1 | CTD_human |
Hgene | ALB | C4553297 | Cystic Echinocccosis | 1 | CTD_human |