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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **1351 - 1375** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
811	calreticulin	CALR Aliases: CRT FLJ26680 RO SSA Sicca syndrome antigen A (autoantigen Ro; calreticulin) autoantigen Ro cC1qR calregulin	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Barrett's esophagus Behcet's disease Budd-Chiari syndrome Burkitt lymphoma Chagas disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kuhnt-Junius degeneration Lyme disease Meckel syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Pick's disease Reye syndrome Richter's syndrome Sjogren's syndrome St. Louis encephalitis T-cell acute lymphoblastic leukemia Weissenbacher-Zweymuller syndrome Wilson disease abdominal obesity-metabolic syndrome 1 achalasia acquired von Willebrand syndrome acrodermatitis acromegaly actinic keratosis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adenosquamous carcinoma adult lymphoma adult medulloblastoma age related macular degeneration aggressive systemic mastocytosis ampulla of Vater benign neoplasm amyotrophic lateral sclerosis anaplastic astrocytoma anemia anthrax disease antiphospholipid syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation atrioventricular block autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant polycystic kidney disease bacterial infectious disease bacterial sepsis benign ependymoma benign mesothelioma bipolar disorder bladder carcinoma bone inflammation disease bone marrow cancer bone osteosarcoma breast cancer breast carcinoma bronchiectasis bronchus cancer bronchus carcinoma bulimia nervosa cancer carcinoma cardiac arrest cardiac sarcoidosis cardiomyopathy cardiovascular system disease cat-scratch disease catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cavernous hemangioma cellular ependymoma central nervous system cancer central nervous system lymphoma cerebral creatine deficiency syndrome 1 cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood disintegrative disease childhood ependymoma childhood leukemia childhood medulloblastoma childhood osteosarcoma cholangiocarcinoma chorioangioma chromophobe renal cell carcinoma chronic lymphocytic leukemia chronic myeloid leukemia chronic neutrophilic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency congenital heart block congenital secretory sodium diarrhea 3 congenital secretory sodium diarrhea 8 congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cyclic hematopoiesis cystic fibrosis cystoid macular edema dedifferentiated liposarcoma degeneration of macula and posterior pole delusional disorder dental caries dentin caries depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma drug psychosis dysthymic disorder eclampsia embryoma endocarditis endometrial cancer endometrial carcinoma endomyocardial fibrosis enthesopathy esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial adenomatous polyposis 1 familial adenomatous polyposis familial hypertrophic cardiomyopathy familial nephrotic syndrome fibrillary astrocytoma fibromyalgia follicular adenoma gallbladder cancer gastroenteritis gastroesophageal reflux disease gastrointestinal system cancer gemistocytic astrocytoma germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor glycogen storage disease II glycoproteinosis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease heart valve disease hemangioma hematologic cancer hematopoietic system disease hemochromatosis type 1 hemochromatosis hepatitis A hepatitis B hepatitis hepatocellular carcinoma high grade glioma histiocytoid hemangioma hyperpituitarism hypertension hyperthyroidism hypertrophic cardiomyopathy hypopharynx cancer ileitis ileocolitis immune system disease inclusion conjunctivitis indolent systemic mastocytosis inflammatory bowel disease intellectual disability intermittent claudication intrahepatic cholangiocarcinoma intramuscular hemangioma iron metabolism disease islet cell tumor juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma keratoconjunctivitis sicca kidney disease kwashiorkor large intestine cancer laryngeal disease learning disability left bundle branch hemiblock leukemia lichen disease lipoid nephrosis liposarcoma liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphangioma lymphoma macrocytic anemia macular degeneration macular retinal edema major depressive disorder malignant astrocytoma malignant mesothelioma marasmus mastocytosis medulloblastoma medullomyoblastoma megaesophagus melancholic depression melanoma melanotic medulloblastoma melioidosis microcystic adenoma microphthalmia mixed glioma mucolipidosis II alpha/beta myelodysplastic syndrome myelofibrosis myeloproliferative neoplasm myocardial infarction myxopapillary ependymoma nasopharynx carcinoma nephritis nephroblastoma nephrosis nephrotic syndrome neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neurotic disorder nonpapillary renal cell carcinoma nutrition disease obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete ymphosarcoma oculocutaneous albinism type IA oculocutaneous albinism onchocerciasis oral squamous cell carcinoma oral submucous fibrosis osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma ovary serous adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma pancytopenia papillary adenoma papillary ependymoma papillary renal cell carcinoma papilloma paranoid schizophrenia parotitis peptic esophagitis periodontitis peripheral vascular disease piebaldism pilocytic astrocytoma pineal region germinoma placental insufficiency plasmacytoma pleomorphic liposarcoma pneumonia polycythemia vera polycythemia portal hypertension post-traumatic stress disorder pre-eclampsia primary immunodeficiency disease proctitis progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma psychotic disorder purpura pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal disease retinal vascular occlusion retinitis rheumatoid arthritis rosacea sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder severe acute respiratory syndrome sialadenitis sick sinus syndrome sideroblastic anemia silent myocardial infarction skin melanoma speech disorder spinal muscular atrophy squamous cell carcinoma squamous cell papilloma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic lupus erythematosus systemic mastocytosis tanycytic ependymoma thrombocytosis thrombophilia thyroiditis thyrotoxicosis tongue cancer tongue squamous cell carcinoma tracheal disease transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trypanosomiasis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ureteral obstruction urinary bladder cancer uterine corpus cancer varicose veins vasculitis vertebrobasilar insufficiency viral infectious disease vitamin B12 deficiency vitiligo
93589	calcium voltage-gated channel auxiliary subunit alpha2delta 4	CACNA2D4 Aliases: alpha2delta-4	Homo sapiens (human)	achromatopsia acquired color blindness acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness blue color blindness borderline personality disorder color blindness cone dystrophy cone-rod dystrophy 2 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness disease of mental health dissociated nystagmus eye disease human immunodeficiency virus infectious disease hypertropia intermittent explosive disorder mechanical strabismus night blindness obsolete asthenopia ophthalmoplegia pathologic nystagmus psychotic disorder red color blindness red-green color blindness retinal cone dystrophy 4 spontaneous ocular nystagmus strabismus
55799	calcium voltage-gated channel auxiliary subunit alpha2delta 3	CACNA2D3 Aliases: HSA272268 alpha2delta-3	Homo sapiens (human)	acute myeloid leukemia anemia breast cancer breast carcinoma cancer carcinoma central nervous system cancer deficiency anemia embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma gliosarcoma heart conduction disease high grade glioma hypochromic anemia lung squamous cell carcinoma macrocytic anemia microcytic anemia mixed glioma nasopharynx carcinoma nicotine dependence prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia stomach cancer stomach carcinoma uterine corpus cancer
9254	calcium voltage-gated channel auxiliary subunit alpha2delta 2	CACNA2D2 Aliases: KIAA0558 alpha2delta-2 gene 26	Homo sapiens (human)	absence epilepsy agnosia alternating hemiplegia of childhood autonomic neuropathy bipolar I disorder brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system disease cerebellar ataxia cerebellar disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood absence epilepsy choreatic disease colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 21 dissociated nystagmus embryoma epilepsy hypertropia idiopathic generalized epilepsy large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma maple syrup urine disease mechanical strabismus nasopharynx carcinoma nervous system disease ophthalmoplegia pathologic nystagmus primary cutaneous amyloidosis prostate cancer prostate carcinoma sensorineural hearing loss sick sinus syndrome spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability type 10
781	calcium voltage-gated channel auxiliary subunit alpha2delta 1	CACNA2D1 Aliases: alpha2delta-1 lncRNA-N3	Homo sapiens (human)	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome West syndrome Williams-Beuren syndrome acute myeloid leukemia amelogenesis imperfecta type 1G atrial fibrillation atrioventricular block azoospermia brain infarction cancer cardiac arrest colon cancer colonic benign neoplasm colorectal cancer depressive disorder developmental and epileptic encephalopathy 110 embryoma epilepsy essential hypertension glaucoma hepatocellular carcinoma hypertension idiopathic scoliosis intellectual disability large intestine cancer learning disability liver cancer major depressive disorder malignant hyperthermia melancholic depression neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia primary open angle glaucoma short QT syndrome sick sinus syndrome stomach cancer stomach carcinoma supravalvular aortic stenosis uveal melanoma
762	carbonic anhydrase 4	CA4 Aliases: CAIV Car4	Homo sapiens (human)	Behcet's disease Zollinger-Ellison syndrome achromatopsia acquired color blindness blindness blue color blindness brain cancer cancer cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease diabetes mellitus dissociated nystagmus eye disease fundus albipunctatus glaucoma hyperinsulinism hypogonadism intellectual disability keratoconus large intestine cancer learning disability lung cancer lung non-small cell carcinoma myocarditis night blindness nonpapillary renal cell carcinoma obesity obsolete asthenopia ophthalmoplegia optic atrophy papillary renal cell carcinoma pathologic nystagmus red color blindness red-green color blindness renal carcinoma renal cell carcinoma retinitis pigmentosa 17 retinitis pigmentosa sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus type 2 diabetes mellitus
140873	chromosome 20 open reading frame 173	C20orf173 Aliases: dJ477O4.4	Homo sapiens (human)
388581	C1q and TNF related 12	C1QTNF12	Homo sapiens (human)
728819	C1GALT1 specific chaperone 1 like	C1GALT1C1L	Homo sapiens (human)
29071	C1GALT1 specific chaperone 1	C1GALT1C1 Aliases: C1GALT2 COSMC	Homo sapiens (human)	IgA glomerulonephritis Tn polyagglutination syndrome angioma serpiginosum autoimmune disease autoimmune lymphoproliferative syndrome cancer capillary hemangioma cavernous hemangioma chorioangioma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma endometrial cancer endometrial carcinoma glomerulonephritis glomus tumor hemangioma hemolytic-uremic syndrome hepatocellular carcinoma histiocytoid hemangioma immune system disease inflammatory bowel disease intramuscular hemangioma kidney disease large intestine cancer liver cancer lymphangioma microphthalmia nephritis nephrosis obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma pyoureter uterine corpus cancer vitiligo
56913	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	C1GALT1 Aliases: C1GALT T-synthase core 1 beta3-Gal-T	Homo sapiens (human)	Henoch-Schoenlein purpura IgA glomerulonephritis Tn polyagglutination syndrome adenocarcinoma adenoma autoimmune disease of blood autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer carcinoma cardiovascular system disease chronic obstructive pulmonary disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma diabetes mellitus embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatocellular carcinoma hypersensitivity vasculitis immune system disease kidney disease large intestine cancer liver cancer microphthalmia nephritis nephrosis obsolete Matthew-Wood syndrome ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma pyoureter sarcomatoid carcinoma thrombocytopenia tubular adenocarcinoma type 2 diabetes mellitus
684	bone marrow stromal cell antigen 2	BST2 Aliases: BST-2 CD317 HM1.24 antiviral factor tetherin tetherin	Homo sapiens (human)	Burkitt lymphoma Down syndrome Ebola hemorrhagic fever Japanese encephalitis Sjogren's syndrome acquired immunodeficiency syndrome alternating hemiplegia of childhood anaplastic astrocytoma angioedema arthritis arthropathy autonomic neuropathy bladder carcinoma brain cancer breast cancer breast carcinoma cancer central nervous system disease chikungunya childhood cerebral astrocytoma childhood leukemia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma conduct disorder dengue disease dengue hemorrhagic fever embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma exanthem fibrillary astrocytoma gemistocytic astrocytoma head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease influenza juvenile pilocytic astrocytoma kwashiorkor large intestine cancer leukemia liver cancer lupus erythematosus malignant astrocytoma marasmus melanoma multiple myeloma multiple sclerosis nasopharynx carcinoma nervous system disease nonpapillary renal cell carcinoma nutrition disease oral squamous cell carcinoma osteoarthritis papillary renal cell carcinoma parapsoriasis peeling skin syndrome pilocytic astrocytoma primary immunodeficiency disease protein-energy malnutrition protoplasmic astrocytoma psoriasis pustulosis of palm and sole renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma scleroderma severe acute respiratory syndrome skin disease skin melanoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic lupus erythematosus systemic scleroderma transitional cell carcinoma urinary bladder cancer urticaria uterine corpus cancer viral infectious disease yellow fever
683	bone marrow stromal cell antigen 1	BST1 Aliases: ADP-ribosyl cyclase 2 BST-1 CD157 NAD(+) nucleosidase cADPR2 cyclic ADP-ribose hydrolase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Burkitt lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome acute monocytic leukemia acute myeloid leukemia allergic asthma asthma autism spectrum disorder autistic disorder benign mesothelioma benign pleural mesothelioma bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic lymphocytic leukemia depressive disorder dysthymic disorder embryoma essential hypertension hypertension inflammatory and toxic neuropathy intrinsic asthma lung benign neoplasm lung cancer lung carcinoma lung disease major depressive disorder malignant mesothelioma malignant pleural mesothelioma melancholic depression neurotic disorder obsolete melancholia ovarian cancer ovarian carcinoma paroxysmal nocturnal hemoglobinuria pleural tuberculosis pneumonia prion disease prostate cancer prostate carcinoma tuberculosis
680	bombesin receptor subtype 3	BRS3	Homo sapiens (human)
221927	BRCA1 associated ATM activator 1	BRAT1	Homo sapiens (human)
673	B-Raf proto-oncogene, serine/threonine kinase	BRAF	Homo sapiens (human)	Langerhans-cell histiocytosis Noonan syndrome 7 Noonan syndrome with multiple lentigines 3 bile duct adenoma cancer cardiofaciocutaneous syndrome 1 cardiofaciocutaneous syndrome cardiomyopathy cholangiocarcinoma colon carcinoma colorectal adenocarcinoma colorectal cancer dysembryoplastic neuroepithelial tumor endometrial carcinoma familial melanoma germinoma high grade glioma intrahepatic cholangiocarcinoma lung cancer malignant astrocytoma melanoma pancreatic acinar cell adenocarcinoma pancreatic cancer pleomorphic xanthoastrocytoma prostate adenocarcinoma thyroid gland papillary carcinoma
670	biphenyl hydrolase like	BPHL Aliases: Bph-rp VACVase breast epithelial mucin-associated antigen valacyclovir hydrolase	Homo sapiens (human)	bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood leukemia childhood osteosarcoma colon carcinoma colorectal cancer embryoma leukemia lung benign neoplasm lung cancer lung carcinoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
669	bisphosphoglycerate mutase	BPGM	Homo sapiens (human)	acquired polycythemia cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis erythropoietin polycythemia familial erythrocytosis 2 familial erythrocytosis 8 normocytic anemia polycythemia vera polycythemia stress polycythemia
56898	3-hydroxybutyrate dehydrogenase 2	BDH2 Aliases: FLJ13261 PRO20933 SDR15C1 UCPA-OR UNQ6308 short chain dehydrogenase/reductase family 15C, member 1	Homo sapiens (human)	anaplastic astrocytoma breast cancer cancer childhood cerebral astrocytoma esophageal cancer esophageal carcinoma fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma juvenile pilocytic astrocytoma liver cancer lupus erythematosus malignant astrocytoma microcytic anemia nasopharynx carcinoma ovarian cancer ovarian carcinoma pilocytic astrocytoma protoplasmic astrocytoma subependymal giant cell astrocytoma systemic lupus erythematosus
622	3-hydroxybutyrate dehydrogenase 1	BDH1 Aliases: SDR9C1 short chain dehydrogenase/reductase family 9C, member 1	Homo sapiens (human)	COVID-19 Graves' disease X-linked dilated cardiomyopathy breast cancer cancer central nervous system cancer congestive heart failure dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy gliosarcoma hepatitis high grade glioma hyperthyroidism mixed glioma nicotine dependence thyrotoxicosis
594	branched chain keto acid dehydrogenase E1 subunit beta	BCKDHB Aliases: 2-oxoisovalerate dehydrogenase subunit beta, mitochondrial maple syrup urine disease	Homo sapiens (human)	Alzheimer's disease 12 Kaposi's sarcoma acute pancreatitis androgen insensitivity syndrome brain edema cancer celiac disease embryoma epilepsy hepatitis B hepatocellular carcinoma hypoglycemia intellectual disability lactic acidosis learning disability liver cancer maple syrup urine disease pancreatic cancer pancreatic carcinoma pancreatitis premature menopause primary ovarian insufficiency systemic lupus erythematosus thyroid gland anaplastic carcinoma visual epilepsy
593	branched chain keto acid dehydrogenase E1 subunit alpha	BCKDHA Aliases: MSU maple syrup urine disease	Homo sapiens (human)	Crohn's colitis Crohn's disease acute pancreatitis arthritis arthropathy bacterial sepsis brain edema cerebral infarction cerebrovascular disease epilepsy gout hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability lactic acidosis learning disability maple syrup urine disease pancreatitis placental insufficiency shigellosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome ulcerative colitis visual epilepsy
63827	brevican	BCAN Aliases: BEHAB CSPG7 MGC13038 brevican proteoglycan chondroitin sulfate proteoglycan 7	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome bladder carcinoma central nervous system cancer cerebral degeneration giant cell glioblastoma glioblastoma gliosarcoma high grade glioma middle cerebral artery infarction mixed glioma retinitis pigmentosa urinary bladder cancer
572	BCL2 associated agonist of cell death	BAD	Homo sapiens (human)	Alzheimer's disease Parkinsonism acute kidney failure brain ischemia breast cancer colon cancer diabetic neuropathy endometrial cancer gastric ulcer glaucoma high grade glioma hypertension hypothyroidism impotence intermittent claudication lung non-small cell carcinoma macular degeneration middle cerebral artery infarction obesity osteoarthritis pancreatic cancer prostate carcinoma prostatic hypertrophy pulmonary fibrosis renal cell carcinoma traumatic brain injury type 2 diabetes mellitus visual epilepsy
570	bile acid-CoA:amino acid N-acyltransferase	BAAT Aliases: BAT glycine N-choloyltransferase	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Ehlers-Danlos syndrome Graves' disease Hantavirus hemorrhagic fever with renal syndrome Lynch syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma atypical hemolytic-uremic syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bacterial sepsis basal cell carcinoma blood coagulation disease breast cancer breast carcinoma cancer carcinoma cervical cancer cholestasis chondrodysplasia-pseudohermaphroditism syndrome colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism coronary thrombosis diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial adenomatous polyposis 1 familial adenomatous polyposis familial hypercholesterolemia fibroepithelial basal cell carcinoma follicular adenoma giant cell glioblastoma glioblastoma hemolytic-uremic syndrome hepatoblastoma hepatocellular carcinoma high grade glioma hypertension hyperthyroidism hypothyroidism infertility islet cell tumor large intestine cancer lipoma lung cancer lung non-small cell carcinoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma morbid obesity myelodysplastic syndrome myocardial infarction myxedema obesity obsolete inherited blood coagulation disease obsolete steatorrhea obsolete type 1 diabetes mellitus 9 osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteomalacia papillary adenoma pleomorphic lipoma pneumonia polycystic ovary syndrome prostate cancer prostate carcinoma rickets sarcomatoid carcinoma silent myocardial infarction steatotic liver disease stomach cancer stomach carcinoma thrombocytopenia thyroid adenoma thyroid cancer thyroid gland carcinoma thyrotoxicosis tuberculosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uterine corpus cancer von Willebrand's disease 1 von Willebrand's disease 3 von Willebrand's disease

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