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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 **2276 - 2300** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
8694	diacylglycerol O-acyltransferase 1	DGAT1 Aliases: ARGP1	Homo sapiens (human)	Chanarin-Dorfman syndrome alopecia amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive congenital ichthyosis 1 cancer cardiomyopathy celiac disease chronic fatigue syndrome chronic kidney disease chylomicron retention disease congenital diarrhea 5 with tufting enteropathy congenital diarrhea 6 congenital diarrhea 7 with exudative enteropathy congenital malabsorptive diarrhea 4 congenital secretory sodium diarrhea 3 congenital secretory sodium diarrhea 8 congestive heart failure coronary artery disease diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism encephalitis encephalomyelitis familial hyperlipidemia familial lipoprotein lipase deficiency familial nephrotic syndrome familial periodic paralysis gastrointestinal system disease gestational diabetes glucose intolerance hepatitis C hyperlipoproteinemia type V ichthyosis intestinal disease keratosis follicularis kwashiorkor leech infestation lipid metabolism disorder lipoid nephrosis lupus erythematosus marasmus mastitis microvillus inclusion disease mongolian spot myelitis myiasis myopathy nephrotic syndrome nutrition disease obesity obsolete congenital ichthyosiform erythroderma phototoxic dermatitis prediabetes syndrome progressive muscular atrophy prostate cancer prostate carcinoma protein-energy malnutrition protein-losing enteropathy pseudoxanthoma elasticum steatotic liver disease systemic lupus erythematosus toxoplasmosis tropical sprue type 2 diabetes mellitus
80339	patatin like phospholipase domain containing 3	PNPLA3 Aliases: FLJ22012 adiponutrin dJ796I17.1 iPLA2epsilon	Homo sapiens (human)	Chanarin-Dorfman syndrome Phelan-McDermid syndrome Wernicke-Korsakoff syndrome Wilson disease Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acquired metabolic disease acute lymphoblastic leukemia adrenoleukodystrophy adult hepatocellular carcinoma adult liposarcoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis bipolar disorder cancer cardiovascular system disease carotid artery disease celiac disease childhood hepatocellular carcinoma childhood liposarcoma cholecystolithiasis choledocholithiasis cholelithiasis chronic kidney disease congenital hypothyroidism coronary artery disease diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma familial hyperlipidemia gallbladder disease gestational diabetes glucose intolerance heart disease hemochromatosis type 1 hemochromatosis hepatitis B hepatitis C hepatitis hepatocellular carcinoma human immunodeficiency virus infectious disease hyperglycemia hyperinsulinism hypertrophic cardiomyopathy 1 hypothyroidism inflammatory bowel disease intrahepatic cholestasis of pregnancy intrinsic asthma iron metabolism disease kidney failure liposarcoma liver cancer liver carcinoma liver cirrhosis liver disease lymphoblastic lymphoma metabolic dysfunction-associated steatotic liver disease mood disorder morbid obesity myxedema obesity obsolete type 1 diabetes mellitus 9 osteoarthritis pleomorphic liposarcoma polycystic ovary syndrome portal hypertension prediabetes syndrome premenstrual tension primary biliary cholangitis primary sclerosing cholangitis sclerosing cholangitis steatotic liver disease 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 viral infectious disease
1376	carnitine palmitoyltransferase 2	CPT2 Aliases: CPTASE	Homo sapiens (human)	Chanarin-Dorfman syndrome Meckel syndrome Pearson syndrome Reye syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis attention deficit hyperactivity disorder autosomal dominant polycystic kidney disease beta thalassemia brain disease brain edema breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency carnitine palmitoyltransferase II deficiency cataract chronic fatigue syndrome chronic kidney disease clubfoot colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis 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 disease of metabolism embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy essential thrombocythemia familial hyperlipidemia familial periodic paralysis fibromyalgia glycogen storage disease II glycogen storage disease V hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hydronephrosis hyperglycemia hypertrophic cardiomyopathy hypoglycemia influenza isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer lipid metabolism disorder liver cancer liver cirrhosis medium chain acyl-CoA dehydrogenase deficiency microcephaly mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency muscular disease myelitis myelodysplastic syndrome myocardial infarction myoglobinuria myopathy myositis neurogenic arthropathy neuroleptic malignant syndrome obesity ovarian cancer pancytopenia placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma pseudosarcomatous fibromatosis psoriatic arthritis sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction status epilepticus steatotic liver disease systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency viral infectious disease visual epilepsy
9663	lipin 2	LPIN2 Aliases: KIAA0249	Homo sapiens (human)	Chanarin-Dorfman syndrome Crohn's colitis Crohn's disease Diamond-Blackfan anemia SAPHO syndrome acne agranulocytosis allergic asthma anemia asthma autosomal recessive congenital ichthyosis 1 autosomal recessive osteopetrosis 7 cancer chronic recurrent multifocal osteomyelitis congenital dyserythropoietic anemia congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypoplastic anemia congestive heart failure dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism familial mediterranean fever familial periodic paralysis fibromyalgia gastrointestinal system disease glomerulonephritis granular corneal dystrophy 2 ichthyosis inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intrinsic asthma keratosis follicularis leukopenia lipid metabolism disorder lipoatrophic diabetes mellitus lipodystrophy macrocytic anemia mevalonic aciduria microcytic anemia mongolian spot myoglobinuria myopathy myopia myositis nephritis neutropenia obesity obsolete congenital ichthyosiform erythroderma osteomyelitis osteopetrosis osteosclerosis prostate cancer prostate carcinoma proteinuria pseudoxanthoma elasticum relapsing fever rheumatoid arthritis severe congenital neutropenia synovitis tenosynovitis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue type 2 diabetes mellitus ulcerative colitis
22934	ribose 5-phosphate isomerase A	RPIA	Homo sapiens (human)	Chagas disease agnosia cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus critical illness polyneuropathy disease of metabolism dissociated nystagmus epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis hepatocellular carcinoma inflammatory and toxic neuropathy islet cell tumor large intestine cancer liver cancer liver carcinoma meningoencephalitis multiple myeloma neuropathy optic atrophy papillary adenocarcinoma papillary renal cell carcinoma pathologic nystagmus peripheral nervous system disease polyneuropathy spontaneous ocular nystagmus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma trypanosomiasis visual epilepsy
6385	syndecan 4	SDC4 Aliases: SYND4 amphiglycan ryudocan syndecan proteoglycan 4	Homo sapiens (human)	Chagas disease Sezary's disease actinic keratosis acute interstitial pneumonia acute myeloid leukemia acute myocardial infarction allergic asthma anaplastic astrocytoma aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autism spectrum disorder autistic disorder bacterial infectious disease bone osteosarcoma breast cancer breast carcinoma cancer cataract 32 multiple types cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood osteosarcoma chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy embryoma endometriosis of uterus endometriosis fibrillary astrocytoma fibrodysplasia ossificans progressiva gastroenteritis gemistocytic astrocytoma glomerulonephritis hepatitis C high grade glioma hyperglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis intrinsic asthma juvenile pilocytic astrocytoma kidney disease large intestine cancer leprosy liver cirrhosis lung cancer lung non-small cell carcinoma malignant astrocytoma melanoma myocardial infarction myositis ossificans nephritis nephrosis osteoarthritis osteosarcoma papillary adenocarcinoma papillary renal cell carcinoma pilocytic astrocytoma pneumonia postinflammatory pulmonary fibrosis primary cutaneous T-cell non-Hodgkin lymphoma protoplasmic astrocytoma pulmonary fibrosis pyoureter rheumatoid arthritis seborrheic keratosis silent myocardial infarction skin disease skin melanoma subependymal giant cell astrocytoma synovitis tenosynovitis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma trypanosomiasis type 2 diabetes mellitus ureteral obstruction
2645	glucokinase	GCK Aliases: HK4 hexokinase 4	Homo sapiens (human)	Chagas disease Fanconi anemia complementation group C Fanconi anemia Laron syndrome Marfan syndrome Werner syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute chest syndrome adult-onset Still's disease agnosia apraxia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bronchus cancer bronchus carcinoma cancer cardiovascular system disease chronic fatigue syndrome congenital heart disease congenital ptosis coronary artery disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism embryoma encephalitis encephalomyelitis endocrine pancreas disease epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperinsulinemic hypoglycemia 3 generalized anxiety disorder gestational diabetes glomerulonephritis glucose intolerance glucose metabolism disease heart disease hepatocellular carcinoma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia hypoglycemic coma immune system disease insulinoma intellectual disability kidney disease learning disability leishmaniasis liver cancer liver carcinoma liver cirrhosis lung benign neoplasm lung cancer lung carcinoma maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young type 3 maturity-onset diabetes of the young myelitis myotonic dystrophy type 1 myotonic dystrophy type 2 neonatal diabetes nephritis nephrosis neuropathy nutmeg liver obesity obsolete infantile epileptic encephalopathy obsolete type 1 diabetes mellitus 9 osteoarthritis pancreatic cancer pancreatic carcinoma peripheral nervous system disease permanent neonatal diabetes mellitus placental insufficiency polyneuropathy prediabetes syndrome progeria prostate cancer prostate carcinoma ptosis pyoureter retinal disease retinitis rheumatoid arthritis sensorineural hearing loss situs inversus steatotic liver disease syndromic X-linked intellectual disability 94 systemic lupus erythematosus transient neonatal diabetes mellitus trypanosomiasis tuberous sclerosis 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 urea cycle disorder visceral leishmaniasis visual epilepsy
64834	ELOVL fatty acid elongase 1	ELOVL1 Aliases: Ssc1	Homo sapiens (human)	Cauda equina syndrome acanthosis nigricans acrodermatitis adrenoleukodystrophy cancer dermatitis dry eye syndrome hyperglycemia neurogenic bladder obsolete asthenopia xerophthalmia
91949	component of oligomeric golgi complex 7	COG7	Homo sapiens (human)	Cauda equina syndrome Laron syndrome achondroplasia autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis cardiomyopathy cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIe congenital disorder of glycosylation congenital heart disease congestive heart failure endomyocardial fibrosis esophagitis familial hypertrophic cardiomyopathy gastroesophageal reflux disease genetic disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels microcephaly neurogenic bladder obsolete congenital ichthyosiform erythroderma peptic esophagitis placental insufficiency sensorineural hearing loss
55331	alkaline ceramidase 3	ACER3 Aliases: APHC FLJ11238 alkaline phytoceramidase	Homo sapiens (human)	Cauda equina syndrome Laron syndrome achondroplasia acute myeloid leukemia cerebellar ataxia cerebellar disease cerebral degeneration dystonia hepatocellular carcinoma intellectual disability learning disability leukodystrophy liver cancer melanoma metabolic dysfunction-associated steatohepatitis neurogenic bladder neuropathy peripheral nervous system disease skin melanoma
23417	malonyl-CoA decarboxylase	MLYCD Aliases: MCD hMCD	Homo sapiens (human)	Castleman disease Kaposi's sarcoma Kimura disease Laron syndrome Marfan syndrome Meesmann corneal dystrophy Schmid metaphyseal chondrodysplasia Senior-Loken syndrome achondroplasia acquired immunodeficiency syndrome acute kidney tubular necrosis adult lymphoma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome cancer cardiomyopathy central nervous system lymphoma childhood lymphoma choline deficiency disease diabetes mellitus diarrhea endomyocardial fibrosis epilepsy essential hypertension familial hypertrophic cardiomyopathy familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis human immunodeficiency virus infectious disease hypertension hypertrophic cardiomyopathy hypoglycemia inherited metabolic disorder kidney disease lactic acidosis lipoid nephrosis liver cirrhosis lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macular corneal dystrophy membranous glomerulonephritis metabolic dysfunction-associated steatotic liver disease microphthalmia multicentric Castleman disease nasopharynx carcinoma nephritis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis nephrotic syndrome normal pressure hydrocephalus obesity obsolete Matthew-Wood syndrome obsolete constipation obsolete ymphosarcoma oral tuberculosis primary immunodeficiency disease pyoureter situs inversus steatotic liver disease systemic Epstein-Barr virus positive T-cell lymphoma of childhood tuberculosis tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus visual epilepsy
55858	transmembrane protein 165	TMEM165 Aliases: GDT1 SLC64A1 TMPT27 TPA regulated locus TPARL	Homo sapiens (human)	Camurati-Engelmann disease Laron syndrome Marfan syndrome X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 achondroplasia acoustic neuroma amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta cancer cellular schwannoma chondrodysplasia punctata congenital disorder of glycosylation type II congenital disorder of glycosylation type IIk congenital disorder of glycosylation dentin dysplasia dentinogenesis imperfecta embryoma hepatocellular carcinoma isolated elevated serum creatine phosphokinase levels liver cancer melanotic neurilemmoma meningioma neurilemmoma neurofibromatosis osteoporosis pituitary adenoma plexiform schwannoma scoliosis situs inversus tuberous sclerosis vestibular schwannomatosis
6916	thromboxane A synthase 1	TBXAS1 Aliases: CYP5 CYP5A1 THAS TS TXAS TXS cytochrome P450, family 5, subfamily A, polypeptide 1	Homo sapiens (human)	Camurati-Engelmann disease Ghosal hematodiaphyseal syndrome acute myocardial infarction acute necrotizing pancreatitis alcoholic hepatitis alcoholic liver cirrhosis allergic asthma anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma ataxia telangiectasia atherosclerosis autosomal recessive osteopetrosis 7 benign mesothelioma brain infarction brain stem infarction breast cancer breast carcinoma cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis essential hypertension glomerulonephritis heart disease hydronephrosis hypertension inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease liver cirrhosis lung benign neoplasm macrocytic anemia malignant mesothelioma malignant pleural mesothelioma membranous glomerulonephritis myelofibrosis myocardial infarction nephritis osteopetrosis osteosclerosis pancytopenia pituitary adenoma pituitary cancer pituitary carcinoma platelet-type bleeding disorder 14 prostate cancer prostate carcinoma pulmonary embolism schizophrenia silent myocardial infarction speech disorder thrombocytopenia thrombosis ulcerative colitis urinary bladder cancer
1800	dipeptidase 1	DPEP1	Homo sapiens (human)	Camurati-Engelmann disease Crohn's colitis Crohn's disease Duchenne muscular dystrophy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease SAPHO syndrome X-linked lymphoproliferative syndrome 2 adenoma amyloidosis ankylosing spondylitis arthritis arthropathy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bladder calculus bone cancer bone osteosarcoma breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer childhood osteosarcoma cholecystolithiasis choledocholithiasis cholelithiasis chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital muscular dystrophy distal myopathy dystonia embryoma epithelioid leiomyosarcoma essential hypertension facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial hemiplegic migraine 2 familial hemiplegic migraine fibrodysplasia ossificans progressiva focal hand dystonia follicular adenoma generalized dystonia gliosarcoma heart disease hepatoblastoma hepatocellular carcinoma high grade glioma hypertension hyperuricemia inflammatory bowel disease 1 inflammatory bowel disease influenza interstitial nephritis invasive ductal carcinoma large intestine cancer laryngeal disease leiomyosarcoma lepromatous leprosy limb-girdle muscular dystrophy metachondromatosis microcystic adenoma microphthalmia mixed glioma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myositis ossificans myxoid leiomyosarcoma neuroendocrine carcinoma obsolete Matthew-Wood syndrome obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy osteoarthritis osteoporosis osteosarcoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenoma periostitis peritoneal carcinoma proliferative diabetic retinopathy prostate cancer prostate carcinoma pulmonary embolism pyelitis pyelonephritis rheumatoid arthritis rippling muscle disease 2 secondary Parkinson disease secondary hypertrophic osteoarthropathy severe nonproliferative diabetic retinopathy stone in bladder diverticulum thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma tracheal disease ulcerative colitis
32162	furrowed	fw	Drosophila melanogaster (fruit fly)	COVID-19 schizophrenia
16177	interleukin 1 receptor, type I	Il1r1	Mus musculus (house mouse)	COVID-19 cholesteatoma of middle ear chronic recurrent multifocal osteomyelitis pulpitis severe acute respiratory syndrome systemic scleroderma type 1 diabetes mellitus
100497509	ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) gene 4	abo.4	Xenopus tropicalis (tropical clawed frog)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
447881	globoside alpha-1,3-N-acetylgalactosaminyltransferase 1, like 3	gbgt1l3	Danio rerio (zebrafish)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
100005704	globoside alpha-1,3-N-acetylgalactosaminyltransferase 1, like 9	gbgt1l9	Danio rerio (zebrafish)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
550054	ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) gene 1	abo.1	Xenopus tropicalis (tropical clawed frog)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
566487	globoside alpha-1,3-N-acetylgalactosaminyltransferase 1, like 2	gbgt1l2	Danio rerio (zebrafish)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
100301568	ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase	Abo	Rattus norvegicus (Norway rat)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
80908	ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase	Abo	Mus musculus (house mouse)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
549858	ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) gene 2	abo.2	Xenopus tropicalis (tropical clawed frog)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
65270	histo-blood group ABO system transferase 3	Abo3	Rattus norvegicus (Norway rat)	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome

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