GlyCosmos Portal

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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 **876 - 900** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
390243	IZUMO1 receptor, JUNO	IZUMO1R Aliases: Folbp3 JUNO	Homo sapiens (human)	cancer
1594	cytochrome P450 family 27 subfamily B member 1	CYP27B1 Aliases: 1alpha(OH)ase 25-Hydroxyvitamin D3 1alpha-hydroxylase CYP1 Calcidiol 1-monooxygenase P450c1 VDDR I	Homo sapiens (human)	Addison's disease B-cell lymphoma Behcet's disease Crohn's colitis Crohn's disease Ehlers-Danlos syndrome Graves' disease Langerhans-cell histiocytosis Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wilson disease X-linked dominant hypophosphatemic rickets achondroplasia acquired immunodeficiency syndrome acute kidney failure adenocarcinoma adenoma adenosarcoma adrenal cortical hypofunction agnosia allergic asthma alopecia androgenic alopecia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis bacterial infectious disease basal cell carcinoma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cardiomyopathy central nervous system cancer cerebrotendinous xanthomatosis childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma chronic fatigue syndrome chronic granulomatous disease chronic kidney disease ciliary body disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency congestive heart failure coronary artery disease cribriform carcinoma dental enamel hypoplasia dermatitis developmental coordination disorder diabetes mellitus diabetic ketoacidosis diastolic heart failure differentiated thyroid gland carcinoma dysgerminoma dysplastic nevus syndrome embryoma encephalitis encephalomyelitis endomyocardial fibrosis essential hypertension exanthem gastroenteritis gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma hemochromatosis hepatitis B hepatitis C hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypercalcemia hyperphosphatemia hypertension hyperthyroidism hypertrophic cardiomyopathy hypoparathyroidism hypophosphatemia hypospadias idiopathic interstitial pneumonia ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intrinsic asthma iris disease iron metabolism disease kidney disease lactic acidosis large intestine cancer liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lymphoma melanoma mixed glioma multiple sclerosis myelitis nephritis nephroblastoma nephrocalcinosis nephrosis neuromyelitis optica non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ocular melanoma osteochondrodysplasia osteogenesis imperfecta osteomalacia osteoporosis osteosarcoma ovarian cancer ovarian carcinoma panuveitis papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis parathyroid adenoma parathyroid carcinoma phimosis phosphorus metabolism disease postinflammatory pulmonary fibrosis pre-eclampsia prostate cancer prostate carcinoma pseudohypoparathyroidism psoriasis psoriatic arthritis psychotic disorder pulmonary fibrosis pustulosis of palm and sole pyoureter renal carcinoma renal cell carcinoma reticulosarcoma retinoblastoma rickets sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophreniform disorder secondary hyperparathyroidism skin benign neoplasm skin cancer skin carcinoma skin melanoma squamous cell carcinoma steatotic liver disease thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma 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 ulcerative colitis urinary bladder cancer uveitis uveoparotid fever vitamin D-dependent rickets type 1A
161198	C-type lectin domain containing 14A	CLEC14A	Homo sapiens (human)	IgA glomerulonephritis breast cancer cancer embryoma lung adenocarcinoma lung cancer melanoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma skin melanoma thymic carcinoma thymoma
2023	enolase 1	ENO1 Aliases: MBP-1 PPH alpha-enolase	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 Behcet's disease Burkitt lymphoma Creutzfeldt-Jakob disease Duchenne muscular dystrophy EEC syndrome Fanconi anemia IgG4-related disease Lyme disease Pick's disease Reye syndrome Richter's syndrome acquired immunodeficiency syndrome acrodysostosis acute intermittent porphyria acute interstitial pneumonia acute myocardial infarction adenocarcinoma adenoma allergic asthma anemia anxiety disorder aphthous stomatitis arthritis arthropathy asthma atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune pancreatitis 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 bacterial infectious disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma blood coagulation disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cholangiocarcinoma cholera chromophobe renal cell carcinoma chronic kidney disease chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital heart disease congenital muscular dystrophy corneal disease coronary thrombosis cribriform carcinoma dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy distal arthrogryposis distal myopathy ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 embryoma endocarditis endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis esophageal cancer esophageal carcinoma essential hypertension exanthem eye disease facioscapulohumeral muscular dystrophy familial retinoblastoma fibromyalgia gastric adenocarcinoma generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemorrhoid hepatitis B hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hyperglycemia hypertension hypoglycemia idiopathic interstitial pneumonia immune system disease infective endocarditis inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal volvulus intrahepatic cholangiocarcinoma intrinsic asthma invasive ductal carcinoma keratoconus kidney disease large intestine cancer leiomyoma limb-girdle muscular dystrophy liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung squamous cell carcinoma lupus nephritis macrocytic anemia male infertility membranous glomerulonephritis microphthalmia middle cerebral artery infarction mixed glioma multiple myeloma multiple sclerosis muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myofibroma nasopharynx carcinoma nephritis nephrolithiasis nephrosis neuroblastoma nonpapillary renal cell 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 obsolete inherited blood coagulation disease oculopharyngeal muscular dystrophy oral submucous fibrosis osteoarthritis osteoporosis pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma patent ductus arteriosus perinatal necrotizing enterocolitis periodontitis phobic disorder primary pulmonary hypertension prostate cancer prostate carcinoma pulmonary hypertension pyoureter reflex sympathetic dystrophy renal carcinoma renal cell carcinoma retinoblastoma rheumatoid arthritis rippling muscle disease 2 sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction spondyloarthropathy spondylosis squamous cell carcinoma stomach cancer stomach carcinoma subacute bacterial endocarditis substance abuse substance-related disorder systemic lupus erythematosus tongue squamous cell carcinoma trilateral retinoblastoma tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uric acid nephrolithiasis urinary bladder cancer uterine corpus cancer uterine fibroid vasculitis
83639	testis expressed 101	TEX101 Aliases: CT131 MGC4766 SGRG SPATA44 TES101-reactive protein TES101RP cancer/testis antigen 131 spermatogenesis associated 44	Homo sapiens (human)	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 adenocarcinoma adenoma azoospermia basal cell carcinoma breast cancer breast ductal carcinoma cancer cribriform carcinoma embryoma granular cell carcinoma hepatocellular carcinoma liver cancer oligospermia tubular adenocarcinoma
5050	platelet activating factor acetylhydrolase 1b catalytic subunit 3	PAFAH1B3 Aliases: PAF-AH1b alpha 1 subunit	Homo sapiens (human)	intellectual disability learning disability
5095	propionyl-CoA carboxylase subunit alpha	PCCA	Homo sapiens (human)	Laron syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis amino acid metabolic disorder anemia cardiomyopathy cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dystonia endomyocardial fibrosis epilepsy granular cell carcinoma hypertrophic cardiomyopathy hypoglycemia intellectual disability lactic acidosis large intestine cancer learning disability macrocytic anemia neutropenia nicotine dependence obsolete constipation osteoporosis pancreatitis pancytopenia pontocerebellar hypoplasia type 2D propionic acidemia psoriatic arthritis refractive error severe congenital neutropenia sick sinus syndrome stomach cancer stomach carcinoma thrombocytopenia tubular adenocarcinoma urea cycle disorder visual epilepsy
3633	inositol polyphosphate-5-phosphatase B	INPP5B Aliases: type II inositol 1,4,5-trisphosphate 5-phosphatase	Homo sapiens (human)	Dent disease Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome amyotrophic lateral sclerosis 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 congenital hypothyroidism congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy giant cell glioblastoma glaucoma glioblastoma hypothyroidism limb-girdle muscular dystrophy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myxedema 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 progressive muscular atrophy rippling muscle disease 2
375790	agrin	AGRN	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 Bell's palsy Pick's disease Reye syndrome acute myeloid leukemia agnosia cancer central sleep apnea cerebral degeneration congenital myasthenic syndrome 10 congenital myasthenic syndrome 8 congenital myasthenic syndrome congenital nystagmus congenital ptosis critical illness polyneuropathy developmental coordination disorder dissociated nystagmus embryoma epilepsy esophagitis esotropia facial nerve disease facial paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gastroesophageal reflux disease intellectual disability learning disability lung adenocarcinoma lung cancer monocular esotropia obstructive sleep apnea ophthalmoplegia papillary adenocarcinoma papillary renal cell carcinoma pathologic nystagmus peptic esophagitis polyhydramnios polyneuropathy progressive bulbar palsy ptosis scoliosis sensorineural hearing loss spontaneous ocular nystagmus thyroid gland papillary carcinoma visual epilepsy
8396	phosphatidylinositol-5-phosphate 4-kinase type 2 beta	PIP4K2B Aliases: PIP5KIIB PIP5KIIbeta	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer embryoma pancreatic cancer pancreatic carcinoma
8876	vanin 1	VNN1 Aliases: Tiff66 pantetheinase pantetheine hydrolase	Homo sapiens (human)	B-cell lymphoma Evans' syndrome Fanconi syndrome allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis autoimmune thrombocytopenic purpura cancer cardiovascular system disease celiac disease chronic kidney disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease cystinosis disease of metabolism embryoma essential hypertension gastroenteritis heart disease hydronephrosis hypertension ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma large intestine cancer malaria obsolete ymphosarcoma obstructive nephropathy pancreatic ductal adenocarcinoma parapsoriasis psoriasis pustulosis of palm and sole renal osteodystrophy spondyloepimetaphyseal dysplasia, Sponastrime type steatotic liver disease ulcerative colitis ureteral obstruction
10232	mesothelin	MSLN Aliases: CAK1 MPF	Homo sapiens (human)	acoustic neuroma adenocarcinoma adenoma adenosarcoma adult acute lymphocytic leukemia angiomatous meningioma anthracosilicosis asbestosis benign meningioma benign mesothelioma bile duct adenocarcinoma bile duct cancer bile duct carcinoma breast cancer bronchus cancer bronchus carcinoma byssinosis cancer carcinoma cerebral convexity meningioma cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervicitis cervix carcinoma childhood leukemia cholangiocarcinoma chronic salpingo-oophoritis clear cell meningioma colorectal cancer colorectal carcinoma common bile duct neoplasm cribriform carcinoma distal arthrogryposis embryoma endocervicitis endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma essential hypertension fibrous meningioma gastric adenocarcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer hepatocellular carcinoma high grade glioma hypertension intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma kidney failure large intestine cancer liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma malignant mesothelioma malignant pleural mesothelioma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma nephroblastoma obsolete Matthew-Wood syndrome olfactory groove meningioma ovarian cancer ovarian carcinoma ovary serous adenocarcinoma pancreas disease pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma parasagittal meningioma patent ductus arteriosus pituitary adenoma psammomatous meningioma salivary gland cancer sarcomatoid carcinoma secretory meningioma spinal meningioma stomach cancer stomach carcinoma thymic carcinoma thymoma transitional meningioma tubular adenocarcinoma uterine corpus cancer
55304	serine palmitoyltransferase long chain base subunit 3	SPTLC3 Aliases: FLJ11112 LCB2B hLCB2b	Homo sapiens (human)	autosomal dominant cerebellar ataxia bacterial sepsis head and neck squamous cell carcinoma hereditary sensory and autonomic neuropathy type 1 neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy sensory peripheral neuropathy spinocerebellar ataxia type 7
35	acyl-CoA dehydrogenase short chain	ACADS Aliases: ACAD3 SCAD	Homo sapiens (human)	Bell's palsy Cockayne syndrome Cornelia de Lange syndrome Dubowitz 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 Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Stevens-Johnson syndrome X-linked Aarskog syndrome alcohol use disorder arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bipolar disorder cancer cardiomyopathy chondrodysplasia-pseudohermaphroditism syndrome chronic kidney disease congestive heart failure coronary artery disease embryoma endomyocardial fibrosis epilepsy erythema multiforme facial nerve disease facial paralysis familial periodic paralysis hepatocellular carcinoma hypertrophic cardiomyopathy liver cancer medium chain acyl-CoA dehydrogenase deficiency microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II myopathy nutmeg liver pancreatic cancer pancreatic carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder scoliosis short chain acyl-CoA dehydrogenase deficiency visual epilepsy
126	alcohol dehydrogenase 1C (class I), gamma polypeptide	ADH1C	Homo sapiens (human)	Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adrenoleukodystrophy adult hepatocellular carcinoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis anaplastic astrocytoma arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant hypocalcemia 1 autosomal dominant hypocalcemia bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiovascular system disease cerebellar ataxia, mental retardation and dysequlibrium syndrome cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood cerebral astrocytoma childhood hepatocellular carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart coronary artery disease coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis fibrillary astrocytoma follicular adenoma gallbladder disease gemistocytic astrocytoma glucose intolerance granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemorrhoid hepatocellular carcinoma high grade glioma islet cell tumor juvenile pilocytic astrocytoma large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer late onset Parkinson's disease liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder malignant astrocytoma melancholic depression microcystic adenoma myocardial infarction neurotic disorder nicotine dependence nutmeg liver obsolete constipation obsolete melancholia oropharynx cancer pancreatic cancer pancreatic carcinoma pancreatitis papillary adenoma pharynx cancer pilocytic astrocytoma prediabetes syndrome prostate cancer prostate carcinoma protoplasmic astrocytoma secondary Parkinson disease silent myocardial infarction situs inversus squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tongue squamous cell carcinoma tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer
8985	procollagen-lysine,2-oxoglutarate 5-dioxygenase 3	PLOD3 Aliases: LH3 Multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3 lysyl hydroxlase 3	Homo sapiens (human)	bone disease bronchus cancer bronchus carcinoma cancer cartilage disease cataract central nervous system cancer central nervous system lymphoma clubfoot collagen disease congenital hypothyroidism connective tissue disease diaphragmatic eventration embryoma epidermolysis bullosa simplex Dowling-Meara type epidermolysis bullosa simplex Ogna type epidermolysis bullosa simplex with muscular dystrophy epidermolysis bullosa simplex epidermolysis bullosa esophageal cancer esophageal carcinoma gamma-glutamyl transpeptidase deficiency giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma hypothyroidism liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoma mixed glioma myopia myxedema nonsyndromic congenital nail disorder 9 obsolete ymphosarcoma placental insufficiency scoliosis sensorineural hearing loss thoracic aortic aneurysm
8473	O-linked N-acetylglucosamine (GlcNAc) transferase	OGT Aliases: FLJ23071 HRNT1 MGC22921 O-GLCNAC OGT1 UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase	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 Zollinger-Ellison syndrome amblyopia aortic valve disease 2 aortic valve stenosis autoimmune hepatitis breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration chromophobe renal cell carcinoma chronic ulcer of skin clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congenital nystagmus congestive heart failure cryptorchidism diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma dissociated nystagmus embryoma heart disease hepatitis C hepatocellular carcinoma hyperinsulinism hypospadias intellectual disability large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver cancer liver carcinoma liver cirrhosis microcephaly microphthalmia myoepithelioma neurodegenerative disease non-syndromic X-linked intellectual disability 106 nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma pathologic nystagmus renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma spontaneous ocular nystagmus steatotic liver disease stomach cancer stomach carcinoma strabismic amblyopia tauopathy type 2 diabetes mellitus
477	ATPase Na+/K+ transporting subunit alpha 2	ATP1A2	Homo sapiens (human)	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
6518	solute carrier family 2 member 5	SLC2A5	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 acute myeloid leukemia breast cancer breast carcinoma cancer central nervous system cancer childhood B-cell acute lymphoblastic leukemia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetes mellitus disease of metabolism embryoma essential hypertension gliosarcoma hepatocellular carcinoma high grade glioma hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease intestinal atresia large intestine cancer liver cancer long QT syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung non-small cell carcinoma mixed glioma neuroblastoma nonpapillary renal cell carcinoma obesity ovarian cancer ovarian carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma seminoma testicular cancer testicular germ cell cancer testis seminoma tropical sprue type 2 diabetes mellitus
6185	ribophorin II	RPN2 Aliases: RIBIIR RPN-II RPNII SWP1 oligosaccharyltransferase complex subunit (non-catalytic)	Homo sapiens (human)	bipolar disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer colon carcinoma colorectal cancer colorectal carcinoma diabetes mellitus embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma nasopharynx carcinoma prostate cancer prostate carcinoma schizoaffective disorder schizophrenia schizophreniform disorder stomach cancer stomach carcinoma type 2 diabetes mellitus
5311	polycystin 2, transient receptor potential cation channel	PKD2 Aliases: PC2 PKD4 Pc-2 TRPP2 transient receptor potential cation channel, subfamily P, member 2	Homo sapiens (human)	Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome Wiskott-Aldrich syndrome acute kidney failure adrenal gland cancer atrial fibrillation atrioventricular block autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone disease breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebellar ataxia, mental retardation and dysequlibrium syndrome cholangiocarcinoma chronic kidney disease ciliopathy collagen disease congenital heart disease congestive heart failure connective tissue disease cystic kidney disease disorder of sexual development distal arthrogryposis duodenum cancer embryoma episodic kinesigenic dyskinesia 1 essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis focal segmental glomerulosclerosis giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis gout heart cancer hermaphroditism high grade glioma hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intracranial aneurysm intrahepatic cholangiocarcinoma islet cell tumor kidney disease kidney failure laryngeal squamous cell carcinoma lung adenocarcinoma lung cancer mixed glioma nephritis nephrosis neurodegenerative disease non-congenital cyst of kidney pheochromocytoma placental insufficiency polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 4 polycystic kidney disease polycystic liver disease prostate cancer prostate carcinoma pseudohermaphroditism pyoureter retinal degeneration situs inversus small intestine cancer thoracic aortic aneurysm tuberous sclerosis uremia urinary bladder cancer
2539	glucose-6-phosphate dehydrogenase	G6PD Aliases: G6PD1	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 B-cell lymphoma Baraitser-Winter syndrome Bartter disease Bloch-Sulzberger syndrome Burkitt lymphoma Chagas disease Conn's syndrome Creutzfeldt-Jakob disease Duchenne muscular dystrophy Emery-Dreifuss muscular dystrophy Fabry disease Fraser syndrome Gilbert syndrome Goldenhar syndrome IGSF1 deficiency syndrome Japanese encephalitis Langerhans-cell histiocytosis Moebius syndrome Muenke Syndrome Nance-Horan syndrome Native American myopathy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Plasmodium ovale malaria Plasmodium vivax malaria Renpenning syndrome Reye syndrome Richter's syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Waterhouse-Friderichsen syndrome Weissenbacher-Zweymuller syndrome Werner syndrome Wilson disease Wiskott-Aldrich syndrome X-linked chronic granulomatous disease abdominal obesity-metabolic syndrome 1 achromatopsia acoustic neuroma acquired color blindness acquired immunodeficiency syndrome acquired polycythemia acute chest syndrome acute kidney failure acute lymphoblastic leukemia acute megakaryocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal cortex cancer adrenal gland cancer adrenoleukodystrophy adult acute lymphocytic leukemia adult hepatocellular carcinoma adult lymphoma age related macular degeneration allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia amyloidosis anaplastic astrocytoma anemia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anogenital venereal wart asthma ataxia telangiectasia atypical chronic myeloid leukemia, BCR-ABL1 negative atypical hemolytic-uremic syndrome autistic disorder bacterial sepsis beta thalassemia bilirubin metabolic disorder bipolar disorder bladder carcinoma blastomycosis blood group incompatibility blue color blindness bone marrow cancer borderline personality disorder brain cancer brain ischemia brain stem infarction branchiootic syndrome breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiomyopathy cardiovascular system disease cataract central nervous system cancer central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood hepatocellular carcinoma childhood leukemia childhood lymphoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chromophobe renal cell carcinoma chronic granulomatous disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chylomicron retention disease classic galactosemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma common cold common wart conduct disorder cone-rod dystrophy congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia congenital hemolytic anemia congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nonspherocytic hemolytic anemia congestive heart failure contact dermatitis coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma cutaneous leishmaniasis cystinuria degeneration of macula and posterior pole dementia dengue disease dengue hemorrhagic fever diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism duodenum cancer embryoma endocarditis endomyocardial fibrosis epilepsy epithelioid malignant peripheral nerve sheath tumor erythropoietin polycythemia esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia factor VIII deficiency familial adenomatous polyposis 1 familial adenomatous polyposis familial erythrocytosis 2 familial hyperlipidemia familial periodic paralysis favism fetal erythroblastosis fibrillary astrocytoma fragile X syndrome fundus albipunctatus galactokinase deficiency galactosemia gemistocytic astrocytoma gliosarcoma glomerulonephritis glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart cancer heart disease hematologic cancer hematopoietic system disease hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobin H disease hemoglobinopathy hemoglobinuria hemolytic anemia hemolytic-uremic syndrome hemophilia B hepatic coma hepatic encephalopathy hepatitis A hepatitis B hepatitis hepatoblastoma hepatocellular carcinoma hereditary elliptocytosis hereditary spherocytosis hidradenoma high grade glioma human immunodeficiency virus infectious disease hyperhomocysteinemia hyperparathyroidism hypertension hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia hypomelanosis of Ito hypothyroidism inherited metabolic disorder intellectual disability intermittent explosive disorder intrinsic asthma iron metabolism disease juvenile pilocytic astrocytoma kernicterus due to isoimmunization kernicterus kidney cancer kidney disease large intestine cancer learning disability leishmaniasis leukemia lingual-facial-buccal dyskinesia lipid storage disease liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macrocytic anemia macular degeneration malaria malignant astrocytoma malignant peripheral nerve sheath tumor melanoma metabolic dysfunction-associated steatotic liver disease methemoglobinemia middle cerebral artery infarction mixed glioma movement disease mucocutaneous leishmaniasis multiple myeloma muscular dystrophy myelodysplastic syndrome myelofibrosis myeloid leukemia myeloproliferative neoplasm myocardial infarction myopathy myxedema neonatal jaundice nephritis nephrogenic diabetes insipidus nephrosis neurilemmoma neuroblastoma neurodegenerative disease neurofibromatosis 1 neurofibromatosis neurofibrosarcoma non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete subacute myeloid leukemia obsolete ymphosarcoma occupational dermatitis oculocerebrorenal syndrome orofaciodigital syndrome I orofaciodigital syndrome X osteitis fibrosa pancytopenia papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis parathyroid adenoma parathyroid carcinoma paroxysmal nocturnal hemoglobinuria peroxisome biogenesis disorder 8A phagocyte bactericidal dysfunction phenylketonuria pheochromocytoma pilocytic astrocytoma plasmacytoma pneumocystosis polycythemia vera polycythemia prediabetes syndrome priapism primary hyperaldosteronism primary immunodeficiency disease primary pulmonary hypertension progeria prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder pterygium pyoureter pyruvate kinase deficiency of red cells red color blindness red-green color blindness renal carcinoma renal cell carcinoma renovascular hypertension reticulosarcoma retinitis pigmentosa rhabdomyosarcoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder senile cataract sickle cell anemia silent myocardial infarction skin melanoma skin papilloma skin tag small intestine cancer spondylocarpotarsal synostosis syndrome steatotic liver disease stress polycythemia subependymal giant cell astrocytoma sulfhemoglobinemia syringoma thalassemia thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma transient cerebral ischemia trypanosomiasis tubular adenocarcinoma 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 urinary bladder cancer vascular dementia vascular disease vertebrobasilar insufficiency viral infectious disease visceral leishmaniasis visual epilepsy vitiligo yellow fever
3036	hyaluronan synthase 1	HAS1	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 Richter's syndrome adenocarcinoma adenoma arthritis arthropathy basal cell carcinoma bladder carcinoma breast cancer breast carcinoma cancer carcinoma cerebral degeneration chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma cribriform carcinoma embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis gallbladder disease granular cell carcinoma hepatitis A hepatitis hepatocellular carcinoma liver cancer liver disease lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance monoclonal paraproteinemia multiple myeloma nonpapillary renal cell carcinoma obsolete lymphoplasmacytic lymphoma osteoarthritis papillary renal cell carcinoma peritoneal mesothelioma plasma cell neoplasm polycystic ovary syndrome primary pulmonary hypertension pulmonary hypertension renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma sebaceous carcinoma stomach cancer stomach carcinoma sweat gland cancer tubular adenocarcinoma urinary bladder cancer
5506	protein phosphatase 1 regulatory subunit 3A	PPP1R3A Aliases: GM glycogen-associated regulatory subunit of protein phosphatase-1 protein phosphatase 1 regulatory subunit GM	Homo sapiens (human)	Alzheimer's disease adult lymphoma atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative breast cancer cancer carcinoma central nervous system lymphoma childhood lymphoma chronic monocytic leukemia colorectal cancer colorectal carcinoma communication disorder congestive heart failure diabetes mellitus diabetic ketoacidosis embryoma glucose intolerance hematologic cancer hypoglycemia language disorder large intestine cancer laryngeal squamous cell carcinoma lymphoid leukemia lymphoma myeloid leukemia obsolete ymphosarcoma prediabetes syndrome prostate cancer prostate carcinoma sarcomatoid carcinoma type 2 diabetes mellitus
254773	lysozyme g2	LYG2 Aliases: LYGA2 LYGH	Homo sapiens (human)

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