GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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 **826 - 850** of **1582** in total

« First

‹ Prev

…

30

31

32

33

34

35

36

37

38

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
5277	phosphatidylinositol glycan anchor biosynthesis class A	PIGA Aliases: GPI3 GPI3 (SPT14) homolog (S. cerevisiae) PIG-A Phosphatidylinositol N-acetylglucosaminyltransferase subunit A paroxysmal nocturnal hemoglobinuria	Homo sapiens (human)	Barrett's esophagus Burkitt lymphoma Hirschsprung's disease Marfan syndrome Miller-Dieker lissencephaly syndrome Simpson-Golabi-Behmel syndrome type 1 Simpson-Golabi-Behmel syndrome type 2 Unverricht-Lundborg syndrome West syndrome acute myeloid leukemia acute myocardial infarction antithrombin III deficiency aplastic anemia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atypical hemolytic-uremic syndrome autoimmune disease autoimmune lymphoproliferative syndrome autosomal recessive congenital ichthyosis 4B blepharospasm blood coagulation disease bone marrow cancer brain disease cancer chondroma chromosome 17p13.1 deletion syndrome coronary thrombosis dental caries dentin caries developmental and epileptic encephalopathy 3 early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy esophagitis esophagus adenocarcinoma essential thrombocythemia extramedullary plasmacytoma fetal erythroblastosis focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth hematopoietic system disease hemoglobinuria hemolytic anemia hemolytic-uremic syndrome immune system disease inflammatory bowel disease intellectual disability learning disability lissencephaly multiple congenital anomalies-hypotonia-seizures syndrome 2 multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction obsolete congenital ichthyosiform erythroderma obsolete infantile epileptic encephalopathy paroxysmal nocturnal hemoglobinuria patent foramen ovale peptic esophagitis plasma cell neoplasm plasmacytoma polycythemia vera primary pulmonary hypertension protein C deficiency protein S deficiency pulmonary embolism sensorineural hearing loss silent myocardial infarction situs inversus thrombophilia thrombotic thrombocytopenic purpura transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis vertebrobasilar insufficiency visual epilepsy
221823	phosphoribosyl pyrophosphate synthetase 1 like 1	PRPS1L1 Aliases: PRPS3	Homo sapiens (human)
27235	coenzyme Q2, polyprenyltransferase	COQ2	Homo sapiens (human)	coenzyme Q10 deficiency disease glucose intolerance multiple system atrophy nephrotic syndrome primary coenzyme Q10 deficiency 1
9917	FAM20B glycosaminoglycan xylosylkinase	FAM20B Aliases: GXK1 KIAA0475	Homo sapiens (human)	Desbuquois dysplasia Ehlers-Danlos syndrome osteogenesis imperfecta parapsoriasis psoriasis pustulosis of palm and sole
54898	ELOVL fatty acid elongase 2	ELOVL2 Aliases: Ssc2	Homo sapiens (human)	acute chest syndrome acute myocardial infarction autism spectrum disorder autistic disorder central nervous system cancer coronary artery disease coronary thrombosis giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma liver cancer melanoma mixed glioma myocardial infarction papillary adenocarcinoma papillary renal cell carcinoma silent myocardial infarction skin melanoma steatotic liver disease thyroid gland papillary carcinoma
2876	glutathione peroxidase 1	GPX1 Aliases: selenoprotein GPX1	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 Bannayan-Riley-Ruvalcaba syndrome Barrett's esophagus Cowden syndrome Crohn's colitis Crohn's disease Down syndrome Friedreich ataxia 1 Friedreich ataxia Graves' disease Huntington's disease Keshan disease Klebsiella pneumonia Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Wilson disease X-linked dilated cardiomyopathy Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acquired immunodeficiency syndrome acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adamantinous craniopharyngioma adenocarcinoma adenoma adult lymphoma agnosia alcoholic liver cirrhosis allergic asthma alpha thalassemia alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis type 1 anemia angioedema angiomatous meningioma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autistic disorder autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autonomic neuropathy benign meningioma bladder carcinoma bone disease bone giant cell tumor bone marrow cancer brain ischemia breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis cancer cardiovascular system disease cartilage disease cataract central nervous system cancer central nervous system disease central nervous system lymphoma cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood lymphoma cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism connective tissue disease corneal disease coronary artery disease coronary thrombosis craniopharyngioma cribriform carcinoma critical illness polyneuropathy cutaneous mastocytosis dementia depressive disorder diabetes mellitus diabetic angiopathy diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diffuse cutaneous mastocytosis diffuse large B-cell lymphoma 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 dysthymic disorder dystonia embryoma epilepsy essential hypertension familial mediterranean fever fibromyalgia fibrous meningioma follicular adenoma follicular lymphoma gastric adenocarcinoma gastric ulcer gastroenteritis gestational diabetes gliosarcoma glucocorticoid-remediable aldosteronism granular cell carcinoma hairy cell leukemia head and neck cancer head and neck squamous cell carcinoma heart disease hemiplegia hemochromatosis hepatitis C hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hyperglycemia hyperhomocysteinemia hyperinsulinism hypertension hyperthyroidism hypothyroidism ileitis ileocolitis immune system disease inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intermittent claudication intestinal benign neoplasm intestinal cancer intraorbital meningioma intraventricular meningioma intrinsic asthma iron deficiency anemia iron metabolism disease keratoconus kidney cancer large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer leukemia lingual-facial-buccal dyskinesia liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung squamous cell carcinoma lymphoma lymphoplasmacyte-rich meningioma macrocytic anemia major depressive disorder malaria mastocytosis melancholic depression melanoma meningioma meningoencephalitis meningothelial meningioma mevalonic aciduria microcystic adenoma microcystic meningioma microphthalmia mitochondrial metabolism disease mitochondrial myopathy mixed glioma morbid obesity multiple myeloma myeloid neoplasm myeloproliferative neoplasm myocardial infarction myocarditis myxedema nasopharynx carcinoma neonatal jaundice nephrolithiasis nephrosis nephrotic syndrome nervous system disease neuroblastoma neuropathy neurotic disorder non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma olfactory groove meningioma osteoarthritis osteoporosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panic disorder papillary adenoma papillary craniopharyngioma papillary renal cell carcinoma parapsoriasis parasagittal meningioma periodontitis peripheral nervous system disease peripheral vascular disease pituitary adenoma placental insufficiency pneumocystosis pneumonia poikiloderma with neutropenia polycystic ovary syndrome polyneuropathy post-traumatic stress disorder pre-eclampsia prostate cancer prostate carcinoma prostate disease psammomatous meningioma pseudoxanthoma elasticum psoriasis pulmonary emphysema pustulosis of palm and sole reflex sympathetic dystrophy renal carcinoma renal cell carcinoma renal osteodystrophy reticulosarcoma retrograde amnesia rheumatoid arthritis sarcomatoid renal cell carcinoma schizophrenia secretory meningioma senile cataract sickle cell anemia silent myocardial infarction skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal meningioma squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis substance abuse substance-related disorder superficial urinary bladder cancer thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyrotoxicosis tongue squamous cell carcinoma tonsillitis transient cerebral ischemia transitional cell carcinoma transitional meningioma 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 uric acid nephrolithiasis urinary bladder cancer urticaria pigmentosa urticaria vascular dementia vitiligo
51302	cytochrome P450 family 39 subfamily A member 1	CYP39A1	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome agranulocytosis gallbladder cancer gallbladder carcinoma hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia leukopenia liver cancer neutropenia prostate cancer prostate carcinoma severe congenital neutropenia
6713	squalene epoxidase	SQLE Aliases: squalene monooxygenase	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 breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration colorectal cancer colorectal carcinoma embryoma esophagus squamous cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer long QT syndrome lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma microphthalmia neuroendocrine carcinoma neuroendocrine tumor obsolete Matthew-Wood syndrome prostate cancer prostate carcinoma sick sinus syndrome steatotic liver disease tinea corporis
84725	pleckstrin homology domain containing A8	PLEKHA8 Aliases: FAPP2 MGC3358	Homo sapiens (human)	breast cancer breast carcinoma cancer central nervous system cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer embryoma gliosarcoma high grade glioma large intestine cancer mixed glioma
10005	acyl-CoA thioesterase 8	ACOT8 Aliases: NAP1 Nef (lentivirus myristoylated factor) associated protein 1 PTE-2 choloyl-CoA hydrolase hACTE-III hTE	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 Thiel-Behnke corneal dystrophy acquired immunodeficiency syndrome bacterial sepsis cancer cerebral degeneration diabetes insipidus diarrhea embryoma hepatocellular carcinoma human immunodeficiency virus infectious disease hypophosphatemia liver cancer low tension glaucoma lung cancer lung non-small cell carcinoma neurohypophyseal diabetes insipidus parapsoriasis psoriasis pustulosis of palm and sole
140838	N-acetylneuraminic acid phosphatase	NANP Aliases: MGC26833 dJ694B14.3	Homo sapiens (human)	cancer cerebral degeneration colorectal cancer esophageal cancer esophageal carcinoma large intestine cancer malaria
2026	enolase 2	ENO2 Aliases: NSE gamma-enolase neuron specific enolase neuronal enriched 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 Creutzfeldt-Jakob disease Down syndrome Ewing sarcoma Gilbert syndrome Gilles de la Tourette syndrome Guillain-Barre syndrome Hirschsprung's disease IGSF1 deficiency syndrome Leber congenital amaurosis Leber hereditary optic neuropathy Lewy body dementia Lyme disease Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Parkinsonism Pick's disease Rett syndrome Reye syndrome Sveinsson chorioretinal atrophy T-cell acute lymphoblastic leukemia abdominal obesity-metabolic syndrome 1 acoustic neuroma acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult lymphoma adult oligodendroglioma allergic asthma alternating hemiplegia of childhood angiomatous meningioma anorectal stricture aseptic meningitis asphyxia neonatorum asthma atrial fibrillation autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy bacterial meningitis bacterial sepsis benign meningioma bilirubin metabolic disorder bladder carcinoma bladder urothelial carcinoma brain cancer brain disease brain ischemia brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest central nervous system disease central nervous system lymphoma cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia childhood lymphoma childhood oligodendroglioma chromophobe renal cell carcinoma chronic tic disorder clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma complex partial epilepsy congenital heart disease 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 congestive heart failure coronary thrombosis cribriform carcinoma depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diffuse large B-cell lymphoma embryoma encephalitis encephalomyelitis endometrial carcinoma epilepsy eye disease familial retinoblastoma fibrous meningioma focal epilepsy follicular adenoma giant cell glioblastoma glioblastoma glomerulonephritis glycogen storage disease IV glycogen storage disease VI glycogen storage disease VII granular cell carcinoma heroin dependence high grade glioma hyperglycemia hypertension hypoglycemia hypothyroidism immune system disease impotence intracranial hypertension intraorbital meningioma intraventricular meningioma intrinsic asthma kidney disease leukemia lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphoblastic lymphoma lymphoma major depressive disorder malaria malignant teratoma medulloblastoma medulloepithelioma melancholic depression melanoma meningioma meningoencephalitis meningothelial meningioma microcystic adenoma microcystic meningioma migraine without aura mixed oligodendroglioma-astrocytoma morphine dependence myelitis myeloproliferative disorder with eosinophilia myocardial infarction myxedema nephritis nephroblastoma nephrosis nervous system cancer nervous system disease neuroblastoma neurodegeneration with brain iron accumulation 5 neurodegenerative disease neuroectodermal tumor neuroendocrine carcinoma neuroendocrine tumor neurofibromatosis 1 neurofibromatosis neuropathy neurotic disorder nodular prostate nonpapillary renal cell carcinoma obesity obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma olfactory groove meningioma oligodendroglioma opiate dependence optic atrophy optic papillitis ossifying fibromyxoid tumor papillary adenoma papillary carcinoma papillary renal cell carcinoma papilledema paraganglioma parasagittal meningioma partial motor epilepsy peripheral nervous system disease pineal gland cancer pineoblastoma pituitary adenoma polyneuropathy premature ejaculation primary cutaneous amyloidosis proliferative diabetic retinopathy prostate cancer prostate carcinoma prostatic adenoma psammomatous meningioma pseudotumor cerebri psychologic dyspareunia pulmonary alveolar proteinosis pulmonary large cell neuroendocrine carcinoma pulmonary tuberculosis pyoureter renal carcinoma renal cell carcinoma retinal edema retinoblastoma rhabdomyosarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia secondary Parkinson disease secretory meningioma silent myocardial infarction skin melanoma spinal meningioma squamous cell carcinoma squamous cell neoplasm steatotic liver disease subacute delirium supratentorial primitive neuroectodermal tumor synovial sarcoma temporal lobe epilepsy teratoma tic disorder tick-borne encephalitis tongue squamous cell carcinoma toxic shock syndrome transient tic disorder transitional meningioma trilateral retinoblastoma tuberculosis tuberculous pneumothorax 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 disease viral meningitis visual epilepsy
55508	solute carrier family 35 member E3	SLC35E3 Aliases: BLOV1	Homo sapiens (human)	cardiovascular system disease heart disease
5105	phosphoenolpyruvate carboxykinase 1	PCK1 Aliases: PEPCK-C	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 abdominal obesity-metabolic syndrome 1 biliary atresia cancer celiac disease cerebral degeneration colorectal cancer colorectal carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congestive heart failure cryptococcosis cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma epilepsy gestational diabetes hepatic coma hepatic encephalopathy hepatocellular carcinoma hyperglycemia hypoglycemia lactic acidosis large intestine cancer leprosy lipoatrophic diabetes mellitus lipodystrophy liver cancer liver carcinoma maturity-onset diabetes of the young metabolic dysfunction-associated steatohepatitis multiple sclerosis obesity optic atrophy placental insufficiency pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency schizophrenia steatotic liver disease type 2 diabetes mellitus visual epilepsy
127	alcohol dehydrogenase 4 (class II), pi polypeptide	ADH4 Aliases: ADH-2	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute myeloid leukemia acute pancreatitis adenocarcinoma adenoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis anaplastic astrocytoma cancer carcinoma childhood cerebral astrocytoma cribriform carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fibrillary astrocytoma flat ductal epithelial atypia gemistocytic astrocytoma granular cell carcinoma hepatitis C hepatocellular carcinoma high grade glioma invasive ductal carcinoma juvenile pilocytic astrocytoma liver cancer liver cirrhosis malignant astrocytoma migraine ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pharynx cancer pilocytic astrocytoma protoplasmic astrocytoma squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma
3988	lipase A, lysosomal acid type	LIPA Aliases: CESD LAL Wolman disease lysosomal acid lipase sterol esterase	Homo sapiens (human)	Addison's disease 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Balkan nephropathy Marfan syndrome Niemann-Pick disease type C1 Niemann-Pick disease Peyronie's disease Pick's disease Reye syndrome Wolman disease abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute chest syndrome acute lymphoblastic leukemia acute myocardial infarction adrenal cortical hypofunction adult acute lymphocytic leukemia allergic asthma anal carcinoma anal margin carcinoma anal margin squamous cell carcinoma anal squamous cell carcinoma anemia anus benign neoplasm anus cancer anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis balanitis xerotica obliterans cancer cardiac arrest cardiovascular system disease cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood B-cell acute lymphoblastic leukemia childhood acute lymphocytic leukemia cholestasis cholesterol ester storage disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diarrhea dysthymic disorder essential hypertension familial hypercholesterolemia familial hyperlipidemia gallbladder disease generalized anxiety disorder heart disease hepatitis B hepatitis C human immunodeficiency virus infectious disease hypertension intrinsic asthma karyomegalic interstitial nephritis kwashiorkor lipid storage disease liver cirrhosis liver disease lung squamous cell carcinoma lysosomal acid lipase deficiency lysosomal storage disease macrocytic anemia major depressive disorder marasmus melancholic depression melanoma myocardial infarction neurotic disorder nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete melancholia obsolete steatorrhea pancytopenia papillary renal cell carcinoma phobic disorder primary pulmonary hypertension prostate cancer prostate carcinoma protein-energy malnutrition renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction situs inversus skin melanoma squamous cell carcinoma steatotic liver disease tongue squamous cell carcinoma tuberous sclerosis type 2 diabetes mellitus
57511	component of oligomeric golgi complex 6	COG6 Aliases: COD2 KIAA1134	Homo sapiens (human)	Gilbert syndrome acquired hyperkeratosis allergic asthma anemia anhidrosis asthma bilirubin metabolic disorder blood coagulation disease cerebral degeneration cholestasis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIl congenital disorder of glycosylation coronary artery disease dental caries dental enamel hypoplasia dentin caries developmental and epileptic encephalopathy 36 epilepsy gastroenteritis gastrointestinal system disease hydrocephalus hypohidrosis intellectual disability intestinal disease intrinsic asthma juvenile rheumatoid arthritis learning disability leiomyoma macrocytic anemia microcephaly myofibroma nonepidermolytic palmoplantar keratoderma palmoplantar keratosis pancytopenia parapsoriasis placental insufficiency primary biliary cholangitis primary immunodeficiency disease proctitis psoriasis pustulosis of palm and sole rheumatoid arthritis systemic lupus erythematosus thrombocytopenia uterine fibroid visual epilepsy
144423	glycosyltransferase 1 domain containing 1	GLT1D1 Aliases: FLJ31978	Homo sapiens (human)	St. Louis encephalitis allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis coronary artery disease intrinsic asthma
55526	dehydrogenase E1 and transketolase domain containing 1	DHTKD1	Homo sapiens (human)	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
138429	phosphatidylinositol-4-phosphate 5-kinase like 1	PIP5KL1 Aliases: MGC46424 bA203J24.5	Homo sapiens (human)	cancer cervical cancer cervix carcinoma embryoma stomach cancer stomach carcinoma in situ stomach carcinoma
7124	tumor necrosis factor	TNF	Homo sapiens (human)	Alzheimer's disease Behcet's disease COVID-19 Cor pulmonale Crohn's disease Fanconi anemia Gaucher's disease Graves ophthalmopathy Graves' disease IgA glomerulonephritis Kawasaki disease Mycobacterium avium complex disease Mycoplasma pneumoniae pneumonia Plasmodium falciparum malaria Sjogren's syndrome Stevens-Johnson syndrome Vogt-Koyanagi-Harada disease Weill-Marchesani syndrome acne acquired immunodeficiency syndrome acute myocardial infarction adult respiratory distress syndrome alcoholic hepatitis amyloidosis anemia anogenital venereal wart anterior uveitis anti-basement membrane glomerulonephritis aortic valve stenosis aplastic anemia aspiration pneumonia asthma atopic dermatitis atrial fibrillation autistic disorder autoimmune hepatitis bacterial pneumonia beta thalassemia brain infarction breast adenocarcinoma breast cancer bronchiectasis bronchopulmonary dysplasia cardiac arrest cardiomyopathy cerebral infarction cervical cancer cholesteatoma of middle ear chorioamnionitis chronic obstructive pulmonary disease cicatricial pemphigoid cochlear disease congenital diaphragmatic hernia congestive heart failure corneal ulcer coronary artery disease coronary restenosis cryoglobulinemia cutaneous leishmaniasis cystic fibrosis cystitis dermatitis herpetiformis dermatitis diabetic angiopathy diabetic neuropathy diabetic retinopathy dilated cardiomyopathy 1H dilated cardiomyopathy disseminated intravascular coagulation encephalitis end stage renal disease endometriosis endophthalmitis epididymitis epilepsy erythema nodosum esophagitis extrinsic allergic alveolitis eye disease farmer's lung gastritis glaucoma heart valve disease hemochromatosis hepatitis A hepatitis B hepatocellular carcinoma hepatopulmonary syndrome hepatorenal syndrome hereditary hemorrhagic telangiectasia herpes zoster hidradenitis suppurativa high grade glioma human immunodeficiency virus infectious disease hypertension hypochromic microcytic anemia impotence inclusion body myopathy with Paget disease of bone and frontotemporal dementia inflammatory bowel disease intermediate uveitis intracranial aneurysm iron deficiency anemia keratoconjunctivitis sicca kidney disease leprosy liver cirrhosis liver disease low tension glaucoma lung disease lung non-small cell carcinoma lupus nephritis lymphopenia malaria metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease mevalonic aciduria middle cerebral artery infarction migraine without aura migraine mixed connective tissue disease mucocutaneous leishmaniasis mucopolysaccharidosis VI multiple myeloma multiple sclerosis muscular dystrophy myelodysplastic syndrome myocardial infarction myositis neutropenia obesity obstructive sleep apnea open-angle glaucoma oral squamous cell carcinoma otitis media ovarian cancer paracoccidioidomycosis peptic esophagitis perinatal necrotizing enterocolitis periodontitis peritonitis periventricular leukomalacia pleurisy portal hypertension pre-eclampsia primary biliary cholangitis primary open angle glaucoma primary sclerosing cholangitis prostate cancer psoriasis psoriatic arthritis pulmonary edema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis pulmonary tuberculosis pustulosis of palm and sole radiculopathy renal cell carcinoma renal hypertension retinal detachment rheumatoid arthritis rhinitis root resorption schizophrenia sciatic neuropathy scleritis sensorineural hearing loss severe acute respiratory syndrome sickle cell anemia silicosis skin disease small cell carcinoma spondyloarthropathy status epilepticus systemic lupus erythematosus thalassemia thrombocytopenia toxic shock syndrome trachoma transient cerebral ischemia tuberculosis type 1 diabetes mellitus type 2 diabetes mellitus typhoid fever ulcerative colitis ureteral obstruction uveitis vascular dementia visceral leishmaniasis visual epilepsy vitiligo
27315	post-GPI attachment to proteins 2	PGAP2 Aliases: CWH43-N FGF receptor activating protein 1 FRAG1 cell wall biogenesis 43 N-terminal homolog (S. cerevisiae)	Homo sapiens (human)	Beckwith-Wiedemann syndrome CLOVES syndrome Cogan syndrome Hirschsprung's disease Perlman syndrome Sotos syndrome Unverricht-Lundborg syndrome blepharospasm bone osteosarcoma cancer capillary disease childhood osteosarcoma cleft palate craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy embryoma esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 3 hyperphosphatemia intellectual disability isolated cleft palate learning disability monocular esotropia oligohydramnios osteosarcoma scoliosis sensorineural hearing loss syndromic X-linked intellectual disability 94 telangiectasis visual epilepsy
10449	acetyl-CoA acyltransferase 2	ACAA2 Aliases: DSAEC mitochondrial 3-oxoacyl-Coenzyme A thiolase	Homo sapiens (human)	adult respiratory distress syndrome arthritis arthropathy beta-ketothiolase deficiency hepatocellular carcinoma liver cancer newborn respiratory distress syndrome osteoarthritis
2523	fucosyltransferase 1 (H blood group)	FUT1 Aliases: galactoside 2-alpha-L-fucosyltransferase	Homo sapiens (human)	B-cell lymphoma Edwards syndrome Fanconi anemia complementation group A Fanconi anemia complementation group D2 Fanconi anemia Kawasaki disease MHC class II deficiency Scheie syndrome T-cell acute lymphoblastic leukemia Wiskott-Aldrich syndrome X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 X-linked severe combined immunodeficiency acquired immunodeficiency syndrome acquired polycythemia acute myeloid leukemia acute promyelocytic leukemia adenosine deaminase deficiency adrenoleukodystrophy alcoholic hepatitis alcoholic liver cirrhosis anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome azoospermia beta thalassemia bile duct adenocarcinoma bile duct carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma 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 cerebral infarction cerebrovascular disease childhood leukemia cholangiocarcinoma chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined T cell and B cell immunodeficiency congenital hemolytic anemia cutaneous porphyria cystic fibrosis diarrhea distal arthrogryposis embryoma erythropoietic protoporphyria erythropoietin polycythemia essential thrombocythemia factor VIII deficiency familial erythrocytosis 2 gallbladder disease glycogen storage disease II head and neck squamous cell carcinoma hematologic cancer hematopoietic system disease hemochromatosis type 1 hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hemophagocytic lymphohistiocytosis hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease immune system disease inherited metabolic disorder intrahepatic cholangiocarcinoma juvenile myelomonocytic leukemia large intestine cancer leukemia liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma lysosomal storage disease macrocytic anemia malignant teratoma mantle cell lymphoma mature teratoma melanoma metachromatic leukodystrophy mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm obsolete ymphosarcoma orofaciodigital syndrome VIII osteoarthritis ovarian cancer ovarian carcinoma pancytopenia paroxysmal nocturnal hemoglobinuria polycythemia vera polycythemia progressive muscular atrophy prostate cancer prostate carcinoma proteinuria psoriatic arthritis sarcomatoid carcinoma severe combined immunodeficiency sickle cell anemia skin benign neoplasm skin cancer skin melanoma skin squamous cell carcinoma spinal muscular atrophy squamous cell carcinoma stomach cancer stomach carcinoma stress polycythemia teratocarcinoma teratoma tongue squamous cell carcinoma
51266	C-type lectin domain family 1 member B	CLEC1B Aliases: CLEC-2 CLEC2	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 Evans' syndrome Marfan syndrome Pick's disease Reye syndrome adult respiratory distress syndrome androgen insensitivity syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autoimmune thrombocytopenic purpura bacterial sepsis blood coagulation disease cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma gallbladder disease hematopoietic system disease hemolytic-uremic syndrome hepatocellular carcinoma liver cancer liver disease lung benign neoplasm melanoma newborn respiratory distress syndrome nonpapillary renal cell carcinoma nutmeg liver obsolete inherited blood coagulation disease papillary renal cell carcinoma pneumonia renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma situs inversus skin melanoma split hand-foot malformation 1 stomach cancer stomach carcinoma thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia thrombotic thrombocytopenic purpura tuberous sclerosis type 2 diabetes mellitus viral infectious disease

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements