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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	October 29, 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 **419201 - 419225** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
7975	MAF bZIP transcription factor K	MAFK	Homo sapiens (human)
7957	EPM2A glucan phosphatase, laforin	EPM2A Aliases: LD LDE	Homo sapiens (human)	Alzheimer's disease Balo concentric sclerosis Dravet syndrome Lafora disease MERRF syndrome Rett syndrome Unverricht-Lundborg syndrome adrenoleukodystrophy adult lymphoma agnosia alexia apraxia benign epilepsy with centrotemporal spikes blepharospasm blindness cancer central nervous system disease central nervous system lymphoma cerebral degeneration childhood lymphoma cystinuria dementia dentatorubral-pallidoluysian atrophy depressive disorder dyslexia dysthymic disorder early myoclonic encephalopathy embryoma endometrial carcinoma epilepsy focal hand dystonia galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease intellectual disability learning disability lymphoma major depressive disorder melancholic depression narcolepsy neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder non-syndromic X-linked intellectual disability obsolete Dravet syndrome obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma photosensitive epilepsy photosensitivity disease progressive myoclonus epilepsy 1A progressive myoclonus epilepsy 4 progressive myoclonus epilepsy psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder status epilepticus
7942	transcription factor EB	TFEB	Homo sapiens (human)
7941	phospholipase A2 group VII	PLA2G7 Aliases: LDL-PLA2 PAFAH	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 IgA glomerulonephritis Kawasaki disease Norum disease Pick's disease Reye syndrome Tangier disease X-linked dilated cardiomyopathy abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acoustic neuroma acquired immunodeficiency syndrome acute chest syndrome acute myocardial infarction acute pancreatitis adult respiratory distress syndrome allergic asthma allergic rhinitis amyloidosis angiomatous meningioma aortic valve disease 1 aortic valve disease aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation background diabetic retinopathy bacterial sepsis benign meningioma bicuspid aortic valve disease blind loop syndrome brain stem infarction cancer cardiomyopathy cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cerebral artery occlusion cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease choreaacanthocytosis clear cell meningioma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure coronary artery disease coronary artery vasospasm coronary thrombosis dementia depressive disorder dermatitis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic macular edema diabetic retinopathy 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 distal arthrogryposis end stage renal disease endomyocardial fibrosis essential hypertension exudative vitreoretinopathy familial adenomatous polyposis 1 familial adenomatous polyposis familial hypercholesterolemia familial hyperlipidemia familial hypertrophic cardiomyopathy familial hypobetalipoproteinemia 1 familial nephrotic syndrome fibrous meningioma generalized atherosclerosis gestational diabetes glomerulonephritis glomerulosclerosis heart disease hemolytic-uremic syndrome human immunodeficiency virus infectious disease hypertension hypertrophic cardiomyopathy hyperuricemia hypobetalipoproteinemia hypolipoproteinemia inflammatory bowel disease 1 inflammatory bowel disease inherited metabolic disorder intraorbital meningioma intraventricular meningioma intrinsic asthma islet cell tumor kidney failure large intestine cancer lipoid nephrosis meningioma meningothelial meningioma metabolic dysfunction-associated steatotic liver disease microcystic meningioma multiple sclerosis myocardial infarction nasopharynx carcinoma nephrotic syndrome type 2 nephrotic syndrome newborn respiratory distress syndrome nutmeg liver obesity obsolete eye and adnexa disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea olfactory groove meningioma pancreatitis parapsoriasis parasagittal meningioma peripheral artery disease pituitary adenoma polycystic ovary syndrome primary pulmonary hypertension proliferative diabetic retinopathy prostate cancer prostate carcinoma proteinuria psammomatous meningioma psoriasis pulmonary hypertension pustulosis of palm and sole retinal disease retinitis rheumatoid arthritis schizophrenia secretory meningioma silent myocardial infarction spinal meningioma steatotic liver disease transient cerebral ischemia transitional meningioma 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 uremia vascular disease vasomotor rhinitis vertebrobasilar insufficiency
7936	negative elongation factor complex member E	NELFE	Homo sapiens (human)
7932	olfactory receptor family 2 subfamily H member 2	OR2H2	Homo sapiens (human)
7923	hydroxysteroid 17-beta dehydrogenase 8	HSD17B8 Aliases: D6S2245E H2-KE6 HKE6 KE6 RING2 SDR30C1 short chain dehydrogenase/reductase family 30C, member 1	Homo sapiens (human)	breast cancer breast carcinoma cancer hepatitis B rheumatoid arthritis tuberculosis
7922	solute carrier family 39 member 7	SLC39A7	Homo sapiens (human)
7917	BAG cochaperone 6	BAG6	Homo sapiens (human)
7916	proline rich coiled-coil 2A	PRRC2A	Homo sapiens (human)
7915	aldehyde dehydrogenase 5 family member A1	ALDH5A1 Aliases: SSADH SSDH succinate-semialdehyde dehydrogenase	Homo sapiens (human)	Crohn's colitis Crohn's disease Rett syndrome X-linked dystonia-parkinsonism Zika fever age related macular degeneration agnosia anxiety disorder autistic disorder carcinoma degeneration of macula and posterior pole developmental coordination disorder dystonia 12 dystonia 16 dystonia 21 dystonia 25 dystonia 27 dystonia 5 dystonia epilepsy focal dystonia focal hand dystonia generalized anxiety disorder generalized dystonia generalized epilepsy with febrile seizures plus hypertropia idiopathic generalized epilepsy inflammatory bowel disease 1 inflammatory bowel disease intellectual disability juvenile myoclonic epilepsy learning disability lingual-facial-buccal dyskinesia macular degeneration mechanical strabismus movement disease myoclonic dystonia 11 ophthalmoplegia ovarian cancer ovarian carcinoma psychotic disorder schizoaffective disorder schizophreniform disorder status epilepticus strabismus succinic semialdehyde dehydrogenase deficiency syndromic X-linked intellectual disability 94 torsion dystonia 13 torsion dystonia 17 torsion dystonia 1 torsion dystonia 2 torsion dystonia 4 torsion dystonia 6 torsion dystonia with onset in infancy tuberculosis ulcerative colitis visual epilepsy
7913	DEK proto-oncogene	DEK	Homo sapiens (human)
7903	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	ST8SIA4 Aliases: PST PST1 ST8Sia IV	Homo sapiens (human)	Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Norum disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Tangier disease abetalipoproteinemia acne acute pancreatitis adrenoleukodystrophy alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alternating hemiplegia of childhood anal carcinoma in situ anaplastic astrocytoma ankylosing spondylitis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer breast carcinoma bronchus cancer bronchus carcinoma bulimia nervosa cancer carcinoma carotid artery thrombosis carotid stenosis central nervous system disease cerebral infarction cerebrovascular disease cervix uteri carcinoma in situ childhood cerebral astrocytoma childhood leukemia cholecystolithiasis choledocholithiasis cholelithiasis choreaacanthocytosis chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma complement deficiency coronary artery disease depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diarrhea dysthymic disorder embryoma esophageal cancer esophageal carcinoma essential hypertension fibrillary astrocytoma fragile X syndrome gallbladder cancer gallbladder carcinoma gallbladder disease gemistocytic astrocytoma giant cell glioblastoma glioblastoma glomerulonephritis gyrate atrophy hepatocellular carcinoma hereditary spherocytosis high grade glioma hypertension hypolipoproteinemia hypoparathyroidism juvenile pilocytic astrocytoma kidney disease large intestine cancer laryngeal squamous cell carcinoma leukemia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma major depressive disorder malignant astrocytoma melancholic depression muscular dystrophy myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nephritis nervous system disease neuroblastoma neurotic disorder nonpapillary renal cell carcinoma nutmeg liver obsolete melancholia pancreatitis papillary renal cell carcinoma papilloma periodontitis pilocytic astrocytoma pneumonia prostate cancer prostate carcinoma protoplasmic astrocytoma pseudohypoparathyroidism renal carcinoma renal cell carcinoma rhabdomyosarcoma rhinitis sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sinusitis squamous cell carcinoma squamous cell papilloma steatotic liver disease subependymal giant cell astrocytoma substance abuse substance-related disorder systemic lupus erythematosus thyroid gland follicular carcinoma tongue squamous cell carcinoma type 2 diabetes mellitus uveoparotid fever
7879	RAB7A, member RAS oncogene family	RAB7A	Homo sapiens (human)
7874	ubiquitin specific peptidase 7	USP7	Homo sapiens (human)
7871	sarcolemma associated protein	SLMAP	Homo sapiens (human)
7869	semaphorin 3B	SEMA3B	Homo sapiens (human)
7866	interferon related developmental regulator 2	IFRD2	Homo sapiens (human)
7862	bromodomain and PHD finger containing 1	BRPF1	Homo sapiens (human)
7855	frizzled class receptor 5	FZD5	Homo sapiens (human)
7852	C-X-C motif chemokine receptor 4	CXCR4	Homo sapiens (human)
7850	interleukin 1 receptor type 2	IL1R2	Homo sapiens (human)
7849	paired box 8	PAX8	Homo sapiens (human)
7846	tubulin alpha 1a	TUBA1A Aliases: B-ALPHA-1 FLJ25113 TUBA3 tubulin, alpha, brain-specific	Homo sapiens (human)
7841	mannosyl-oligosaccharide glucosidase	MOGS Aliases: CWH41 DER7 GCS1 glucosidase I processing A-glucosidase I	Homo sapiens (human)	Japanese encephalitis Turner syndrome Zika fever acquired hyperkeratosis actinic keratosis acute lymphoblastic leukemia acute myeloid leukemia adamantinoma agammaglobulinemia ameloblastoma blepharophimosis bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic monocytic leukemia chronic myelomonocytic leukemia congenital disorder of glycosylation In congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIb congenital disorder of glycosylation cystic fibrosis dengue disease epilepsy gonadal dysgenesis holoprosencephaly 1 holoprosencephaly juvenile myelomonocytic leukemia keratoacanthoma lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma malaria melanoma obesity optic atrophy pleomorphic xanthoastrocytoma sensorineural hearing loss skin melanoma viral infectious disease visual epilepsy yellow fever

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