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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 **8351 - 8375** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
115209	OMA1 zinc metallopeptidase	OMA1	Homo sapiens (human)
4952	OCRL inositol polyphosphate-5-phosphatase	OCRL Aliases: Dent disease 2 Dent-2 OCRL1	Homo sapiens (human)	Bartter disease Conn's syndrome Dent disease Ehlers-Danlos syndrome Fanconi anemia Fanconi syndrome Laron syndrome Waterhouse-Friderichsen syndrome achondroplasia amblyopia anemia angular cheilitis anxiety disorder arthritis arthropathy attention deficit hyperactivity disorder autistic disorder autoimmune hemolytic anemia azoospermia blindness buphthalmos calcinosis calcium metabolism disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cheilitis chromosome 17p13.1 deletion syndrome chronic kidney disease chronic ulcer of skin congenital nystagmus cryptorchidism cystinosis dental caries dental enamel hypoplasia dentin caries depressive disorder diabetes insipidus dissociated nystagmus dysthymic disorder epilepsy esophagitis fetal erythroblastosis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma gingivitis glaucoma glioblastoma glomerulonephritis high grade glioma hydrocephalus hydrophthalmos hypercalcemia hyperparathyroidism hypertropia hypokalemia hypophosphatemia inguinal hernia intellectual disability isolated elevated serum creatine phosphokinase levels kidney failure learning disability lip disease lissencephaly listeriosis macrocytic anemia major depressive disorder mechanical strabismus melancholic depression microphthalmia neonatal anemia nephritis nephrocalcinosis nephrolithiasis neurohypophyseal diabetes insipidus neurotic disorder obsolete constipation obsolete melancholia oculocerebrorenal syndrome omphalocele ophthalmoplegia osteitis fibrosa osteoarthritis osteogenesis imperfecta osteomalacia otitis media pathologic nystagmus peptic esophagitis periodontitis phosphorus metabolism disease primary hyperaldosteronism proteinuria recurrent corneal erosion renal tubular acidosis rickets scoliosis skin benign neoplasm skin cancer spondyloepimetaphyseal dysplasia, Sponastrime type spontaneous ocular nystagmus stereotypic movement disorder strabismic amblyopia strabismus subcortical band heterotopia thrombocytopenia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue umbilical hernia uremia uric acid nephrolithiasis visual epilepsy
54940	OCIA domain containing 1	OCIAD1	Homo sapiens (human)
4948	OCA2 melanosomal transmembrane protein	OCA2	Homo sapiens (human)
55644	O-sialoglycoprotein endopeptidase	OSGEP	Homo sapiens (human)
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
221443	O-acyl-ADP-ribose deacylase 1	OARD1 Aliases: MGC19570 TARG1 dJ34B21.3 terminal ADP-ribose protein glycohydrolase 1	Homo sapiens (human)	acute myeloid leukemia neurodegenerative disease stomach cancer stomach carcinoma
10724	O-GlcNAcase	OGA Aliases: MEA5 NCOAT nuclear cytoplasmic O-GlcNAcase and acetyltransferase	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 Fabry disease GM1 gangliosidosis GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Gilles de la Tourette syndrome Lewy body dementia Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute myocardial infarction alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis angiomatous meningioma anterior horn cell disease aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive distal hereditary motor neuronopathy 1 benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease cerebral convexity meningioma cerebral degeneration chronic kidney disease chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis cystitis dermatitis diabetes mellitus diabetic ketoacidosis dystonia embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma essential hypertension fibrous meningioma gangliosidosis gastroenteritis gastrointestinal system disease gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis glucose intolerance glycoproteinosis heart disease hepatocellular carcinoma hydronephrosis hypertension ileitis ileocolitis intestinal disease intraorbital meningioma intraventricular meningioma kidney disease kidney failure kwashiorkor large intestine cancer lateral sclerosis lingual-facial-buccal dyskinesia lipid storage disease lipoid nephrosis liver cancer liver cirrhosis long QT syndrome 8 lung cancer lung carcinoma lymphoplasmacyte-rich meningioma lysosomal storage disease marasmus membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia motor neuron disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IVB mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple myeloma myelitis myocardial infarction nephritis nephrosis nervous system disease neurodegenerative disease nutrition disease obesity obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 olfactory groove meningioma ovarian cancer ovarian carcinoma panic disorder parasagittal meningioma pituitary adenoma prediabetes syndrome progressive familial intrahepatic cholestasis 1 progressive muscular atrophy progressive supranuclear palsy protein-energy malnutrition psammomatous meningioma pyoureter renal osteodystrophy retrograde amnesia sarcoma secondary Parkinson disease secretory meningioma silent myocardial infarction situs inversus sphingolipidosis spinal meningioma spindle cell sarcoma tauopathy thalassemia transitional meningioma tricuspid valve stenosis trigonitis tuberous sclerosis 1 tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus visual epilepsy
4255	O-6-methylguanine-DNA methyltransferase	MGMT	Homo sapiens (human)
134492	NudC domain containing 2	NUDCD2	Homo sapiens (human)
84955	NudC domain containing 1	NUDCD1	Homo sapiens (human)
203447	Nik related kinase	NRK	Homo sapiens (human)
57523	NYN domain and retroviral integrase containing	NYNRIN	Homo sapiens (human)
256646	NUT midline carcinoma family member 1	NUTM1	Homo sapiens (human)
116150	NUS1 dehydrodolichyl diphosphate synthase subunit	NUS1	Homo sapiens (human)
9253	NUMB like endocytic adaptor protein	NUMBL	Homo sapiens (human)
83540	NUF2 component of NDC80 kinetochore complex	NUF2	Homo sapiens (human)
10101	NUBP iron-sulfur cluster assembly factor 2, cytosolic	NUBP2	Homo sapiens (human)
4682	NUBP iron-sulfur cluster assembly factor 1, cytosolic	NUBP1	Homo sapiens (human)
81788	NUAK family kinase 2	NUAK2	Homo sapiens (human)
8775	NSF attachment protein alpha	NAPA	Homo sapiens (human)
54780	NSE4 homolog A, SMC5-SMC6 complex component	NSMCE4A	Homo sapiens (human)
10412	NSA2 ribosome biogenesis factor	NSA2	Homo sapiens (human)
55051	NRDE-2, necessary for RNA interference, domain containing	NRDE2	Homo sapiens (human)
4893	NRAS proto-oncogene, GTPase	NRAS Aliases: N-ras	Homo sapiens (human)

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