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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 **7801 - 7825** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
4976	OPA1 mitochondrial dynamin like GTPase	OPA1 Aliases: Dynamin-like 120 kDa protein, mitochondrial FLJ12460 KIAA0567 MGM1 NPG NTG dynamin-like guanosine triphosphatase mitochondrial dynamin-like GTPase	Homo sapiens (human)
4974	oligodendrocyte myelin glycoprotein	OMG	Homo sapiens (human)
4973	oxidized low density lipoprotein receptor 1	OLR1 Aliases: CLEC8A LOX-1 SCARE1	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 Cockayne syndrome Kawasaki disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis acute chest syndrome acute myocardial infarction adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation bone osteosarcoma brain stem infarction breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease carpal tunnel syndrome central sleep apnea cerebral amyloid angiopathy cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma choriocarcinoma chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma end stage renal disease endomyocardial fibrosis essential hypertension familial hypercholesterolemia familial hyperlipidemia gallbladder disease generalized atherosclerosis gestational diabetes giant cell glioblastoma glioblastoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma hyperhomocysteinemia hypertension hypertrophic cardiomyopathy juvenile rheumatoid arthritis keratitis keratoconjunctivitis kidney failure large intestine cancer liver cancer liver disease lung adenocarcinoma lung cancer multiple sclerosis multiple system atrophy myocardial infarction nutmeg liver obesity osteoarthritis osteosarcoma pancreatic cancer pancreatic carcinoma parapsoriasis placenta cancer postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole renal osteodystrophy rheumatoid arthritis seborrheic keratosis sickle cell anemia silent myocardial infarction skin disease transient cerebral ischemia tubular adenocarcinoma type 2 diabetes mellitus vascular disease vertebrobasilar insufficiency
4969	osteoglycin	OGN	Homo sapiens (human)
4968	8-oxoguanine DNA glycosylase	OGG1 Aliases: 8-hydroxyguanine DNA glycosylase HMMH HOGG1 MUTM OGG1 type 1d OGG1 type 1e OGG1 type 1g OGG1 type 1h OGH1	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 Barrett's esophagus Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Holt-Oram syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Klippel-Trenaunay syndrome Langerhans-cell histiocytosis Marfan 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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome Rubinstein-Taybi syndrome Seckel syndrome Silver-Russell syndrome T-cell acute lymphoblastic leukemia VACTERL association Werner syndrome X-linked Aarskog syndrome abdominal obesity-metabolic syndrome 1 acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute biphenotypic leukemia acute chest syndrome acute leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adult hepatocellular carcinoma age related macular degeneration allergic asthma anal carcinoma in situ angiomyolipoma angle-closure glaucoma anthracosilicosis anthracosis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asbestosis asthma ataxia with oculomotor apraxia type 1 atherosclerosis atrophic gastritis autism spectrum disorder autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bacterial infectious disease bacterial meningitis basal cell carcinoma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder transitional cell papilloma bone marrow cancer brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cataract central nervous system lymphoma cerebellar ataxia cerebellar disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder developmental coordination disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism distal arthrogryposis duodenum disease dysthymic disorder embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis esophageal cancer esophageal carcinoma esophageal disease esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exocrine pancreatic insufficiency familial adenomatous polyposis 1 familial adenomatous polyposis female breast carcinoma follicular adenoma follicular lymphoma gallbladder adenocarcinoma gallbladder cancer gallbladder carcinoma gallbladder disease gastric cardia adenocarcinoma gastric diffuse adenocarcinoma gastrointestinal system cancer gestational diabetes glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma human immunodeficiency virus infectious disease hyperglycemia hypertension hyperthyroidism idiopathic interstitial pneumonia inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intrinsic asthma islet cell tumor keratosis kidney angiomyolipoma kidney cancer kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer late onset Parkinson's disease leiomyoma leukemia liver cancer liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lupus nephritis lymphoma macular degeneration major depressive disorder male infertility melancholic depression melanoma meningitis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia with limb anomalies middle cerebral artery infarction mitochondrial metabolism disease mitochondrial myopathy multiple sclerosis myelodysplastic syndrome myeloid sarcoma myeloproliferative neoplasm myocardial infarction myofibroma nail-patella syndrome nasopharynx carcinoma nephritis nephroblastoma neurodegenerative disease neurotic disorder non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver obesity obsolete melancholia obsolete ymphosarcoma oral mucosa leukoplakia ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panic disorder papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma postinflammatory pulmonary fibrosis pre-eclampsia primary angle-closure glaucoma primary open angle glaucoma prion disease progeria progressive supranuclear palsy propionic acidemia prostate cancer prostate carcinoma pterygium pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis senile cataract silent myocardial infarction situs inversus skin benign neoplasm skin cancer skin disease skin melanoma split hand-foot malformation 1 with sensorineural hearing loss sporadic breast cancer squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma stomach disease systemic lupus erythematosus thrombocytopenia-absent radius syndrome thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transient cerebral ischemia transitional cell carcinoma tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus tyrosinemia type I tyrosinemia ulcerative colitis urinary bladder cancer urinary system benign neoplasm urinary system cancer uterine corpus cancer uterine fibroid varicocele vertebrobasilar insufficiency viral meningitis white sponge nevus xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
4967	oxoglutarate dehydrogenase	OGDH Aliases: E1k KGD1 OGDC-E1 OGDH2	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 Laron syndrome Leigh disease Pick's disease Reye syndrome Yoon-Bellen neurodevelopmental syndrome achondroplasia alternating hemiplegia of childhood arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer cancer central nervous system disease cerebral degeneration colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease embryoma hydrocephalus lactic acidosis large intestine cancer lingual-facial-buccal dyskinesia movement disease nervous system disease neuroblastoma neurodegenerative disease obstructive hydrocephalus oxoglutarate dehydrogenase deficiency phenylketonuria placental insufficiency primary biliary cholangitis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency senile degeneration of brain status epilepticus urea cycle disorder viral infectious disease
4958	osteomodulin	OMD	Homo sapiens (human)
4957	outer dense fiber of sperm tails 2	ODF2	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
4948	OCA2 melanosomal transmembrane protein	OCA2	Homo sapiens (human)
4943	TBC1 domain family member 25	TBC1D25	Homo sapiens (human)
4940	2'-5'-oligoadenylate synthetase 3	OAS3	Homo sapiens (human)
4938	2'-5'-oligoadenylate synthetase 1	OAS1	Homo sapiens (human)	primary immunodeficiency disease
4935	G protein-coupled receptor 143	GPR143	Homo sapiens (human)
4931	nuclear VCP like	NVL	Homo sapiens (human)
4928	nucleoporin 98 and 96 precursor	NUP98	Homo sapiens (human)
4926	nuclear mitotic apparatus protein 1	NUMA1	Homo sapiens (human)
4925	nucleobindin 2	NUCB2	Homo sapiens (human)
4924	nucleobindin 1	NUCB1	Homo sapiens (human)
4923	neurotensin receptor 1	NTSR1	Homo sapiens (human)
4921	discoidin domain receptor tyrosine kinase 2	DDR2	Homo sapiens (human)
4920	receptor tyrosine kinase like orphan receptor 2	ROR2	Homo sapiens (human)
4919	receptor tyrosine kinase like orphan receptor 1	ROR1	Homo sapiens (human)
4917	netrin 3	NTN3	Homo sapiens (human)
4916	neurotrophic receptor tyrosine kinase 3	NTRK3	Homo sapiens (human)

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