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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 **7926 - 7950** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
728819	C1GALT1 specific chaperone 1 like	C1GALT1C1L	Homo sapiens (human)
58503	opiorphin prepropeptide	OPRPN	Homo sapiens (human)
93081	testis expressed 30	TEX30	Homo sapiens (human)
4851	notch receptor 1	NOTCH1	Homo sapiens (human)
78990	OTU deubiquitinase, ubiquitin aldehyde binding 2	OTUB2	Homo sapiens (human)
51368	testis expressed 264, ER-phagy receptor	TEX264	Homo sapiens (human)
3021	H3.3 histone B	H3-3B	Homo sapiens (human)
7401	clarin 1	CLRN1	Homo sapiens (human)
3681	integrin subunit alpha D	ITGAD	Homo sapiens (human)
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)
8315	BRCA1 associated protein	BRAP	Homo sapiens (human)
26085	kallikrein related peptidase 13	KLK13	Homo sapiens (human)
1407	cryptochrome circadian regulator 1	CRY1	Homo sapiens (human)	delayed sleep phase syndrome
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
731	complement C8 alpha chain	C8A	Homo sapiens (human)
26115	tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2	TANC2	Homo sapiens (human)
2821	glucose-6-phosphate isomerase	GPI Aliases: AMF NLK	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 Cornelia de Lange syndrome Creutzfeldt-Jakob disease Down 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 Parkinson's disease Pick's disease Plasmodium vivax malaria Prader-Willi syndrome Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adult fibrosarcoma adult lymphoma alternating hemiplegia of childhood anemia antiphospholipid syndrome aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrophic gastritis atypical hemolytic-uremic syndrome autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome benign mesothelioma blastomycosis bone osteosarcoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system disease central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood lymphoma childhood osteosarcoma cholecystitis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic fatigue syndrome chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common cold congenital diaphragmatic hernia congenital disorder of glycosylation congenital hemolytic anemia congenital nonspherocytic hemolytic anemia coronary artery disease coronary thrombosis cystinuria depressive disorder diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma diffuse large B-cell lymphoma dysthymic disorder dystonia embryoma encephalitis encephalomyelitis endocarditis endometrial cancer endometrial carcinoma essential hypertension essential thrombocythemia familial retinoblastoma favism female stress incontinence fetal erythroblastosis fibrosarcoma focal hand dystonia galactosemia generalized dystonia giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease head and neck squamous cell carcinoma heart disease hematologic cancer hemoglobinopathy hemolytic anemia hemolytic-uremic syndrome hepatitis B hepatitis hepatocellular carcinoma hereditary elliptocytosis high grade glioma human immunodeficiency virus infectious disease hypertension immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease infective endocarditis inflammatory and toxic neuropathy influenza intellectual disability intracranial embolism large intestine cancer learning disability leukemia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lupus erythematosus lymphoma macrocytic anemia major depressive disorder malignant hyperthermia malignant mesothelioma melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia migraine mixed glioma multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction neonatal anemia neonatal jaundice nervous system disease neurogenic arthropathy neuromuscular disease neurotic disorder nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pancytopenia papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis paroxysmal nocturnal hemoglobinuria peeling skin syndrome placental insufficiency platelet-type bleeding disorder 3 pre-eclampsia primary immunodeficiency disease primary pulmonary hypertension prion disease pure red-cell aplasia renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinoblastoma rheumatoid arthritis sarcomatoid renal cell carcinoma scleroderma silent myocardial infarction skin atrophy steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis syndromic X-linked intellectual disability Snyder type syndromic intellectual disability synovitis systemic lupus erythematosus systemic scleroderma tenosynovitis thrombophilia thrombotic thrombocytopenic purpura thyroid gland anaplastic carcinoma thyroid gland papillary carcinoma trilateral retinoblastoma 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 uterine corpus cancer vascular dementia vascular disease viral infectious disease von Willebrand's disease
4330	MN1 proto-oncogene, transcriptional regulator	MN1	Homo sapiens (human)
8664	eukaryotic translation initiation factor 3 subunit D	EIF3D	Homo sapiens (human)
341799	olfactory receptor family 6 subfamily S member 1	OR6S1	Homo sapiens (human)
146754	dynein axonemal heavy chain 2	DNAH2	Homo sapiens (human)
5606	mitogen-activated protein kinase kinase 3	MAP2K3	Homo sapiens (human)
109	adenylate cyclase 3	ADCY3	Homo sapiens (human)
219493	olfactory receptor family 5 subfamily AR member 1	OR5AR1	Homo sapiens (human)
333926	protein phosphatase, Mg2+/Mn2+ dependent 1J	PPM1J	Homo sapiens (human)

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