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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 **9226 - 9250** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
92285	zinc finger protein 585B	ZNF585B	Homo sapiens (human)
9019	myelin protein zero like 1	MPZL1	Homo sapiens (human)
387836	C-type lectin domain family 2 member A	CLEC2A	Homo sapiens (human)
23601	C-type lectin domain containing 5A	CLEC5A Aliases: MDL-1	Homo sapiens (human)	Japanese encephalitis Mycoplasma pneumoniae pneumonia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis bone osteosarcoma brain glioblastoma multiforme central nervous system cancer cholesteatoma dengue disease dengue hemorrhagic fever giant cell glioblastoma glioblastoma gliosarcoma high grade glioma mixed glioma osteoarthritis osteosarcoma polyp of middle ear viral infectious disease yellow fever
2687	gamma-glutamyltransferase 5	GGT5 Aliases: GGT-REL	Homo sapiens (human)	hepatocellular carcinoma liver cancer lung benign neoplasm
390154	olfactory receptor family 5 subfamily T member 3	OR5T3	Homo sapiens (human)
167127	UDP glycosyltransferase family 3 member A2	UGT3A2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
10131	TNF receptor associated protein 1	TRAP1	Homo sapiens (human)
4886	neuropeptide Y receptor Y1	NPY1R	Homo sapiens (human)	amphetamine abuse anxiety disorder childhood absence epilepsy cocaine abuse depressive disorder heroin dependence hypertension nicotine dependence obesity opiate dependence peripheral artery disease temporal lobe epilepsy visual epilepsy
29800	zinc finger DHHC-type containing 1	ZDHHC1	Homo sapiens (human)
170506	DEAH-box helicase 36	DHX36	Homo sapiens (human)
5824	peroxisomal biogenesis factor 19	PEX19	Homo sapiens (human)
1545	cytochrome P450 family 1 subfamily B member 1	CYP1B1 Aliases: CP1B	Homo sapiens (human)	Axenfeld-Rieger syndrome B-cell lymphoma Bloch-Sulzberger syndrome Foster-Kennedy syndrome Langerhans-cell histiocytosis Lynch syndrome Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peters anomaly Peutz-Jeghers syndrome Sveinsson chorioretinal atrophy acoustic neuroma acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult medulloblastoma adult respiratory distress syndrome agranulocytosis allergic asthma amnestic disorder anaplastic astrocytoma anemia angiomatous meningioma angle-closure glaucoma aniridia ankylosing spondylitis anterior segment dysgenesis 6 anterior segment dysgenesis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis 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 autism spectrum disorder autistic disorder basal cell carcinoma benign meningioma bladder carcinoma blindness brain cancer branch retinal artery occlusion breast adenocarcinoma breast cancer breast carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma buphthalmos cancer capillary hemangioma carcinoma cardiovascular system disease cavernous hemangioma central nervous system cancer central nervous system lymphoma central retinal artery occlusion cerebral convexity meningioma cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood kidney cell carcinoma childhood leukemia childhood medulloblastoma choriocarcinoma chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma coloboma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital nystagmus congestive heart failure contact dermatitis cornea plana corneal neovascularization coronary artery disease coronary thrombosis cribriform carcinoma depressive disorder diabetes mellitus disease of metabolism dissociated nystagmus dysplastic nevus syndrome ectropion embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia eye disease familial adenomatous polyposis familial hyperlipidemia familial multiple nevi flammei female breast carcinoma fibrillary astrocytoma fibrous meningioma follicular adenoma gallbladder cancer gallbladder carcinoma gallbladder disease gastrointestinal stromal tumor gemistocytic astrocytoma gestational diabetes giant cell glioblastoma glaucoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis hepatocellular carcinoma high grade glioma hydrophthalmos hyperglycemia hypertension hypertrophic cardiomyopathy hypertropia hypomelanosis of Ito hypospadias inflammatory breast carcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma juvenile glaucoma juvenile pilocytic astrocytoma kidney cancer large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer leiomyoma leukemia leukopenia liver cancer liver disease low tension glaucoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lymphoblastic lymphoma lymphoma lymphoplasmacyte-rich meningioma macrocytic anemia male breast cancer male infertility malignant astrocytoma mechanical strabismus medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma microglandular adenosis microphthalmia mixed glioma multiple myeloma multiple sclerosis myelodysplastic syndrome myocardial infarction myofibroma neutropenia newborn respiratory distress syndrome nodular prostate non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete anterior segment mesenchymal dysgenesis obsolete ymphosarcoma occupational dermatitis ocular hypertension oculodentodigital dysplasia olfactory groove meningioma open-angle glaucoma ophthalmoplegia optic atrophy 1 optic atrophy optic nerve disease oral mucosa leukoplakia osteoarthritis osteoporosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis papillary adenoma papillary renal cell carcinoma parasagittal meningioma patent ductus arteriosus patent foramen ovale pathologic nystagmus periodontitis phimosis pilocytic astrocytoma pituitary adenoma placenta cancer polycystic ovary syndrome prediabetes syndrome primary angle-closure glaucoma primary cutaneous amyloidosis primary open angle glaucoma primary pulmonary hypertension prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma psammomatous meningioma recurrent corneal erosion renal carcinoma renal cell carcinoma reticulosarcoma retinal artery occlusion retinal detachment retinal disease retinal vein occlusion retinitis retrograde amnesia sarcomatoid carcinoma sarcomatoid renal cell carcinoma sebaceous carcinoma secretory meningioma severe congenital neutropenia silent myocardial infarction situs inversus skin melanoma spinal meningioma spontaneous ocular nystagmus squamous cell carcinoma squamous cell neoplasm steatotic liver disease strabismus subependymal giant cell astrocytoma sweat gland cancer tongue squamous cell carcinoma transitional cell carcinoma transitional meningioma tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer uterine fibroid visual pathway disease von Hippel-Lindau disease 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
1635	dCMP deaminase	DCTD	Homo sapiens (human)	breast cancer cancer esophagus squamous cell carcinoma gliosarcoma high grade glioma leukopenia mixed glioma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma
53942	contactin 5	CNTN5 Aliases: NB-2 hNB-2	Homo sapiens (human)	Behcet's disease Hirschsprung's disease Parkinson's disease 2 anorexia nervosa atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder communicating hydrocephalus congestive heart failure depressive disorder differentiated thyroid gland carcinoma essential hypertension gout hydrocephalus hypertension major depressive disorder melancholic depression neurotic disorder obsolete melancholia obstructive hydrocephalus primary biliary cholangitis schizophrenia senile degeneration of brain
64063	serine protease 22	PRSS22	Homo sapiens (human)
56996	solute carrier family 12 member 9	SLC12A9	Homo sapiens (human)
23586	RNA sensor RIG-I	RIGI	Homo sapiens (human)
57634	E1A binding protein p400	EP400	Homo sapiens (human)
8666	eukaryotic translation initiation factor 3 subunit G	EIF3G	Homo sapiens (human)
4772	nuclear factor of activated T cells 1	NFATC1	Homo sapiens (human)
57572	dedicator of cytokinesis 6	DOCK6	Homo sapiens (human)
64601	VPS16 core subunit of CORVET and HOPS complexes	VPS16	Homo sapiens (human)
225	ATP binding cassette subfamily D member 2	ABCD2 Aliases: ALDR ALDRP	Homo sapiens (human)
79799	UDP glucuronosyltransferase family 2 member A3	UGT2A3 Aliases: FLJ21934	Homo sapiens (human)

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