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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 **7601 - 7625** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
504190	olfactory receptor family 8 subfamily U member 9	OR8U9	Homo sapiens (human)
8367	H4 clustered histone 5	H4C5	Homo sapiens (human)
388630	TraB domain containing 2B	TRABD2B	Homo sapiens (human)
49855	S-phase cyclin A associated protein in the ER	SCAPER	Homo sapiens (human)
80351	tankyrase 2	TNKS2 Aliases: ARTD6 PARP-5b PARP-5c PARP5B PARP5C TANK2 TNKL TRF1-interacting ankyrin-related ADP-ribose polymerase 2 pART6	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma basal cell carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma cleft lip cribriform carcinoma depressive disorder diabetes mellitus endometrial cancer endometrial carcinoma granular cell carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia osteosarcoma skin benign neoplasm skin cancer squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uterine corpus cancer
4486	macrophage stimulating 1 receptor	MST1R	Homo sapiens (human)
5001	origin recognition complex subunit 5	ORC5	Homo sapiens (human)
10634	growth arrest specific 2 like 1	GAS2L1	Homo sapiens (human)
1579	cytochrome P450 family 4 subfamily A member 11	CYP4A11 Aliases: CYP4AII	Homo sapiens (human)	Meckel syndrome acute myocardial infarction alcoholic liver cirrhosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease brain stem infarction cancer cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis embryoma essential hypertension hepatocellular carcinoma hypertension liver cancer liver cirrhosis myocardial infarction nephrosclerosis nutmeg liver renal artery disease renal hypertension silent myocardial infarction steatotic liver disease varicose veins
3460	interferon gamma receptor 2	IFNGR2	Homo sapiens (human)
5239	phosphoglucomutase 5	PGM5 Aliases: PGMRP phosphoglucomutase-related protein	Homo sapiens (human)	bladder carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer liver carcinoma urinary bladder cancer
170302	aristaless related homeobox	ARX	Homo sapiens (human)
3750	potassium voltage-gated channel subfamily D member 1	KCND1	Homo sapiens (human)
8927	bassoon presynaptic cytomatrix protein	BSN	Homo sapiens (human)
1910	endothelin receptor type B	EDNRB	Homo sapiens (human)
54847	SID1 transmembrane family member 1	SIDT1	Homo sapiens (human)
405754	endogenous retrovirus group FRD member 1, envelope	ERVFRD-1	Homo sapiens (human)
4038	LDL receptor related protein 4	LRP4	Homo sapiens (human)
6041	ribonuclease L	RNASEL	Homo sapiens (human)
9435	carbohydrate sulfotransferase 2	CHST2 Aliases: C6ST	Homo sapiens (human)	amyotrophic lateral sclerosis bone osteosarcoma cancer extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue gastric lymphoma inflammatory bowel disease 1 inflammatory bowel disease osteosarcoma progressive muscular atrophy ulcerative colitis
55247	nei like DNA glycosylase 3	NEIL3 Aliases: FLJ10858 FPG2 ZGRF3 hFPG2 hNEI3 zinc finger, GRF-type containing 3	Homo sapiens (human)	Fanconi anemia acute myocardial infarction basal cell carcinoma cancer coronary thrombosis differentiated thyroid gland carcinoma embryoma giant cell glioblastoma glioblastoma glomerulonephritis hepatocellular carcinoma kidney disease liver cancer myocardial infarction nephritis silent myocardial infarction
54805	cyclin and CBS domain divalent metal cation transport mediator 2	CNNM2	Homo sapiens (human)
6389	succinate dehydrogenase complex flavoprotein subunit A	SDHA Aliases: FP SDHF flavoprotein subunit of complex II succinate dehydrogenase [ubiquinone] flavoprotein subunit	Homo sapiens (human)	Laron syndrome Leigh disease Parkinson's disease Unverricht-Lundborg syndrome X-linked dilated cardiomyopathy achondroplasia adrenal gland cancer agnosia anaplastic astrocytoma anemia aniridia arthritis arthropathy ataxia with oculomotor apraxia type 1 attention deficit hyperactivity disorder benign breast phyllodes tumor blepharospasm blindness bone osteosarcoma brain disease breast cancer breast carcinoma breast malignant phyllodes tumor cancer cardiomyopathy cervical adenocarcinoma cervical cancer cervix carcinoma childhood astrocytic tumor childhood cerebral astrocytoma childhood osteosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm cone-rod dystrophy congenital diaphragmatic hernia congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital nystagmus congenital ptosis congestive heart failure dementia developmental coordination disorder diabetes mellitus 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 dissociated nystagmus duodenum cancer dystonia early myoclonic encephalopathy embryoma endomyocardial fibrosis epilepsy epithelioid sarcoma esophageal cancer esophageal carcinoma exanthem familial adenomatous polyposis familial hypertrophic cardiomyopathy familial periodic paralysis fibrillary astrocytoma focal hand dystonia fundus albipunctatus gastric adenocarcinoma gastrointestinal stromal tumor gemistocytic astrocytoma giant cell glioblastoma glioblastoma glomerulonephritis heart cancer hepatocellular carcinoma high grade glioma hypercalcemia hypertensive retinopathy hypertrichosis hypertrophic cardiomyopathy hypertropia ileus insulinoma intellectual disability intestinal obstruction islet cell tumor isolated elevated serum creatine phosphokinase levels juvenile pilocytic astrocytoma kidney disease lactic acidosis learning disability left ventricular noncompaction leukodystrophy lipoatrophic diabetes mellitus lipodystrophy liver cancer lung cancer lung non-small cell carcinoma macrocytic anemia malignant astrocytoma mechanical strabismus melanoma mitochondrial complex II deficiency mitochondrial metabolism disease mitochondrial myopathy multiple endocrine neoplasia type 1 myopathy nephritis nephrocalcinosis neuroblastoma neurodegenerative disease neuroendocrine carcinoma neuropathy nonepidermolytic palmoplantar keratoderma nonpapillary renal cell carcinoma obsolete constipation ophthalmoplegia optic atrophy 1 optic atrophy osteoarthritis osteosarcoma oxyphilic adenoma palmoplantar keratosis panic disorder papillary renal cell carcinoma paraganglioma parathyroid adenoma parathyroid carcinoma pathologic nystagmus peripheral nervous system disease pheochromocytoma phosphorus metabolism disease pilocytic astrocytoma pituitary adenoma placental insufficiency prolactinoma proteinuria protoplasmic astrocytoma ptosis rectal benign neoplasm rectum cancer renal carcinoma renal cell carcinoma renal osteodystrophy retinitis pigmentosa sarcoma sarcomatoid renal cell carcinoma schizophrenia sensorineural hearing loss skin melanoma small intestine benign neoplasm small intestine cancer spindle cell sarcoma spontaneous ocular nystagmus stomach cancer strabismus subependymal giant cell astrocytoma syndromic X-linked intellectual disability 94 type 2 diabetes mellitus ventricular septal defect vesicoureteral reflux visual epilepsy
3312	heat shock protein family A (Hsp70) member 8	HSPA8 Aliases: HSC70 HSC71 HSP73	Homo sapiens (human)
368	ATP binding cassette subfamily C member 6	ABCC6	Homo sapiens (human)

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