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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 **1001 - 1025** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
57798	GATA zinc finger domain containing 1	GATAD1	Homo sapiens (human)
10523	calcium homeostasis endoplasmic reticulum protein	CHERP	Homo sapiens (human)
115350	Fc receptor like 1	FCRL1	Homo sapiens (human)
7739	zinc finger protein 185 with LIM domain	ZNF185	Homo sapiens (human)
9448	mitogen-activated protein kinase kinase kinase kinase 4	MAP4K4	Homo sapiens (human)
285852	triggering receptor expressed on myeloid cells like 4	TREML4	Homo sapiens (human)
57223	protein phosphatase 4 regulatory subunit 3B	PPP4R3B	Homo sapiens (human)
8936	WASP family member 1	WASF1	Homo sapiens (human)
4593	muscle associated receptor tyrosine kinase	MUSK	Homo sapiens (human)
5870	RAB6A, member RAS oncogene family	RAB6A	Homo sapiens (human)
57643	zinc finger SWIM-type containing 5	ZSWIM5	Homo sapiens (human)
619279	zinc finger protein 704	ZNF704	Homo sapiens (human)
18	4-aminobutyrate aminotransferase	ABAT Aliases: 4-aminobutyrate transaminase GABA transaminase GABA-T GABAT gamma-aminobutyrate aminotransferase	Homo sapiens (human)	Alzheimer's disease GABA aminotransferase deficiency Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lennox-Gastaut syndrome Parkinsonism Pick's disease West syndrome alcohol dependence alcohol use disorder amnestic disorder anxiety disorder arthritis arthropathy autism spectrum disorder autistic disorder cancer cocaine abuse cocaine dependence depressive disorder dissociative amnesia embryoma epilepsy esophagitis essential hypertension essential thrombocythemia focal epilepsy gastroesophageal reflux disease hematologic cancer heroin dependence hypertension ischemia leukodystrophy major depressive disorder mood disorder morphine dependence myelodysplastic syndrome neurotic disorder obsolete infantile epileptic encephalopathy opiate dependence osteoarthritis partial motor epilepsy peptic esophagitis phobic disorder recurrent hypersomnia reflex epilepsy secondary Parkinson disease status epilepticus substance abuse substance-related disorder visual epilepsy
8200	growth differentiation factor 5	GDF5	Homo sapiens (human)
221092	heterogeneous nuclear ribonucleoprotein U like 2	HNRNPUL2	Homo sapiens (human)
57704	glucosylceramidase beta 2	GBA2 Aliases: AD035 DKFZp762K054 KIAA1605 bile acid beta-glucosidase glucocerebrosidase 2 non-lysosomal glucosylceramidase	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 Gaucher's disease Henoch-Schoenlein purpura Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease SPOAN syndrome Troyer syndrome alternating hemiplegia of childhood autonomic neuropathy cancer cataract central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration congenital nystagmus cystic fibrosis dementia dissociated nystagmus glaucoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hypersensitivity vasculitis infertility intellectual disability learning disability male infertility nervous system disease paraplegia pathologic nystagmus scoliosis sensorineural hearing loss spontaneous ocular nystagmus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
79414	leucine rich repeat and fibronectin type III domain containing 3	LRFN3	Homo sapiens (human)
138881	olfactory receptor family 1 subfamily L member 8	OR1L8	Homo sapiens (human)
3265	HRas proto-oncogene, GTPase	HRAS	Homo sapiens (human)
1374	carnitine palmitoyltransferase 1A	CPT1A Aliases: CPT1-L L-CPT1	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 D-bifunctional protein deficiency Niemann-Pick disease type C1 Niemann-Pick disease Pearson syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction alcoholic hepatitis alveolar rhabdomyosarcoma amnestic disorder beta thalassemia breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency cataract 4 multiple types cerebral degeneration chronic fatigue syndrome chronic kidney disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential thrombocythemia familial hyperlipidemia familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease isolated elevated serum creatine phosphokinase levels large intestine cancer lipid metabolism disorder liver cancer liver carcinoma liver cirrhosis lymphangioleiomyomatosis major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma metabolic dysfunction-associated steatohepatitis mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction nasopharynx carcinoma neurotic disorder obesity obsolete melancholia osteoporosis placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis renal tubular acidosis retrograde amnesia sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction skin melanoma speech disorder steatotic liver disease stomach cancer stomach carcinoma sudden infant death syndrome systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency visual epilepsy
81399	olfactory receptor family 4 subfamily F member 16	OR4F16	Homo sapiens (human)
54623	PAF1 homolog, Paf1/RNA polymerase II complex component	PAF1	Homo sapiens (human)
26059	ELKS/RAB6-interacting/CAST family member 2	ERC2	Homo sapiens (human)
56667	mucin 13, cell surface associated	MUC13	Homo sapiens (human)
92737	delta/notch like EGF repeat containing	DNER	Homo sapiens (human)

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