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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 **7901 - 7925** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
717	complement C2	C2	Homo sapiens (human)
29109	formin homology 2 domain containing 1	FHOD1	Homo sapiens (human)
55752	septin 11	SEPTIN11	Homo sapiens (human)
653275	cryptic, EGF-CFC family member 1B	CFC1B	Homo sapiens (human)
3037	hyaluronan synthase 2	HAS2	Homo sapiens (human)	Barrett's esophagus Down syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma allergic asthma anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer childhood cerebral astrocytoma childhood osteosarcoma chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congenital heart disease coronary artery disease cribriform carcinoma diabetes insipidus diabetes mellitus diabetic ketoacidosis embryoma endocrine exophthalmos enophthalmos essential thrombocythemia fibrillary astrocytoma gemistocytic astrocytoma gliosarcoma glomerulonephritis granular cell carcinoma high grade glioma hyperglycemia hyperuricemia idiopathic interstitial pneumonia intrinsic asthma juvenile pilocytic astrocytoma kidney disease large intestine cancer leukoencephalopathy with vanishing white matter liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacytic lymphoma macroglobulinemia malignant astrocytoma melanoma microphthalmia middle cerebral artery infarction mixed glioma multiple myeloma myelodysplastic syndrome myopia myotonic dystrophy type 1 nephritis nephrosis neurohypophyseal diabetes insipidus obesity obsolete Matthew-Wood syndrome obsolete exophthalmos obsolete lymphoplasmacytic lymphoma orbital disease osteosarcoma pilocytic astrocytoma placental insufficiency polycystic ovary syndrome postinflammatory pulmonary fibrosis primary open angle glaucoma primary pulmonary hypertension protoplasmic astrocytoma pulmonary fibrosis pulmonary hypertension pyoureter sarcomatoid carcinoma skin melanoma squamous cell carcinoma subependymal giant cell astrocytoma tetralogy of Fallot tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer ventricular septal defect
56262	leucine rich repeat containing 8 VRAC subunit A	LRRC8A	Homo sapiens (human)
30816	endogenous retrovirus group W member 1, envelope	ERVW-1	Homo sapiens (human)
10257	ATP binding cassette subfamily C member 4 (PEL blood group)	ABCC4	Homo sapiens (human)
164592	coiled-coil domain containing 116	CCDC116	Homo sapiens (human)
4646	myosin VI	MYO6	Homo sapiens (human)
56245	exosomal polycystin 1 interacting protein	EPCIP	Homo sapiens (human)
2897	glutamate ionotropic receptor kainate type subunit 1	GRIK1	Homo sapiens (human)
9869	SET domain bifurcated histone lysine methyltransferase 1	SETDB1	Homo sapiens (human)
374395	transmembrane protein 179B	TMEM179B	Homo sapiens (human)
7073	TIA1 cytotoxic granule associated RNA binding protein like 1	TIAL1	Homo sapiens (human)
91949	component of oligomeric golgi complex 7	COG7	Homo sapiens (human)	Cauda equina syndrome Laron syndrome achondroplasia autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis cardiomyopathy cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIe congenital disorder of glycosylation congenital heart disease congestive heart failure endomyocardial fibrosis esophagitis familial hypertrophic cardiomyopathy gastroesophageal reflux disease genetic disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels microcephaly neurogenic bladder obsolete congenital ichthyosiform erythroderma peptic esophagitis placental insufficiency sensorineural hearing loss
1968	eukaryotic translation initiation factor 2 subunit gamma	EIF2S3 Aliases: EIF2 EIF2gamma eukaryotic translation initiation factor 2G	Homo sapiens (human)
91373	UDP-N-acetylglucosamine pyrophosphorylase 1 like 1	UAP1L1	Homo sapiens (human)	hepatocellular carcinoma liver cancer
63877	family with sequence similarity 204 member A	FAM204A	Homo sapiens (human)
5836	glycogen phosphorylase L	PYGL Aliases: GSD6 Hers disease glycogen phosphorylase, liver form glycogen storage disease type VI	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome achondroplasia cystinuria galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease III glycogen storage disease IV glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease hepatocellular carcinoma hypoglycemia lactic acidosis liver cancer
134864	trace amine associated receptor 1	TAAR1	Homo sapiens (human)
2747	glutamate dehydrogenase 2	GLUD2	Homo sapiens (human)
55035	nucleolar protein 8	NOL8	Homo sapiens (human)
84866	transmembrane protein 25	TMEM25	Homo sapiens (human)
5648	MBL associated serine protease 1	MASP1 Aliases: C4/C2 activating component of Ra-reactive factor MAP-1 MASP MASP-3 Map44 mannose-binding lectin-associated serine protease 1	Homo sapiens (human)	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC syndrome 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 Bloch-Sulzberger syndrome Klippel-Feil syndrome Lewy body dementia Marfan syndrome Pick's disease Reye syndrome acute myocardial infarction age related macular degeneration amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 6 arthritis arthropathy 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 atypical hemolytic-uremic syndrome bacterial infectious disease bacterial sepsis blepharophimosis blindness cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cleft lip cleft palate cleidocranial dysplasia congenital ptosis coronary thrombosis craniosynostosis cryptorchidism cystic fibrosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis disseminated intravascular coagulation esophagus squamous cell carcinoma gallbladder disease glaucoma glomerulonephritis heart disease hemolytic-uremic syndrome hepatitis C humeroradial synostosis hydronephrosis hypomelanosis of Ito inclusion body myopathy with Paget disease of bone and frontotemporal dementia inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 intellectual disability isolated cleft palate kidney disease kidney failure learning disability liver cirrhosis liver disease lung squamous cell carcinoma lupus erythematosus macular degeneration microcephaly multiple sclerosis myocardial infarction nephritis omphalocele patent ductus arteriosus patent foramen ovale placental insufficiency prostate cancer prostate carcinoma ptosis pulmonary tuberculosis purpura fulminans radioulnar synostosis rheumatoid arthritis scoliosis sensorineural hearing loss silent myocardial infarction situs inversus spina bifida occulta spondylolisthesis squamous cell carcinoma systemic lupus erythematosus tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tuberous sclerosis type 2 diabetes mellitus umbilical hernia uremia vascular dementia ventricular septal defect

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