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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 **7126 - 7150** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
80221	acyl-CoA synthetase family member 2	ACSF2	Homo sapiens (human)
314	amine oxidase copper containing 2	AOC2	Homo sapiens (human)
93432	maltase-glucoamylase 2 (putative)	MGAM2	Homo sapiens (human)
51227	phosphatidylinositol glycan anchor biosynthesis class P	PIGP Aliases: DCRC DSRC phosphatidylinositol-n-acetylglucosaminyltranferase subunit P	Homo sapiens (human)	Down syndrome Joubert syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Unverricht-Lundborg syndrome West syndrome aromatase excess syndrome basal ganglia disease blepharospasm cleft palate complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 55 dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy epilepsy episodic ataxia focal hand dystonia hydranencephaly hypertropia intellectual disability isolated cleft palate learning disability lingual-facial-buccal dyskinesia lissencephaly mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 prostate cancer prostate carcinoma renal agenesis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus strabismus syndromic X-linked intellectual disability Najm type tuberous sclerosis umbilical hernia ureterocele ventricular septal defect visual cortex disease visual epilepsy
219453	olfactory receptor family 8 subfamily K member 5	OR8K5	Homo sapiens (human)
8728	ADAM metallopeptidase domain 19	ADAM19	Homo sapiens (human)
6916	thromboxane A synthase 1	TBXAS1 Aliases: CYP5 CYP5A1 THAS TS TXAS TXS cytochrome P450, family 5, subfamily A, polypeptide 1	Homo sapiens (human)	Camurati-Engelmann disease Ghosal hematodiaphyseal syndrome acute myocardial infarction acute necrotizing pancreatitis alcoholic hepatitis alcoholic liver cirrhosis allergic asthma anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma ataxia telangiectasia atherosclerosis autosomal recessive osteopetrosis 7 benign mesothelioma brain infarction brain stem infarction breast cancer breast carcinoma cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis essential hypertension glomerulonephritis heart disease hydronephrosis hypertension inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease liver cirrhosis lung benign neoplasm macrocytic anemia malignant mesothelioma malignant pleural mesothelioma membranous glomerulonephritis myelofibrosis myocardial infarction nephritis osteopetrosis osteosclerosis pancytopenia pituitary adenoma pituitary cancer pituitary carcinoma platelet-type bleeding disorder 14 prostate cancer prostate carcinoma pulmonary embolism schizophrenia silent myocardial infarction speech disorder thrombocytopenia thrombosis ulcerative colitis urinary bladder cancer
9699	regulating synaptic membrane exocytosis 2	RIMS2	Homo sapiens (human)
223	aldehyde dehydrogenase 9 family member A1	ALDH9A1 Aliases: E3	Homo sapiens (human)	cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hemolytic anemia kidney cancer nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
126	alcohol dehydrogenase 1C (class I), gamma polypeptide	ADH1C	Homo sapiens (human)	Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adrenoleukodystrophy adult hepatocellular carcinoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis anaplastic astrocytoma arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant hypocalcemia 1 autosomal dominant hypocalcemia bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiovascular system disease cerebellar ataxia, mental retardation and dysequlibrium syndrome cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood cerebral astrocytoma childhood hepatocellular carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart coronary artery disease coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis fibrillary astrocytoma follicular adenoma gallbladder disease gemistocytic astrocytoma glucose intolerance granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemorrhoid hepatocellular carcinoma high grade glioma islet cell tumor juvenile pilocytic astrocytoma large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer late onset Parkinson's disease liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder malignant astrocytoma melancholic depression microcystic adenoma myocardial infarction neurotic disorder nicotine dependence nutmeg liver obsolete constipation obsolete melancholia oropharynx cancer pancreatic cancer pancreatic carcinoma pancreatitis papillary adenoma pharynx cancer pilocytic astrocytoma prediabetes syndrome prostate cancer prostate carcinoma protoplasmic astrocytoma secondary Parkinson disease silent myocardial infarction situs inversus squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tongue squamous cell carcinoma tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer
2916	glutamate metabotropic receptor 6	GRM6	Homo sapiens (human)
339977	leucine rich repeat containing 66	LRRC66	Homo sapiens (human)
10395	DLC1 Rho GTPase activating protein	DLC1	Homo sapiens (human)
79812	multimerin 2	MMRN2	Homo sapiens (human)
5024	purinergic receptor P2X 3	P2RX3	Homo sapiens (human)
57134	mannosidase alpha class 1C member 1	MAN1C1 Aliases: HMIC	Homo sapiens (human)	cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma nonpapillary renal cell carcinoma papillary renal cell carcinoma pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
4126	mannosidase beta	MANBA Aliases: beta-mannosidase A	Homo sapiens (human)	Fabry disease allergic asthma allergic disease alternating hemiplegia of childhood angiokeratoma ascending cholangitis asthma attention deficit hyperactivity disorder autonomic neuropathy beta-mannosidosis central nervous system disease cholangitis chronic kidney disease chylomicron retention disease colorectal cancer colorectal carcinoma complement deficiency congenital nystagmus dissociated nystagmus epilepsy intellectual disability intrinsic asthma large intestine cancer learning disability lipid storage disease lysosomal storage disease multiple sclerosis nervous system disease obsolete constipation pathologic nystagmus primary biliary cholangitis primary sclerosing cholangitis sarcoidosis sclerosing cholangitis sensorineural hearing loss speech disorder spontaneous ocular nystagmus suppurative cholangitis uveoparotid fever visual epilepsy
5965	RecQ like helicase	RECQL	Homo sapiens (human)
253943	YTH N6-methyladenosine RNA binding protein F3	YTHDF3	Homo sapiens (human)
9586	cAMP responsive element binding protein 5	CREB5	Homo sapiens (human)
23286	WW and C2 domain containing 1	WWC1	Homo sapiens (human)
80142	prostaglandin E synthase 2	PTGES2 Aliases: FLJ14038	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 Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 adenocarcinoma adenoma cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma diabetes mellitus endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma essential hypertension glucose intolerance granular cell carcinoma hypertension large intestine cancer obesity periodontitis prediabetes syndrome prostate cancer prostate carcinoma thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma tubular adenocarcinoma type 2 diabetes mellitus type C thymoma uterine corpus cancer
55361	phosphatidylinositol 4-kinase type 2 alpha	PI4K2A Aliases: DKFZP761G1923 PI4KII PIK42A	Homo sapiens (human)	Hermansky-Pudlak syndrome breast cancer cancer embryoma giant cell glioblastoma glioblastoma
84803	glycerol-3-phosphate acyltransferase 3	GPAT3 Aliases: AGPAT10 HMFN0839 LPAAT-theta MAG1 MGC11324 lysophosphatidic acid acyltransferase, theta	Homo sapiens (human)	acquired immunodeficiency syndrome acute myeloid leukemia breast cancer cancer endometritis human immunodeficiency virus infectious disease leech infestation myiasis obesity toxoplasmosis
3820	killer cell lectin like receptor B1	KLRB1 Aliases: CD161 CLEC5B NKR-P1 NKR-P1A hNKR-P1A natural killer cell surface protein P1A	Homo sapiens (human)	Goodpasture syndrome Takayasu's arteritis acquired immunodeficiency syndrome acute promyelocytic leukemia aggressive NK-cell leukemia allergic asthma arthritis arthropathy asthma autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bone disease bronchus cancer bronchus carcinoma cancer cartilage disease cataract connective tissue disease eclampsia embryoma familial multiple nevi flammei granulomatosis with polyangiitis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hidradenitis suppurativa hidradenitis human immunodeficiency virus infectious disease immune system disease influenza intermittent claudication intrinsic asthma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 melanoma mitral valve stenosis multiple myeloma multiple sclerosis myocarditis osteoarthritis peeling skin syndrome periodontitis placental insufficiency pneumonia polyarteritis nodosa pompholyx prostate cancer prostate carcinoma psoriatic arthritis rheumatoid arthritis scleroderma skin melanoma spondyloarthropathy spondylosis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tuberculosis urinary bladder cancer viral infectious disease

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