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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	July 8, 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 **1851 - 1875** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
60322	carbohydrate sulfotransferase 7	Chst7	Mus musculus (house mouse)
60367	interleukin 1 receptor accessory protein-like 2	Il1rapl2	Mus musculus (house mouse)
60416	phosphofructokinase, platelet	Pfkp	Rattus norvegicus (Norway rat)	disease of metabolism glycogen storage disease
60433	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Rfng	Rattus norvegicus (Norway rat)
60481	ELOVL fatty acid elongase 5	ELOVL5 Aliases: HELO1 dJ483K16.1	Homo sapiens (human)	acute myocardial infarction autosomal dominant cerebellar ataxia cancer cardiac arrest cerebellar ataxia cerebellar disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus embryoma glaucoma glomerulonephritis hyperglycemia kidney disease large intestine cancer low tension glaucoma major depressive disorder melancholic depression myocardial infarction nephritis nephrosis obesity obsolete melancholia pathologic nystagmus primary open angle glaucoma prostate cancer prostate carcinoma pyoureter retinitis pigmentosa 25 schizophrenia silent myocardial infarction spinocerebellar ataxia type 1 spinocerebellar ataxia type 2 spinocerebellar ataxia type 38 spinocerebellar ataxia type 5 spinocerebellar ataxia type 6 spinocerebellar ataxia type 7 spontaneous ocular nystagmus steatotic liver disease type 2 diabetes mellitus
60495	heparanase 2 (inactive)	HPSE2 Aliases: HPA2 HPR2	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 Bloom syndrome Down syndrome Evans' syndrome Glanzmann's thrombasthenia Japanese encephalitis Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune thrombocytopenic purpura bladder carcinoma breast cancer cancer cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma chronic lymphocytic leukemia coronary artery disease coronary thrombosis cribriform carcinoma cryptorchidism dengue disease diabetic ketoacidosis dyskeratosis congenita essential hypertension essential thrombocythemia factor VIII deficiency gestational diabetes gestational trophoblastic neoplasm glaucoma granular cell carcinoma gray platelet syndrome head and neck squamous cell carcinoma hepatitis B hepatitis C hydronephrosis hypertension kidney failure kwashiorkor leiomyoma marasmus migraine multiple myeloma myelodysplastic syndrome myocardial infarction myofibroma nutmeg liver nutrition disease obsolete constipation obsolete type 1 diabetes mellitus 9 ocular hypertension platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 prostate cancer prostate carcinoma protein-energy malnutrition proteinuria qualitative platelet defect silent myocardial infarction squamous cell carcinoma tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus urethral obstruction urinary bladder cancer urinary tract obstruction urofacial syndrome uterine fibroid vesicoureteral reflux viral infectious disease yellow fever
60506	nyctalopin	NYX Aliases: CLRP CSNB1A	Homo sapiens (human)	Balo concentric sclerosis Leber congenital amaurosis 1 Stargardt disease achromatopsia 3 achromatopsia acquired color blindness adrenoleukodystrophy blue color blindness central nervous system disease color blindness cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness 1B congenital stationary night blindness 2A congenital stationary night blindness dissociated nystagmus enhanced S-cone syndrome eye disease fundus albipunctatus hypertropia leukemia mechanical strabismus myopia narcolepsy nervous system disease night blindness ophthalmoplegia pathologic nystagmus red color blindness red-green color blindness retinal disease retinitis pigmentosa retinitis spontaneous ocular nystagmus strabismus
60507	queuine tRNA-ribosyltransferase catalytic subunit 1	Qtrt1	Mus musculus (house mouse)
60666	glycerol-3-phosphate dehydrogenase 1	Gpd1	Rattus norvegicus (Norway rat)
60670	fucosyltransferase 4	Fut4	Rattus norvegicus (Norway rat)	candidiasis
60671	gulonolactone (L-) oxidase	Gulo	Rattus norvegicus (Norway rat)
63827	brevican	BCAN Aliases: BEHAB CSPG7 MGC13038 brevican proteoglycan chondroitin sulfate proteoglycan 7	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 bladder carcinoma central nervous system cancer cerebral degeneration giant cell glioblastoma glioblastoma gliosarcoma high grade glioma middle cerebral artery infarction mixed glioma retinitis pigmentosa urinary bladder cancer
63840	period circadian regulator 2	Per2	Rattus norvegicus (Norway rat)	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
63867	UDP glucuronosyltransferase family 2 member A1	Ugt2a1	Rattus norvegicus (Norway rat)
63888	alpha 1,4-galactosyltransferase	A4galt	Rattus norvegicus (Norway rat)
63917	polypeptide N-acetylgalactosaminyltransferase 11	GALNT11 Aliases: GalNAc-T11 polypeptide GalNAc transferase 11	Homo sapiens (human)	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
64016	queuine tRNA-ribosyltransferase catalytic subunit 1	Qtrt1	Rattus norvegicus (Norway rat)
64035	glycogen phosphorylase L	Pygl	Rattus norvegicus (Norway rat)	glycogen storage disease VI glycogen storage disease lactic acidosis
64043	glucosaminyl (N-acetyl) transferase 1	Gcnt1	Rattus norvegicus (Norway rat)
64064	3-oxoacid CoA-transferase 2	OXCT2 Aliases: FKSG25 FLJ00030 SCOT-T	Homo sapiens (human)
64080	ribokinase	RBKS Aliases: DKFZp686G13268 RBSK	Homo sapiens (human)	bipolar disorder schizophrenia tuberculosis
64083	golgi phosphoprotein 3	GOLPH3 Aliases: GOPP1 GPP34 MIDAS Vps74 coat-protein golgi peripheral membrane protein 1, 34 kDa golgi protein golgi-associated protein	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 Barrett's esophagus Glanzmann's thrombasthenia Hermansky-Pudlak syndrome 2 Japanese encephalitis Lyme disease Pick's disease Reye syndrome X-linked dyskeratosis congenita alternating hemiplegia of childhood anaplastic astrocytoma ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anxiety disorder autonomic neuropathy bladder carcinoma blood coagulation disease breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer carcinoma catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system cancer central nervous system disease cerebral degeneration chikungunya childhood astrocytic tumor childhood cerebral astrocytoma childhood germ cell cancer cholera chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation cystadenoma dengue disease dengue hemorrhagic fever depressive disorder dyskeratosis congenita dysplastic nevus syndrome dysthymic disorder embryoma embryonal cancer endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension fibrillary astrocytoma fibromyalgia gallbladder disease gemistocytic astrocytoma generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma gray platelet syndrome hematopoietic system disease hepatitis A hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension hypochromic anemia hypohidrotic ectodermal dysplasia influenza juvenile pilocytic astrocytoma large intestine cancer liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma major depressive disorder malaria malignant astrocytoma melancholic depression melanoma microphthalmia migraine mixed glioma mucinous adenocarcinoma nervous system disease neuroblastoma neurotic disorder nodular prostate nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete inherited blood coagulation disease obsolete melancholia ovarian cancer ovarian carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma papilloma phobic disorder pilocytic astrocytoma platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma qualitative platelet defect renal carcinoma renal cell carcinoma rhabdomyosarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma spinal stenosis squamous cell papilloma stomach cancer stomach carcinoma subependymal giant cell astrocytoma tongue cancer urinary bladder cancer uterine corpus cancer viral infectious disease yellow fever
64090	galactose-3-O-sulfotransferase 2	GAL3ST2 Aliases: GP3ST	Homo sapiens (human)	Crohn's colitis Crohn's disease ankylosing spondylitis ascending cholangitis cholangitis inflammatory bowel disease 1 inflammatory bowel disease parapsoriasis primary sclerosing cholangitis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole sclerosing cholangitis suppurative cholangitis ulcerative colitis
64096	GDNF family receptor alpha 4	GFRA4 Aliases: persephin receptor	Homo sapiens (human)	Hirschsprung's disease allergic asthma asthma intrinsic asthma multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A panic disorder
64116	solute carrier family 39 member 8	SLC39A8 Aliases: BCG-induced integral membrane protein in monocyte clone 103 BIGM103 Metal cation symporter ZIP8 ZIP-8 ZIP8 ZRT/IRT-like protein 8 Zinc transporter ZIP8	Homo sapiens (human)	Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Leigh disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wilson disease achondroplasia acute chest syndrome alcohol dependence alcohol use disorder alternating hemiplegia of childhood androgen insensitivity syndrome anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy astigmatism atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autonomic neuropathy bacterial sepsis breast cancer breast carcinoma cancer central nervous system disease cerebral infarction cerebrovascular disease childhood leukemia colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ii congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation type IIn congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease craniosynostosis dermatitis diabetes mellitus diabetic ketoacidosis dissociated nystagmus dystonia epilepsy essential hypertension focal hand dystonia generalized dystonia hemochromatosis hydrocephalus hyperopia hypertension hypertropia idiopathic scoliosis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability iron metabolism disease kwashiorkor large intestine cancer learning disability left ventricular noncompaction leukemia macrocytic anemia marasmus mechanical strabismus mitochondrial metabolism disease mitochondrial myopathy nervous system disease neuroblastoma nicotine dependence nutrition disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus protein-energy malnutrition pulmonary tuberculosis schizophrenia sensorineural hearing loss spontaneous ocular nystagmus strabismus systemic lupus erythematosus tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis visual epilepsy

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