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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 **2076 - 2100** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
79888	lysophosphatidylcholine acyltransferase 1	LPCAT1 Aliases: AGPAT10 AGPAT9 FLJ12443 LPLAT8 lysophospholipid acyltransferase 8	Homo sapiens (human)	Leber congenital amaurosis adult respiratory distress syndrome allergic asthma asthma breast cancer breast carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma cancer carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy cystic fibrosis embryoma fundus albipunctatus hepatitis C hepatocellular carcinoma hypereosinophilic syndrome intrinsic asthma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma microglandular adenosis newborn respiratory distress syndrome nonpapillary renal cell carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinitis pigmentosa sarcomatoid renal cell carcinoma sickle cell anemia
79944	L-2-hydroxyglutarate dehydrogenase	L2HGDH Aliases: 2-hydroxyglutarate dehydrogenase FLJ12618	Homo sapiens (human)	2-hydroxyglutaric aciduria D-2-hydroxyglutaric aciduria 1 D-2-hydroxyglutaric aciduria L-2-hydroxyglutaric aciduria brain cancer cerebellar ataxia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital nystagmus disease of metabolism dissociated nystagmus dystonia encephalitis encephalomyelitis epilepsy giant cell glioblastoma glioblastoma hereditary spastic paraplegia high grade glioma hypertropia intellectual disability learning disability mechanical strabismus myelitis nervous system cancer neurodegenerative disease nonpapillary renal cell carcinoma ophthalmoplegia optic atrophy papillary renal cell carcinoma pathologic nystagmus renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 vascular dementia visual epilepsy
79947	dehydrodolichyl diphosphate synthase subunit	DHDDS Aliases: DS FLJ13102 HDS RP59 hCIT	Homo sapiens (human)	Alzheimer's disease Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Dubowitz syndrome Ehrlich tumor carcinoma Laron syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Patau syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome Weissenbacher-Zweymuller syndrome X-linked Aarskog syndrome Zollinger-Ellison syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adult medulloblastoma adult oligodendroglioma agranulocytosis amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bladder carcinoma blepharospasm blindness bone osteosarcoma brain stem glioma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carnitine palmitoyltransferase II deficiency cataract central nervous system cancer central nervous system lymphoma cerebral degeneration cervical squamous cell carcinoma childhood medulloblastoma childhood oligodendroglioma chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congenital diaphragmatic hernia corneal disease cribriform carcinoma cryptorchidism decubitus ulcer dementia depressive disorder developmental delay and seizures with or without movement abnormalities diarrhea dysthymic disorder dystonia early myoclonic encephalopathy embryoma endometrial cancer endometrial carcinoma epilepsy esophagus squamous cell carcinoma focal hand dystonia fundus albipunctatus giant cell glioblastoma glaucoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma hiatus hernia high grade glioma hyperinsulinism hypoglycemia hypogonadism inflammatory bowel disease 1 inflammatory bowel disease islet cell tumor keratoconus kidney failure large intestine cancer leukopenia lingual-facial-buccal dyskinesia liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency mixed glioma mixed oligodendroglioma-astrocytoma multiple myeloma neuroblastoma neurofibromatosis 1 neurofibromatosis neurotic disorder neutropenia obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma oligodendroglioma ophthalmoplegia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic endocrine carcinoma papillary renal cell carcinoma pathological gambling progressive muscular atrophy prostate cancer prostate carcinoma psychotic disorder pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal degeneration retinitis pigmentosa 59 retinitis pigmentosa rippling muscle disease 2 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder severe congenital neutropenia squamous cell carcinoma squamous cell neoplasm status epilepticus steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis substance abuse substance-related disorder thyroid gland medullary carcinoma tooth agenesis tubular adenocarcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer varicocele visual epilepsy
79966	stearoyl-CoA desaturase 5	SCD5 Aliases: ACOD4 FADS4 FLJ21032 HSCD5	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 T-cell acute lymphoblastic leukemia acquired immunodeficiency syndrome age related macular degeneration ankylosing spondylitis arthritis arthropathy autosomal dominant nonsyndromic deafness 79 breast cancer cancer cardiomyopathy cerebral degeneration degeneration of macula and posterior pole depressive disorder diabetes mellitus embryoma endomyocardial fibrosis familial hypertrophic cardiomyopathy hepatocellular carcinoma human immunodeficiency virus infectious disease hypertrophic cardiomyopathy liver cancer macular degeneration melanoma osteoarthritis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary immunodeficiency disease restrictive cardiomyopathy rheumatoid arthritis sickle cell anemia skin melanoma systemic lupus erythematosus systemic primary carnitine deficiency disease type 2 diabetes mellitus
79993	ELOVL fatty acid elongase 7	ELOVL7 Aliases: FLJ23563	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy cancer hidradenitis suppurativa hidradenitis inflammatory bowel disease multiple system atrophy pompholyx prostate cancer prostate carcinoma
80055	post-GPI attachment to proteins inositol deacylase 1	PGAP1 Aliases: Bst1 FLJ12377 GPI inositol-deacylase SPG67	Homo sapiens (human)	Burkitt lymphoma Laron syndrome achondroplasia agnosia autosomal recessive intellectual developmental disorder brain disease cerebral degeneration choreatic disease congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy factor XII deficiency focal epilepsy fundus dystrophy holoprosencephaly 1 holoprosencephaly intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia paroxysmal nocturnal hemoglobinuria partial motor epilepsy stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
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
80146	UDP-glucuronate decarboxylase 1	UXS1 Aliases: FLJ23591 SDR6E1 UGD short chain dehydrogenase/reductase family 6E, member 12	Homo sapiens (human)	bipolar disorder hereditary multiple exostoses schizoaffective disorder schizophrenia schizophreniform disorder
80162	protein-glucosylgalactosylhydroxylysine glucosidase	PGGHG Aliases: FLJ22635	Homo sapiens (human)
80168	monoacylglycerol O-acyltransferase 2	MOGAT2 Aliases: DGAT2L5 FLJ22644 MGAT2	Homo sapiens (human)	diabetes mellitus diabetic ketoacidosis disease of metabolism glucose intolerance hepatocellular carcinoma liver cancer prediabetes syndrome type 2 diabetes mellitus
80201	hexokinase domain containing 1	HKDC1 Aliases: FLJ22761 FLJ37767	Homo sapiens (human)	breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer colorectal cancer colorectal carcinoma cone-rod dystrophy corneal disease embryoma fundus albipunctatus gestational diabetes glucose metabolism disease hepatitis hyperglycemia hyperinsulinemic hypoglycemia keratoconus large intestine cancer late-onset retinal degeneration lung benign neoplasm lung cancer lung carcinoma maturity-onset diabetes of the young retinitis pigmentosa steatotic liver disease
80235	phosphatidylinositol glycan anchor biosynthesis class Z	PIGZ Aliases: FLJ12768 GPI mannosyltransferase 4 GPI-MT-IV MGC52163 PIG-Z SMP3 SMP3 homolog (S. cerevisiae) dol-P-Man dependent GPI mannosyltransferase hSMP3	Homo sapiens (human)	cancer visceral leishmaniasis
80255	solute carrier family 35 member F5	SLC35F5 Aliases: FLJ22004	Homo sapiens (human)	Kawasaki disease cancer
80267	ER degradation enhancing alpha-mannosidase like protein 3	EDEM3	Homo sapiens (human)	congenital disorder of glycosylation type II hepatitis C prostate cancer prostate carcinoma
80270	hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7	HSD3B7 Aliases: C(27)-3BETA-HSD SDR11E3 short chain dehydrogenase/reductase family 11E, member 3	Homo sapiens (human)	Gilbert syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease bilirubin metabolic disorder blood coagulation disease cancer cholestasis congenital bile acid synthesis defect 1 congenital bile acid synthesis defect congenital stationary night blindness 1A congenital stationary night blindness diarrhea gallbladder disease giant cell glioblastoma glioblastoma high grade glioma intrahepatic cholestasis liver disease neuropathy night blindness obsolete inherited blood coagulation disease obsolete steatorrhea osteomalacia osteoporosis peripheral nervous system disease progressive familial intrahepatic cholestasis 1 progressive familial intrahepatic cholestasis 4 progressive familial intrahepatic cholestasis rickets tropical sprue
80271	inositol-trisphosphate 3-kinase C	ITPKC Aliases: IP3-3KC IP3KC	Homo sapiens (human)	Hirschsprung's disease Kawasaki disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma colorectal cancer coronary aneurysm nephrolithiasis uric acid nephrolithiasis
80285	poly (ADP-ribose) polymerase family, member 9	Parp9	Mus musculus (house mouse)
80294	protein O-fucosyltransferase 2	Pofut2	Mus musculus (house mouse)	Down syndrome
80328	UL16 binding protein 2	ULBP2 Aliases: RAET1H	Homo sapiens (human)	acute myeloid leukemia bone osteosarcoma cancer childhood leukemia childhood osteosarcoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer embryoma familial retinoblastoma large intestine cancer multiple myeloma osteosarcoma pancreatic cancer pancreatic carcinoma retinoblastoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma trilateral retinoblastoma
80329	UL16 binding protein 1	ULBP1 Aliases: RAET1I	Homo sapiens (human)	Crohn's colitis Crohn's disease Kawasaki disease adult lymphoma bone osteosarcoma bronchus cancer bronchus carcinoma cancer embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis C hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma osteosarcoma stomach cancer stomach carcinoma ulcerative colitis
80339	patatin like phospholipase domain containing 3	PNPLA3 Aliases: FLJ22012 adiponutrin dJ796I17.1 iPLA2epsilon	Homo sapiens (human)	Chanarin-Dorfman syndrome Phelan-McDermid syndrome Wernicke-Korsakoff syndrome Wilson disease Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acquired metabolic disease acute lymphoblastic leukemia adrenoleukodystrophy adult hepatocellular carcinoma adult liposarcoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis bipolar disorder cancer cardiovascular system disease carotid artery disease celiac disease childhood hepatocellular carcinoma childhood liposarcoma cholecystolithiasis choledocholithiasis cholelithiasis chronic kidney disease congenital hypothyroidism coronary artery disease diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma familial hyperlipidemia gallbladder disease gestational diabetes glucose intolerance heart disease hemochromatosis type 1 hemochromatosis hepatitis B hepatitis C hepatitis hepatocellular carcinoma human immunodeficiency virus infectious disease hyperglycemia hyperinsulinism hypertrophic cardiomyopathy 1 hypothyroidism inflammatory bowel disease intrahepatic cholestasis of pregnancy intrinsic asthma iron metabolism disease kidney failure liposarcoma liver cancer liver carcinoma liver cirrhosis liver disease lymphoblastic lymphoma metabolic dysfunction-associated steatotic liver disease mood disorder morbid obesity myxedema obesity obsolete type 1 diabetes mellitus 9 osteoarthritis pleomorphic liposarcoma polycystic ovary syndrome portal hypertension prediabetes syndrome premenstrual tension primary biliary cholangitis primary sclerosing cholangitis sclerosing cholangitis steatotic liver disease 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 type 2 diabetes mellitus viral infectious disease
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
80723	solute carrier family 35 member G2	SLC35G2 Aliases: DKFZp564K2464 MGC3295	Homo sapiens (human)	chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
80772	ceramide-1-phosphate transfer protein	CPTP Aliases: MGC10334	Homo sapiens (human)	acute pancreatitis pancreatitis
80881	stress-associated endoplasmic reticulum protein 1	Serp1	Rattus norvegicus (Norway rat)

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