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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 **1901 - 1925** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
9526	mannose-P-dolichol utilization defect 1	MPDU1 Aliases: CDGIf Lec35 PQLC5 SL15 SLC66A5	Homo sapiens (human)	IgA glomerulonephritis acquired hyperkeratosis autosomal recessive congenital ichthyosis 1 blindness cancer cerebral degeneration congenital disorder of glycosylation Id congenital disorder of glycosylation If congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism congenital nystagmus craniosynostosis cystinuria dissociated nystagmus galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hypertropia hypothyroidism ichthyosis keratosis follicularis mechanical strabismus microcephaly mongolian spot myxedema obsolete congenital ichthyosiform erythroderma ophthalmoplegia optic atrophy pathologic nystagmus pseudoxanthoma elasticum spontaneous ocular nystagmus strabismus
29071	C1GALT1 specific chaperone 1	C1GALT1C1 Aliases: C1GALT2 COSMC	Homo sapiens (human)	IgA glomerulonephritis Tn polyagglutination syndrome angioma serpiginosum autoimmune disease autoimmune lymphoproliferative syndrome cancer capillary hemangioma cavernous hemangioma chorioangioma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma endometrial cancer endometrial carcinoma glomerulonephritis glomus tumor hemangioma hemolytic-uremic syndrome hepatocellular carcinoma histiocytoid hemangioma immune system disease inflammatory bowel disease intramuscular hemangioma kidney disease large intestine cancer liver cancer lymphangioma microphthalmia nephritis nephrosis obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma pyoureter uterine corpus cancer vitiligo
22908	SAC1 like phosphatidylinositide phosphatase	SACM1L Aliases: KIAA0851 SAC1	Homo sapiens (human)	IgA glomerulonephritis T-cell acute lymphoblastic leukemia acute lymphoblastic leukemia adult T-cell leukemia/lymphoma brain infarction breast cancer carotid artery thrombosis carotid stenosis cerebral infarction cerebrovascular disease coronary artery disease diabetes mellitus diabetic ketoacidosis epilepsy essential hypertension glomerulonephritis hemophilia B hypertension kidney disease lymphoblastic lymphoma maturity-onset diabetes of the young nephritis nephrosis obsolete T-cell lymphoblastic leukemia/lymphoma pyoureter rheumatoid arthritis type 2 diabetes mellitus visual epilepsy von Willebrand's disease 3 von Willebrand's disease
22925	phospholipase A2 receptor 1	PLA2R1 Aliases: CLEC13C PLA2-R PLA2G1R PLA2IR	Homo sapiens (human)	IgA glomerulonephritis T-cell acute lymphoblastic leukemia Werner syndrome acute biphenotypic leukemia acute leukemia acute myeloid leukemia adrenoleukodystrophy allergic asthma asthma autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer cardiac arrest childhood leukemia chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma collecting duct carcinoma embryoma essential thrombocythemia familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease interstitial nephritis intrinsic asthma kidney cancer kidney disease leukemia lipoid nephrosis lupus erythematosus lupus nephritis membranous glomerulonephritis myelodysplastic syndrome nephritis nephrosis nephrotic syndrome nonpapillary renal cell carcinoma papillary renal cell carcinoma progeria prostate cancer prostate carcinoma pyelitis pyelonephritis pyoureter renal carcinoma renal cell carcinoma renal infectious disease sarcomatoid renal cell carcinoma substance abuse substance-related disorder systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma
6519	solute carrier family 3 member 1	SLC3A1 Aliases: ATR1 CSNU1 D2H NBAT RBAT amino acid transporter 1 neutral and basic amino acid transport protein rBAT	Homo sapiens (human)	IgA glomerulonephritis Marfan syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy breast cancer breast carcinoma bulimia nervosa calcinosis calcium metabolism disease cancer chronic kidney disease colon carcinoma colorectal cancer congenital myasthenic syndrome 22 congenital ptosis coronary thrombosis cystinuria diabetes mellitus diabetic ketoacidosis distal myopathy epilepsy essential hypertension facioscapulohumeral muscular dystrophy galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease high grade glioma hypercalcemia hypertension hypoglycemia hypogonadism hypotonia-cystinuria syndrome interstitial nephritis kidney failure lactic acidosis limb-girdle muscular dystrophy muscular dystrophy myocardial infarction nephrocalcinosis nephrolithiasis nephrosclerosis obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy panic disorder phosphorus metabolism disease primary pulmonary hypertension prostate cancer prostate carcinoma ptosis pyelitis pyelonephritis renal hypertension renal infectious disease silent myocardial infarction situs inversus synovial sarcoma tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis urinary tract obstruction vesicoureteral reflux visual epilepsy
4125	mannosidase alpha class 2B member 1	MAN2B1 Aliases: LAMAN lysosomal alpha-mannosidase	Homo sapiens (human)	IgA glomerulonephritis Klippel-Feil syndrome age related macular degeneration alpha-mannosidosis aspartylglucosaminuria cerebral degeneration congenital nystagmus degeneration of macula and posterior pole dissociated nystagmus fucosidosis gingival hypertrophy gingival overgrowth glycogen storage disease II hypertrichosis inguinal hernia intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease macular degeneration methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis pathologic nystagmus retinal degeneration sensorineural hearing loss spondylolisthesis spontaneous ocular nystagmus
6296	acyl-CoA synthetase medium chain family member 3	ACSM3 Aliases: SA	Homo sapiens (human)	IgA glomerulonephritis Kallmann syndrome Marfan syndrome Sheehan syndrome abdominal obesity-metabolic syndrome 1 anemia autism spectrum disorder autistic disorder bacterial sepsis brain cancer brain stem infarction breast cancer breast carcinoma cancer cardiovascular system disease cataract cerebral artery occlusion cerebral infarction cerebrovascular disease chronic kidney disease communicating hydrocephalus diabetes mellitus diabetic ketoacidosis embryoma epilepsy essential hypertension essential thrombocythemia generalized atherosclerosis heart disease hemosiderosis hepatocellular carcinoma hereditary coproporphyria hydrocephalus hyperglycemia hypertension hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic scoliosis intracranial aneurysm intracranial vasospasm isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency liver cancer liver carcinoma macrocytic anemia obesity obstructive hydrocephalus ocular hypertension oculomotor nerve paralysis panhypopituitarism partial third-nerve palsy post-traumatic stress disorder prostate cancer prostate carcinoma senile degeneration of brain sensorineural hearing loss situs inversus tetralogy of Fallot thrombophilia thymus gland disease total third-nerve palsy transient cerebral ischemia tuberous sclerosis ulcerative colitis visual epilepsy
257202	glutathione peroxidase 6	GPX6 Aliases: selenoprotein GPX6	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease breast cancer depressive disorder lung squamous cell carcinoma major depressive disorder melancholic depression obsolete melancholia ovarian cancer ovarian carcinoma
23475	quinolinate phosphoribosyltransferase	QPRT Aliases: QPRTase nicotinate-nucleotide pyrophosphorylase (carboxylating)	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease acute myeloid leukemia adenoma adenosarcoma endemic goiter follicular adenoma gliosarcoma hepatitis C high grade glioma microcystic adenoma mixed glioma nephroblastoma neuroblastoma neurodegenerative disease papillary adenoma substernal goiter thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma
8526	diacylglycerol kinase epsilon	DGKE Aliases: DAGK6 DGK	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease acute kidney failure allergic asthma asthma atypical hemolytic-uremic syndrome breast cancer cancer capillary disease cardiovascular system disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy embryoma epilepsy familial nephrotic syndrome fundus albipunctatus glomerulonephritis heart disease hemolytic anemia hemolytic-uremic syndrome hereditary hemorrhagic telangiectasia intrinsic asthma kidney disease kidney failure large intestine cancer lipoid nephrosis liver cirrhosis membranoproliferative glomerulonephritis mitochondrial DNA depletion syndrome nephritis nephrosis nephrotic syndrome type 7 nephrotic syndrome obesity proteinuria pyoureter retinitis pigmentosa telangiectasis thrombocytopenia thrombotic thrombocytopenic purpura uremia visual epilepsy
2997	glycogen synthase 1	GYS1 Aliases: GSY	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lafora disease abdominal obesity-metabolic syndrome 1 acute myocardial infarction arthritis arthropathy cardiomyopathy cardiovascular system disease coronary thrombosis diabetes mellitus diabetic ketoacidosis endomyocardial fibrosis essential thrombocythemia hypertrophic cardiomyopathy hypoglycemia myelodysplastic syndrome myocardial infarction obsolete type 1 diabetes mellitus 9 rheumatoid arthritis silent myocardial infarction 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 visual epilepsy
850608	nicotinate-nucleotide diphosphorylase (carboxylating)	BNA6	Saccharomyces cerevisiae S288C	Huntington's disease
67375	quinolinate phosphoribosyltransferase	Qprt	Mus musculus (house mouse)	Huntington's disease
293504	quinolinate phosphoribosyltransferase	Qprt	Rattus norvegicus (Norway rat)	Huntington's disease
7351	uncoupling protein 2	UCP2	Homo sapiens (human)	Huntington's disease carotid artery disease congestive heart failure diabetic neuropathy end stage renal disease hypertension hypothyroidism metabolic dysfunction-associated steatotic liver disease obesity obstructive jaundice polycystic liver disease steatotic liver disease transient cerebral ischemia type 2 diabetes mellitus
54315	uncoupling protein 2	Ucp2	Rattus norvegicus (Norway rat)	Huntington's disease carotid artery disease congestive heart failure diabetic neuropathy end stage renal disease hypertension hypothyroidism metabolic dysfunction-associated steatotic liver disease obesity obstructive jaundice polycystic liver disease steatotic liver disease transient cerebral ischemia type 2 diabetes mellitus
22228	uncoupling protein 2 (mitochondrial, proton carrier)	Ucp2	Mus musculus (house mouse)	Huntington's disease carotid artery disease congestive heart failure diabetic neuropathy end stage renal disease hypertension hypothyroidism metabolic dysfunction-associated steatotic liver disease obesity obstructive jaundice polycystic liver disease steatotic liver disease transient cerebral ischemia type 2 diabetes mellitus
105787	protein kinase, AMP-activated, alpha 1 catalytic subunit	Prkaa1	Mus musculus (house mouse)	Huntington's disease Parkinson's disease breast cancer cholestasis colon cancer lung non-small cell carcinoma obesity type 2 diabetes mellitus
65248	protein kinase AMP-activated catalytic subunit alpha 1	Prkaa1	Rattus norvegicus (Norway rat)	Huntington's disease Parkinson's disease breast cancer cholestasis colon cancer lung non-small cell carcinoma obesity type 2 diabetes mellitus
5562	protein kinase AMP-activated catalytic subunit alpha 1	PRKAA1	Homo sapiens (human)	Huntington's disease Parkinson's disease breast cancer cholestasis colon cancer lung non-small cell carcinoma obesity type 2 diabetes mellitus
37447	Syndecan	Sdc	Drosophila melanogaster (fruit fly)	Hodgkin's lymphoma bacterial infectious disease cleft lip cleft palate familial hyperlipidemia hyperglycemia lung adenocarcinoma myocardial infarction obesity proteinuria type 2 diabetes mellitus
22927	hyaluronan binding protein 4	HABP4 Aliases: IHABP4 SERBP1L	Homo sapiens (human)	Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma
4065	lymphocyte antigen 75	LY75 Aliases: CD205 CLEC13B DEC-205	Homo sapiens (human)	Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma breast cancer breast carcinoma cancer carcinoma cholesteatoma chronic fatigue syndrome congestive heart failure diabetes mellitus dilated cardiomyopathy 1A dilated cardiomyopathy embryoma encephalitis encephalomyelitis epithelial malignant thymoma hepatitis B hepatitis C myelitis obesity ovarian cancer ovarian carcinoma polyp of middle ear thymic carcinoma thymoma thymus squamous cell carcinoma tuberculosis type 2 diabetes mellitus viral infectious disease
4978	opioid binding protein/cell adhesion molecule like	OPCML Aliases: IGLON1 IgLON family member 1 OBCAM OPCM	Homo sapiens (human)	Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma adenocarcinoma adenoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 6 arthritis arthropathy bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder urothelial carcinoma brain cancer breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma cholangiocarcinoma congenital heart disease cribriform carcinoma depressive disorder dermoid cyst of ovary distal arthrogryposis dysgerminoma embryoma esophagus squamous cell carcinoma gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma idiopathic scoliosis intrahepatic cholangiocarcinoma liver cancer liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder melancholic depression mixed glioma nasopharynx carcinoma neurotic disorder nicotine dependence obsolete melancholia obsolete ymphosarcoma osteoarthritis ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma prostate lymphoma sarcomatoid carcinoma schizophrenia steatotic liver disease stomach cancer stomach carcinoma tubular adenocarcinoma urinary bladder cancer
55454	chondroitin sulfate N-acetylgalactosaminyltransferase 2	CSGALNACT2 Aliases: GALNACT-2 GALNACT2 MGC40204 PRO0082 chondroitin beta1,4 N-acetylgalactosaminyltransferase 2 glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase 2	Homo sapiens (human)	Hirschsprung's disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis multiple sclerosis

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