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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 **226 - 250** of **1582** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
122970	acyl-CoA thioesterase 4	ACOT4 Aliases: FLJ31235 PTE-Ib PTE2B	Homo sapiens (human)	cerebral infarction cerebrovascular disease
122618	phospholipase D family member 4	PLD4	Homo sapiens (human)	Usher syndrome type 2 Usher syndrome type 3 Usher syndrome colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatitis large intestine cancer retinitis pigmentosa-deafness syndrome rheumatoid arthritis scleroderma systemic lupus erythematosus systemic scleroderma
120227	cytochrome P450 family 2 subfamily R member 1	CYP2R1 Aliases: Vitamin D 25-hydroxylase	Homo sapiens (human)	Ehlers-Danlos syndrome Graves' disease Laron syndrome Sertoli cell-only syndrome Vogt-Koyanagi-Harada disease X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 achondroplasia acute myocardial infarction adenocarcinoma adenoma age related macular degeneration agnosia allergic asthma androgen insensitivity syndrome arteriosclerotic cardiovascular disease asthma atherosclerosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome basal cell carcinoma brain disease brain infarction calcinosis calcium metabolism disease cancer cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole dental enamel hypoplasia dermatitis developmental coordination disorder diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma embryoma endometriosis of uterus endometriosis endometritis essential hypertension eunuchism gestational diabetes goiter granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatitis C hepatocellular carcinoma hypercalcemia hypertension hyperthyroidism hypogonadism hypoparathyroidism hypophosphatemia immune system disease intrinsic asthma large intestine cancer liver cancer liver cirrhosis lung cancer lung non-small cell carcinoma macular degeneration mastitis melanoma mitral valve stenosis multiple sclerosis myocardial infarction nephrocalcinosis nonpapillary renal cell carcinoma nutmeg liver obesity obsolete type 1 diabetes mellitus 9 oligospermia osteogenesis imperfecta osteomalacia pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma phosphorus metabolism disease polycystic ovary syndrome pre-eclampsia premature menopause prostate cancer prostate carcinoma pseudohypoparathyroidism renal carcinoma renal cell carcinoma rheumatoid arthritis rickets sarcomatoid renal cell carcinoma secondary hyperparathyroidism silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease thyroid gland disease thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma tuberculosis 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 type 2 diabetes mellitus vitamin D-dependent rickets type 1B
120071	LARGE xylosyl- and glucuronyltransferase 2	LARGE2 Aliases: FLJ35207 PP5656	Homo sapiens (human)	Duchenne muscular dystrophy acute myocardial infarction autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 cancer congenital muscular dystrophy coronary thrombosis distal myopathy embryoma facioscapulohumeral muscular dystrophy limb-girdle muscular dystrophy muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 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 prostate cancer prostate carcinoma rippling muscle disease 2 silent myocardial infarction transitional cell carcinoma
119548	pancreatic lipase related protein 3	PNLIPRP3	Homo sapiens (human)	hepatocellular carcinoma liver cancer
119391	glutathione S-transferase omega 2	GSTO2	Homo sapiens (human)	Alzheimer's disease Parkinson's disease alcohol use disorder asthma
119180	lysozyme like 2	LYZL2	Homo sapiens (human)	dental caries dentin caries
117248	polypeptide N-acetylgalactosaminyltransferase 15	GALNT15 Aliases: GALNT7 polypeptide GalNAc transferase 15 pp-GalNAc-T15	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
117145	thioesterase superfamily member 4	THEM4 Aliases: C-terminal modulator protein CTMP	Homo sapiens (human)	amyotrophic lateral sclerosis attention deficit hyperactivity disorder breast cancer bronchus cancer bronchus carcinoma cancer central nervous system cancer diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma liver cancer lung benign neoplasm lung cancer lung carcinoma mixed glioma pancreatic adenocarcinoma progressive muscular atrophy type 2 diabetes mellitus
116969	ADP-ribosyltransferase 5	ART5 Aliases: ARTC5	Homo sapiens (human)	cholera
116285	acyl-CoA synthetase medium chain family member 1	ACSM1 Aliases: MACS1	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 carcinoma cerebral palsy depressive disorder essential hypertension hemiplegia hypertension idiopathic scoliosis lung benign neoplasm lung carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia sarcomatoid carcinoma schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
116255	monoacylglycerol O-acyltransferase 1	MOGAT1 Aliases: DGAT2L MGAT1	Homo sapiens (human)	multiple sclerosis overnutrition steatotic liver disease
115290	F-box protein 17	FBXO17 Aliases: F-box only protein 26 FBG4 FLJ11798 FLJ25205 Fbx17 MGC9379	Homo sapiens (human)	cancer embryoma gliosarcoma hepatocellular carcinoma high grade glioma liver cancer lung cancer lung non-small cell carcinoma mixed glioma
115209	OMA1 zinc metallopeptidase	OMA1	Homo sapiens (human)
114805	polypeptide N-acetylgalactosaminyltransferase 13	GALNT13 Aliases: GalNAc-T13 KIAA1918 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 13 polypeptide GalNAc transferase 13	Homo sapiens (human)	cancer chronic obstructive pulmonary disease lung benign neoplasm lung carcinoma sickle cell anemia
114780	polycystin 1 like 2 (gene/pseudogene)	PKD1L2 Aliases: KIAA1879	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease
114132	sialic acid binding Ig like lectin 11	SIGLEC11	Homo sapiens (human)
113829	solute carrier family 35 member A4	SLC35A4	Homo sapiens (human)	breast cancer cancer hepatocellular carcinoma liver cancer lung adenocarcinoma lung cancer multiple myeloma
113622	ADP-ribosylhydrolase like 1	ADPRHL1	Homo sapiens (human)
113612	cytochrome P450 family 2 subfamily U member 1	CYP2U1 Aliases: SPG49 spastic paraplegia 49	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 GM1 gangliosidosis type 1 GM1 gangliosidosis Henoch-Schoenlein purpura MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome agnosia blindness breast cancer breast carcinoma cancer developmental coordination disorder dystonia embryoma focal hand dystonia generalized dystonia hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hypersensitivity vasculitis intellectual disability learning disability neurodegenerative disease neuropathy paraplegia peripheral nervous system disease polyneuropathy syringomyelia
113189	carbohydrate sulfotransferase 14	CHST14 Aliases: D4ST-1 HD4ST	Homo sapiens (human)	Ehlers-Danlos syndrome musculocontractural type 1 Ehlers-Danlos syndrome Marfan syndrome Peters anomaly agnosia 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 brittle cornea syndrome 1 cleft palate clubfoot congenital diaphragmatic hernia cornea plana craniosynostosis cryptorchidism developmental coordination disorder distal arthrogryposis familial nephrotic syndrome familial periodic paralysis glaucoma hiatus hernia hydrocephalus hydronephrosis hypertropia isolated cleft palate lipoid nephrosis mechanical strabismus myopathy myopia nephrotic syndrome obsolete constipation omphalocele ophthalmoplegia osteogenesis imperfecta patent foramen ovale pneumothorax prostate cancer prostate carcinoma retinal detachment scoliosis sensorineural hearing loss situs inversus strabismus tuberous sclerosis umbilical hernia
113026	phospholipase C delta 3	PLCD3	Homo sapiens (human)	Goldenhar syndrome acquired immunodeficiency syndrome alcohol dependence alcohol use disorder arteriosclerotic cardiovascular disease atherosclerosis coronary artery disease human immunodeficiency virus infectious disease microphthalmia nasopharynx carcinoma obsolete Matthew-Wood syndrome senile cataract
112937	galactosidase beta 1 like 3	GLB1L3 Aliases: FLJ90231	Homo sapiens (human)
112817	4-hydroxy-2-oxoglutarate aldolase 1	HOGA1 Aliases: DHDPS2 FLJ37472 N-acetylneuraminate pyruvate lyase 2 (putative) NPL2 dihydrodipicolinate synthetase homolog 2 (E. coli)	Homo sapiens (human)	calcinosis calcium metabolism disease cholestasis chronic kidney disease hypercalcemia nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria type 3 primary hyperoxaluria
94101	ORMDL sphingolipid biosynthesis regulator 1	ORMDL1	Homo sapiens (human)	allergic asthma asthma intrinsic asthma

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