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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 **2326 - 2350** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
4048	leukotriene A4 hydrolase	LTA4H	Homo sapiens (human)	Burkitt lymphoma Buruli ulcer disease Crohn's colitis Crohn's disease Down syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute myocardial infarction adenocarcinoma adenoma allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial meningitis cancer cardiovascular system disease cerebral infarction cerebrovascular disease chronic myeloid leukemia colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma depressive disorder dysthymic disorder embryoma familial nephrotic syndrome granular cell carcinoma heart disease human immunodeficiency virus infectious disease idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma large intestine cancer laryngeal squamous cell carcinoma leprosy lipoid nephrosis major depressive disorder melancholic depression melanoma myeloproliferative disorder with eosinophilia myocardial infarction nephrotic syndrome neurotic disorder obsolete melancholia pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma pulmonary tuberculosis silent myocardial infarction skin benign neoplasm skin cancer skin melanoma squamous cell carcinoma squamous cell neoplasm tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma ulcerative colitis viral meningitis
93183	phosphatidylinositol glycan anchor biosynthesis class M	PIGM Aliases: DPM:GlcN-(acyl-)PI mannosyltransferase GPI mannosyltransferase 1 GPI-MT-I PIG-M dol-P-Man dependent GPI mannosyltransferase	Homo sapiens (human)	Budd-Chiari syndrome epilepsy focal epilepsy paroxysmal nocturnal hemoglobinuria partial motor epilepsy portal hypertension portal vein thrombosis thrombophilia visual epilepsy
2822	glycosylphosphatidylinositol specific phospholipase D1	GPLD1	Homo sapiens (human)	Budd-Chiari syndrome Norum disease Richter's syndrome Tangier disease abetalipoproteinemia acute myocardial infarction arteriosclerotic cardiovascular disease atherosclerosis brain infarction breast cancer breast carcinoma cancer carcinoma choreaacanthocytosis chronic lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease coronary thrombosis embryoma hypolipoproteinemia large intestine cancer melanoma myocardial infarction nutmeg liver osteoporosis papillary carcinoma prostate cancer prostate carcinoma rheumatoid arthritis sarcomatoid carcinoma silent myocardial infarction skin melanoma succinic semialdehyde dehydrogenase deficiency thyroid adenoma thyroid cancer thyroid gland carcinoma
333433	glycerol-3-phosphate dehydrogenase 1-like	Gpd1l	Mus musculus (house mouse)	Brugada syndrome 2
176399	Glycerol-3-phosphate dehydrogenase [NAD(+)];putative glycerol-3-phosphate dehydrogenase 2	gpdh-2	Caenorhabditis elegans	Brugada syndrome 2
33824	Glycerol-3-phosphate dehydrogenase 1	Gpdh1	Drosophila melanogaster (fruit fly)	Brugada syndrome 2
851539	glycerol-3-phosphate dehydrogenase (NAD(+)) GPD1	GPD1	Saccharomyces cerevisiae S288C	Brugada syndrome 2
449663	glycerol-3-phosphate dehydrogenase 1 like	gpd1l	Danio rerio (zebrafish)	Brugada syndrome 2
379962	glycerol-3-phosphate dehydrogenase 1 like L homeolog	gpd1l.L	Xenopus laevis (African clawed frog)	Brugada syndrome 2
394623	glycerol-3-phosphate dehydrogenase 1 like	gpd1l	Xenopus tropicalis (tropical clawed frog)	Brugada syndrome 2
854095	glycerol-3-phosphate dehydrogenase (NAD(+)) GPD2	GPD2	Saccharomyces cerevisiae S288C	Brugada syndrome 2
23171	glycerol-3-phosphate dehydrogenase 1 like	GPD1L Aliases: KIAA0089	Homo sapiens (human)	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation congestive heart failure coronary artery disease head and neck squamous cell carcinoma nutmeg liver osteoarthritis sick sinus syndrome steatotic liver disease sudden infant death syndrome
781	calcium voltage-gated channel auxiliary subunit alpha2delta 1	CACNA2D1 Aliases: alpha2delta-1 lncRNA-N3	Homo sapiens (human)	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome West syndrome Williams-Beuren syndrome acute myeloid leukemia amelogenesis imperfecta type 1G atrial fibrillation atrioventricular block azoospermia brain infarction cancer cardiac arrest colon cancer colonic benign neoplasm colorectal cancer depressive disorder developmental and epileptic encephalopathy 110 embryoma epilepsy essential hypertension glaucoma hepatocellular carcinoma hypertension idiopathic scoliosis intellectual disability large intestine cancer learning disability liver cancer major depressive disorder malignant hyperthermia melancholic depression neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia primary open angle glaucoma short QT syndrome sick sinus syndrome stomach cancer stomach carcinoma supravalvular aortic stenosis uveal melanoma
39265	procollagen lysyl hydroxylase	Plod	Drosophila melanogaster (fruit fly)	Bruck syndrome Ehlers-Danlos syndrome kyphoscoliotic type 1 Ehlers-Danlos syndrome hepatocellular carcinoma hypothyroidism lung adenocarcinoma
54995	3-oxoacyl-ACP synthase, mitochondrial	OXSM Aliases: CEM1 FASN2D FLJ20604 KS beta-ketoacyl synthase	Homo sapiens (human)	Brucella melitensis brucellosis breast cancer tuberculosis
6441	surfactant protein D	SFTPD Aliases: COLEC7 SP-D	Homo sapiens (human)	Bloch-Sulzberger syndrome Coronavirus infectious disease Crohn's colitis Crohn's disease Ebola hemorrhagic fever Fabry disease Wolman disease acquired immunodeficiency syndrome acute interstitial pneumonia acute lymphoblastic leukemia acute pancreatitis adenocarcinoma adenoid hypertrophy adenoma adult acute lymphocytic leukemia adult respiratory distress syndrome allergic asthma allergic disease allergic rhinitis anthracosilicosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asthma atherosclerosis bacterial pneumonia bacterial sepsis blastomycosis brain stem infarction breast cancer bronchiectasis bronchiolitis obliterans bronchiolitis bronchitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma byssinosis cancer cardiovascular system disease cataract 32 multiple types cerebral artery occlusion cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia chronic ethmoiditis chronic interstitial cystitis chronic obstructive pulmonary disease chronic sphenoidal sinusitis chylomicron retention disease colitis communicating hydrocephalus cone-rod dystrophy congenital diaphragmatic hernia congestive heart failure corneal ulcer coronary artery disease coronary stenosis craniosynostosis cribriform carcinoma cystic fibrosis diabetes mellitus diabetic ketoacidosis disease of metabolism dry eye syndrome embryoma fundus albipunctatus gastroenteritis glomerulonephritis granular cell carcinoma heart disease herpes simplex virus keratitis human immunodeficiency virus infectious disease hydrocephalus hypereosinophilic syndrome hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease influenza interstitial cystitis interstitial lung disease interstitial nephritis intrinsic asthma kidney disease leprosy leukopenia lipid storage disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis lymphoblastic lymphoma middle cerebral artery infarction mixed connective tissue disease nephritis nephrosis neurogenic arthropathy newborn respiratory distress syndrome nutmeg liver obesity obstructive hydrocephalus obstructive lung disease osteoarthritis ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis paracoccidioidomycosis parapsoriasis periodontitis peripheral artery disease periventricular leukomalacia pneumocystosis pneumonia postinflammatory pulmonary fibrosis pre-malignant neoplasm prostate adenocarcinoma prostate cancer prostate carcinoma prune belly syndrome psoriasis pulmonary alveolar proteinosis pulmonary emphysema pulmonary fibrosis pustulosis of palm and sole pyelitis pyelonephritis pyoureter renal infectious disease respiratory failure respiratory syncytial virus infectious disease retinitis pigmentosa rheumatoid arthritis rhinitis sarcoidosis scleroderma senile degeneration of brain sickle cell anemia silicosis sinusitis squamous cell carcinoma sudden infant death syndrome systemic lupus erythematosus systemic primary carnitine deficiency disease systemic scleroderma tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary tract obstruction vasomotor rhinitis viral infectious disease xerophthalmia
50814	NAD(P) dependent steroid dehydrogenase-like	NSDHL Aliases: H105e3 SDR31E1 XAP104 short chain dehydrogenase/reductase family 31E, member 1	Homo sapiens (human)	Bloch-Sulzberger syndrome CHILD syndrome CK syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia cancer chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy
1291	collagen type VI alpha 1 chain	COL6A1	Homo sapiens (human)	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
12833	collagen, type VI, alpha 1	Col6a1	Mus musculus (house mouse)	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
3964	galectin 8	LGALS8 Aliases: PCTA-1	Homo sapiens (human)	Bernard-Soulier syndrome Glanzmann's thrombasthenia alopecia areata arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer embryoma encephalitis encephalomyelitis enthesopathy fibromyalgia giant cell glioblastoma glioblastoma gray platelet syndrome high grade glioma immune system disease large intestine cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma lymphopenia multiple myeloma multiple sclerosis myasthenia gravis myelitis nodular prostate nonpapillary renal cell carcinoma osteoarthritis osteoporosis ovarian cancer ovarian carcinoma papillary renal cell carcinoma platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 prostate cancer prostate carcinoma prostatic adenoma qualitative platelet defect renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma squamous cell carcinoma systemic lupus erythematosus tongue squamous cell carcinoma viral infectious disease
199857	ALG14 UDP-N-acetylglucosaminyltransferase subunit	ALG14 Aliases: MGC19780	Homo sapiens (human)	Bell's palsy agnosia clubfoot congenital myasthenic syndrome 15 congenital myasthenic syndrome congenital ptosis developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis idiopathic scoliosis intellectual disability isolated elevated serum creatine phosphokinase levels learning disability myopathy ptosis scoliosis syndromic X-linked intellectual disability 94
85365	ALG2 alpha-1,3/1,6-mannosyltransferase	ALG2 Aliases: CDG1I CDGIi FLJ14511 NET38 hALPG2	Homo sapiens (human)	Bell's palsy agnosia blindness breast cancer breast carcinoma cancer cataract clubfoot coloboma congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation congenital myasthenic syndrome 14 congenital myasthenic syndrome congenital nystagmus congenital ptosis developmental coordination disorder dissociated nystagmus embryoma epilepsy facial nerve disease facial paralysis familial periodic paralysis giant cell glioblastoma glioblastoma high grade glioma intellectual disability isolated elevated serum creatine phosphokinase levels learning disability myopathy obsolete infantile epileptic encephalopathy pathologic nystagmus ptosis scoliosis spontaneous ocular nystagmus visual epilepsy
64419	myotubularin related protein 14	MTMR14 Aliases: FLJ22405 FLJ90311 egg-derived tyrosine phosphatase homolog (Drosophila) hEDTP hJumpy	Homo sapiens (human)	Bell's palsy agnosia asphyxia neonatorum autosomal dominant centronuclear myopathy autosomal recessive centronuclear myopathy cancer capillary hemangioma cardiomyopathy cavernous hemangioma centronuclear myopathy 1 centronuclear myopathy X-linked centronuclear myopathy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital myopathy 4A congenital ptosis congenital structural myopathy cryptorchidism developmental coordination disorder endomyocardial fibrosis facial nerve disease facial paralysis familial periodic paralysis hemangioma hepatocellular carcinoma hypertrophic cardiomyopathy liver cancer liver carcinoma malignant hyperthermia megaconial type congenital muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy obesity ophthalmoplegia ovarian carcinoma polyhydramnios ptosis rigid spine muscular dystrophy 1 tubular aggregate myopathy 1
79868	ALG13 UDP-N-acetylglucosaminyltransferase subunit	ALG13 Aliases: CDG1S FLJ23018 MDS031 N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase TDRD13 YGL047W tudor domain containing 13	Homo sapiens (human)	Bell's palsy Meckel's diverticulum West syndrome agnosia attention deficit hyperactivity disorder autistic disorder blindness cerebral degeneration choreatic disease clubfoot congenital disorder of glycosylation type I congenital disorder of glycosylation congenital nystagmus craniosynostosis developmental and epileptic encephalopathy 36 dissociated nystagmus epilepsy facial nerve disease facial paralysis focal segmental glomerulosclerosis hypophosphatemia intellectual disability learning disability lung cancer lung non-small cell carcinoma microcephaly non-syndromic X-linked intellectual disability obesity obsolete infantile epileptic encephalopathy optic atrophy pathologic nystagmus placental insufficiency pyloric stenosis spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
2673	glutamine--fructose-6-phosphate transaminase 1	GFPT1 Aliases: GFA GFAT GFAT1	Homo sapiens (human)	Bell's palsy Laron syndrome Machado-Joseph disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Zollinger-Ellison syndrome achondroplasia agnosia brain cancer breast cancer breast carcinoma cancer centronuclear myopathy clubfoot congenital myasthenic syndrome 12 congenital myasthenic syndrome 4C congenital myasthenic syndrome congenital ptosis congenital structural myopathy developmental coordination disorder diabetes mellitus diabetic ketoacidosis embryoma facial nerve disease facial paralysis familial hyperlipidemia familial periodic paralysis giant cell glioblastoma glioblastoma glomerulonephritis hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertropia isolated elevated serum creatine phosphokinase levels kidney disease liver cancer mechanical strabismus myopathy nasopharynx carcinoma nephritis nephrosis neuromuscular disease neuromuscular junction disease obesity ophthalmoplegia pancreatic cancer pancreatic carcinoma ptosis pyoureter scoliosis stomach cancer stomach carcinoma strabismus tubular aggregate myopathy 1 type 2 diabetes mellitus

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