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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 **392176 - 392200** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
29926	GDP-mannose pyrophosphorylase A	GMPPA	Homo sapiens (human)	Addison's disease Down syndrome Laron syndrome achalasia achondroplasia adrenal cortical hypofunction alacrima, achalasia, and impaired intellectual development syndrome blindness coloboma epilepsy intellectual disability learning disability megaesophagus microcephaly nonepidermolytic palmoplantar keratoderma optic atrophy palmoplantar keratosis sensorineural hearing loss triple-A syndrome visual epilepsy
29925	GDP-mannose pyrophosphorylase B	GMPPB Aliases: KIAA1851 mannose-1-phosphate guanyltransferase beta	Homo sapiens (human)	Bell's palsy Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Lambert-Eaton myasthenic syndrome Walker-Warburg syndrome agnosia amblyopia 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 bilateral optic nerve hypoplasia blindness cardiomyopathy cataract centronuclear myopathy cleft palate clubfoot coloboma communicating hydrocephalus cone-rod dystrophy congenital muscular dystrophy-dystroglycanopathy A14 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy cryptorchidism developmental coordination disorder dissociated nystagmus distal myopathy endomyocardial fibrosis epilepsy esotropia facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fundus albipunctatus glaucoma holoprosencephaly 1 holoprosencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia idiopathic generalized epilepsy intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy mechanical strabismus megalocornea meningocele microcephaly microphthalmia monocular esotropia muscular dystrophy-dystroglycanopathy type B14 muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy oligohydramnios ophthalmoplegia optic atrophy pathologic nystagmus ptosis retinal detachment retinitis pigmentosa rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss speech disorder spontaneous ocular nystagmus strabismic amblyopia strabismus syndromic X-linked intellectual disability 94 visual epilepsy
29906	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5	ST8SIA5 Aliases: ST8Sia V	Homo sapiens (human)	idiopathic scoliosis
29880	ALG5 dolichyl-phosphate beta-glucosyltransferase	ALG5 Aliases: bA421P11.2	Homo sapiens (human)	congenital disorder of glycosylation type I polycystic kidney disease
29858	phosphomannomutase 1	Pmm1	Mus musculus (house mouse)	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I
29758	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	St6galnac3	Rattus norvegicus (Norway rat)
29750	polypeptide N-acetylgalactosaminyltransferase 7	Galnt7	Rattus norvegicus (Norway rat)
29640	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	Rattus norvegicus (Norway rat)	congenital disorder of glycosylation Iu
29633	N-deacetylase and N-sulfotransferase 1	Ndst1	Rattus norvegicus (Norway rat)	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
29623	UDP-glucuronosyltransferase 2 family, member 37	Ugt2b37	Rattus norvegicus (Norway rat)
29595	5-hydroxytryptamine receptor 2A	Htr2a	Rattus norvegicus (Norway rat)	Alzheimer's disease alcohol dependence alcohol use disorder alcoholic psychosis anorexia nervosa autism spectrum disorder bladder neck obstruction chronic obstructive pulmonary disease cocaine abuse cocaine dependence congenital diaphragmatic hernia congestive heart failure depressive disorder hyperglycemia hypertension inflammatory and toxic neuropathy major depressive disorder nicotine dependence non-alcoholic fatty liver obesity obsessive-compulsive disorder pancreatitis pathological gambling schizophrenia steatotic liver disease withdrawal disorder
29582	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Mgat3	Rattus norvegicus (Norway rat)
29535	pancreatic and duodenal homeobox 1	Pdx1	Rattus norvegicus (Norway rat)	acute necrotizing pancreatitis cerebral infarction diabetes mellitus diabetic retinopathy hyperglycemia maturity-onset diabetes of the young type 4 maturity-onset diabetes of the young obesity pancreatic agenesis placental insufficiency type 1 diabetes mellitus type 2 diabetes mellitus
29484	solute carrier family 3 member 1	Slc3a1	Rattus norvegicus (Norway rat)	cystinuria
29353	phosphorylase kinase catalytic subunit gamma 1	Phkg1	Rattus norvegicus (Norway rat)
29309	coenzyme Q3 methyltransferase	Coq3	Rattus norvegicus (Norway rat)
29260	toll-like receptor 4	Tlr4	Rattus norvegicus (Norway rat)	Alzheimer's disease Behcet's disease Kawasaki disease acute kidney failure acute necrotizing pancreatitis allergic conjunctivitis allergic contact dermatitis allergic rhinitis ankylosing spondylitis anogenital venereal wart anterior uveitis arteriosclerosis arthritis asthma atopic dermatitis breast cancer carotid artery disease carotid stenosis cholesteatoma of middle ear cholesteatoma chronic obstructive pulmonary disease colitis collagen disease coronary artery disease cutaneous leishmaniasis cystic echinococcosis cystic fibrosis dermatomyositis diabetes mellitus diabetic neuropathy diabetic retinopathy dry eye syndrome end stage renal disease exfoliation syndrome eye disease familial mediterranean fever glucose metabolism disease hepatocellular carcinoma hepatorenal syndrome herpes simplex virus keratitis ileitis invasive aspergillosis keratitis kidney failure liver cirrhosis low tension glaucoma lung disease macular degeneration mastitis mastoiditis melanoma meningococcal meningitis metabolic dysfunction-associated steatotic liver disease multiple sclerosis myocardial infarction obesity otitis media pancreatitis perinatal necrotizing enterocolitis pleural tuberculosis pre-eclampsia primary immunodeficiency disease primary open angle glaucoma psoriasis pulmonary emphysema pulmonary tuberculosis pulpitis renal fibrosis respiratory allergy respiratory syncytial virus infectious disease sciatic neuropathy sinusitis suppurative otitis media temporal arteritis tympanosclerosis type 1 diabetes mellitus type 2 diabetes mellitus urinary tract infection uveitis vitiligo
29095	ORMDL sphingolipid biosynthesis regulator 2	ORMDL2 Aliases: HSPC160 MST095 MSTP095 adoplin-2	Homo sapiens (human)	allergic asthma asthma intrinsic asthma
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
28992	mono-ADP ribosylhydrolase 1	MACROD1 Aliases: LRP16	Homo sapiens (human)	acute monocytic leukemia atypical chronic myeloid leukemia, BCR-ABL1 negative bipolar disorder breast cancer breast carcinoma cancer cardiovascular system disease childhood leukemia chronic monocytic leukemia colorectal cancer colorectal carcinoma disease of metabolism embryoma endometrial cancer endometrial carcinoma gout heart disease hepatocellular carcinoma large intestine cancer leukemia liver cancer lymphoid leukemia monocytic leukemia myeloid leukemia nicotine dependence pancreatic cancer pancreatic carcinoma prolactinoma uterine corpus cancer
28146	stress-associated endoplasmic reticulum protein 1	Serp1	Mus musculus (house mouse)
27430	methionine adenosyltransferase 2 non-catalytic beta subunit	MAT2B	Homo sapiens (human)
27426	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	Nagpa	Mus musculus (house mouse)
27376	solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10	Slc25a10	Mus musculus (house mouse)	mitochondrial DNA depletion syndrome 19 mitochondrial DNA depletion syndrome mitochondrial complex I deficiency myoclonic-atonic epilepsy
27357	glycogenin 1	Gyg1	Mus musculus (house mouse)	glycogen storage disease XV glycogen storage disease

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