GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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	October 29, 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 **9651 - 9675** of **9988** in total

« First

‹ Prev

…

383

384

385

386

387

388

389

390

391

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
9184	BUB3 mitotic checkpoint protein	BUB3	Homo sapiens (human)
26035	glucuronic acid epimerase	GLCE Aliases: HSEPI KIAA0836 heparan sulfate epimerase	Homo sapiens (human)	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions amyotrophic lateral sclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebrovascular disease embryoma essential hypertension frontotemporal dementia hypertension luminal breast carcinoma A lung benign neoplasm lung cancer lung carcinoma lung small cell carcinoma nodular prostate progressive muscular atrophy prostate cancer prostate carcinoma prostate disease prostatic adenoma
50632	calcyon neuron specific vesicular protein	CALY	Homo sapiens (human)
92293	transmembrane protein 132C	TMEM132C	Homo sapiens (human)
9038	trace amine associated receptor 5	TAAR5	Homo sapiens (human)
1869	E2F transcription factor 1	E2F1	Homo sapiens (human)
9947	MAGE family member C1	MAGEC1	Homo sapiens (human)
51200	carboxypeptidase A4	CPA4	Homo sapiens (human)
28982	FLVCR choline and heme transporter 1	FLVCR1	Homo sapiens (human)
390442	olfactory receptor family 11 subfamily H member 4	OR11H4	Homo sapiens (human)
23288	IQ motif containing E	IQCE	Homo sapiens (human)
10898	cleavage and polyadenylation specific factor 4	CPSF4	Homo sapiens (human)
5168	ectonucleotide pyrophosphatase/phosphodiesterase 2	ENPP2 Aliases: ATX PD-IALPHA autotaxin	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 Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Pick's disease Reye syndrome actinic keratosis adult hepatocellular carcinoma alternating hemiplegia of childhood arthritis arthropathy ataxia telangiectasia autonomic neuropathy autosomal dominant cerebellar ataxia biliary atresia bladder carcinoma blood coagulation disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood hepatocellular carcinoma choroid plexus cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma dedifferentiated liposarcoma disease of metabolism embryoma epithelioid sarcoma fibrodysplasia ossificans progressiva fibromyalgia gallbladder disease gastroenteritis giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperthyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis liposarcoma liver cancer liver cirrhosis liver disease localized scleroderma lung benign neoplasm lung cancer lung carcinoma multiple myeloma multiple sclerosis myositis ossificans nervous system disease neuroblastoma nodular prostate nonpapillary renal cell carcinoma obesity obsolete inherited blood coagulation disease ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary renal cell carcinoma pleomorphic liposarcoma proliferative diabetic retinopathy prostate cancer prostate carcinoma prostatic adenoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcoma sarcomatoid renal cell carcinoma scleroderma seborrheic keratosis skin disease spindle cell sarcoma spinocerebellar ataxia type 7 systemic scleroderma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis ulcerative colitis urinary bladder cancer
10051	structural maintenance of chromosomes 4	SMC4	Homo sapiens (human)
81502	histocompatibility minor 13	HM13	Homo sapiens (human)
3600	interleukin 15	IL15	Homo sapiens (human)
57453	DS cell adhesion molecule like 1	DSCAML1	Homo sapiens (human)
29954	protein O-mannosyltransferase 2	POMT2 Aliases: Dolichyl-phosphate-mannose--protein mannosyltransferase LGMD2N	Homo sapiens (human)	Axenfeld-Rieger syndrome Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome X-linked dilated cardiomyopathy agnosia 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 buphthalmos campomelic dysplasia cancer cataract cleft lip cleft palate coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A2 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cryptorchidism cystic kidney disease developmental coordination disorder dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy embryoma epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fundus albipunctatus glaucoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hyperopia hypertropia imperforate anus intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly mechanical strabismus megalocornea meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B2 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 ophthalmoplegia optic atrophy peripheral retinal degeneration pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type tuberous sclerosis visual epilepsy
4804	nerve growth factor receptor	NGFR	Homo sapiens (human)
5686	proteasome 20S subunit alpha 5	PSMA5	Homo sapiens (human)
8425	latent transforming growth factor beta binding protein 4	LTBP4	Homo sapiens (human)
4779	NFE2 like bZIP transcription factor 1	NFE2L1	Homo sapiens (human)
84622	zinc finger protein 594	ZNF594	Homo sapiens (human)
7291	twist family bHLH transcription factor 1	TWIST1	Homo sapiens (human)
199675	mast cell expressed membrane protein 1	MCEMP1	Homo sapiens (human)

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements