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	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 **1176 - 1200** of **1582** in total

« First

‹ Prev

…

44

45

46

47

48

49

50

51

52

…

Next ›

Last »
Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
64180	dipeptidase 3	DPEP3	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis coronary artery disease laryngeal disease tracheal disease
64377	carbohydrate sulfotransferase 8	CHST8 Aliases: GALNAC4ST-1	Homo sapiens (human)	allergic asthma asthma atopic dermatitis colorectal cancer colorectal carcinoma intrinsic asthma large intestine cancer parapsoriasis peeling skin syndrome psoriasis pustulosis of palm and sole scleroderma skin disease systemic scleroderma
64386	matrix metallopeptidase 25	MMP25 Aliases: MT6-MMP	Homo sapiens (human)	X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 acoustic neuroma acute pericementitis adult fibrosarcoma aggressive periodontitis amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta anaplastic astrocytoma angiomatous meningioma arthritis arthropathy benign meningioma brain cancer breast cancer breast carcinoma cancer carcinoma cerebral convexity meningioma childhood cerebral astrocytoma clear cell meningioma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dental fluorosis dentin dysplasia dentinogenesis imperfecta embryoma fibrillary astrocytoma fibrosarcoma fibrous meningioma gemistocytic astrocytoma giant cell glioblastoma glioblastoma in situ carcinoma intraorbital meningioma intraventricular meningioma juvenile pilocytic astrocytoma large intestine cancer laryngeal squamous cell carcinoma malignant astrocytoma melanoma meningioma meningothelial meningioma microcystic meningioma multiple myeloma multiple sclerosis olfactory groove meningioma osteoarthritis parasagittal meningioma periodontosis pilocytic astrocytoma pituitary adenoma protoplasmic astrocytoma psammomatous meningioma rheumatoid arthritis sarcomatoid carcinoma secretory meningioma skin melanoma spinal meningioma stomach cancer stomach carcinoma subependymal giant cell astrocytoma transitional meningioma
64409	polypeptide N-acetylgalactosaminyltransferase 17	GALNT17 Aliases: GALNTL3 GalNAc-T17 GalNAc-T19 GalNAc-T5L polypeptide GalNAc transferase 3 polypeptide N-acetylgalactosaminyltransferase-like 3 ppGalNAc-T17	Homo sapiens (human)	allergic asthma asthma autism spectrum disorder autistic disorder intrinsic asthma
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
64579	N-deacetylase and N-sulfotransferase 4	NDST4	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder azoospermia cancer colorectal cancer colorectal carcinoma coronary artery disease embryoma intellectual disability large intestine cancer nutmeg liver prostate cancer prostate carcinoma
64581	C-type lectin domain containing 7A	CLEC7A Aliases: CD369 DECTIN-1 SCARE2 hDectin-1	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 Behcet's disease Bloch-Sulzberger syndrome Kawasaki disease Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Pick's disease Reye syndrome acquired hyperkeratosis acute myeloid leukemia adult-onset Still's disease allergic asthma amyloidosis angular cheilitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aspergillosis asthma atherosclerosis atopic dermatitis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome bacterial infectious disease bacterial sepsis black piedra blastomycosis cancer candidiasis cerebral degeneration cheilitis cholesteatoma chromoblastomycosis chronic mucocutaneous candidiasis chronic obstructive pulmonary disease chronic ulcer of skin coccidioidomycosis colitis congenital intrinsic factor deficiency coronary artery disease cryptococcosis cutaneous leishmaniasis cystic fibrosis dermatitis dermatomycosis dermatophytosis diverticulitis embryoma epilepsy exanthem fungal infectious disease gastroenteritis granuloma annulare hepatitis B hepatitis hepatocellular carcinoma histoplasmosis hypomelanosis of Ito ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intrinsic asthma keratitis keratoconjunctivitis lip disease liver cancer liver carcinoma liver cirrhosis lupus nephritis male infertility mycotic corneal ulcer nutmeg liver obesity oral candidiasis osteoarthritis pancreatic cancer pancreatic carcinoma paracoccidioidomycosis parapsoriasis parasitic helminthiasis infectious disease patent ductus arteriosus pneumocystosis pneumonia polyp of middle ear psoriasis pustulosis of palm and sole rheumatoid arthritis shigellosis sporotrichosis superficial mycosis systemic lupus erythematosus tinea favosa tuberculosis ulcerative colitis urinary tract obstruction vasculitis visual epilepsy vulvovaginal candidiasis white piedra
64600	phospholipase A2 group IIF	PLA2G2F	Homo sapiens (human)
64711	heparan sulfate-glucosamine 3-sulfotransferase 6	HS3ST6	Homo sapiens (human)	anthracosilicosis asbestosis bagassosis hereditary angioedema herpes simplex pneumoconiosis siderosis
64761	poly(ADP-ribose) polymerase family member 12	PARP12 Aliases: ARTD12 FLJ22693 PARP-12 ZC3H1	Homo sapiens (human)	Zika fever age related macular degeneration cancer coronary artery disease degeneration of macula and posterior pole hepatocellular carcinoma influenza liver cancer macular degeneration viral infectious disease vitiligo
64768	inositol-pentakisphosphate 2-kinase	IPPK Aliases: FLJ13163 INSP5K2 IP5K IPK1	Homo sapiens (human)	diabetic ketoacidosis obsolete type 1 diabetes mellitus 9 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
64772	endo-beta-N-acetylglucosaminidase	ENGASE Aliases: Di-N-acetylchitobiosyl beta-N-acetylglucosaminidase FLJ21865 Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase	Homo sapiens (human)	NGLY1-deficiency breast cancer breast carcinoma rheumatoid arthritis
64781	ceramide kinase	CERK Aliases: DKFZp434E0211 FLJ21430 FLJ23239 KIAA1646 LK4 dA59H18.2 dA59H18.3 hCERK	Homo sapiens (human)	Kaposi's sarcoma breast cancer breast carcinoma cancer colitis gastroenteritis ileitis ileocolitis microphthalmia neuroblastoma obesity obsolete Matthew-Wood syndrome schizophrenia 10 schizophrenia
64834	ELOVL fatty acid elongase 1	ELOVL1 Aliases: Ssc1	Homo sapiens (human)	Cauda equina syndrome acanthosis nigricans acrodermatitis adrenoleukodystrophy cancer dermatitis dry eye syndrome hyperglycemia neurogenic bladder obsolete asthenopia xerophthalmia
64841	glucosamine-phosphate N-acetyltransferase 1	GNPNAT1 Aliases: FLJ10607 Gpnat1	Homo sapiens (human)	cancer diabetes mellitus diabetic ketoacidosis keratosis follicularis spinulosa decalvans type 2 diabetes mellitus
64847	spermatogenesis associated 20	SPATA20	Homo sapiens (human)	oligoasthenoteratozoospermia
64850	ethanolamine-phosphate phospho-lyase	ETNPPL	Homo sapiens (human)	bipolar disorder borderline personality disorder cancer hepatocellular carcinoma intermittent explosive disorder liver cancer schizophrenia steatotic liver disease
64900	lipin 3	LPIN3 Aliases: SMP2	Homo sapiens (human)	lipid metabolism disorder lung cancer lung non-small cell carcinoma myoglobinuria obesity
64921	CAS1 domain containing 1	CASD1	Homo sapiens (human)
65078	reticulon 4 receptor	RTN4R Aliases: NOGO receptor NOGOR	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 Balo concentric sclerosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome X-linked ichthyosis acute myeloid leukemia adrenoleukodystrophy adult lymphoma amyotrophic lateral sclerosis type 1 anaplastic astrocytoma autism spectrum disorder autistic disorder brain cancer brain disease brain stem infarction cancer central nervous system cancer central nervous system disease central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood leukemia childhood lymphoma chronic fatigue syndrome ciliary body disease colorectal cancer colorectal carcinoma diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy embryoma encephalitis encephalomyelitis essential tremor fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance hepatocellular carcinoma high grade glioma iris disease juvenile pilocytic astrocytoma large intestine cancer leukemia liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma lung small cell carcinoma lymphoma malignant astrocytoma malignant pleural mesothelioma melanoma mixed glioma multiple sclerosis myelitis narcolepsy nasopharynx carcinoma nervous system disease neuroblastoma obsolete ymphosarcoma optic neuritis panuveitis pilocytic astrocytoma prediabetes syndrome protoplasmic astrocytoma psychotic disorder relapsing-remitting multiple sclerosis schizoaffective disorder schizophrenia schizophreniform disorder skin melanoma squamous cell carcinoma subependymal giant cell astrocytoma teratocarcinoma tongue squamous cell carcinoma uveitis
65258	metallophosphoesterase 1	MPPE1 Aliases: Cdc1 PGAP5 post-GPI attachment to proteins 5	Homo sapiens (human)	bipolar disorder borderline personality disorder cancer cerebral malaria chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis B hepatitis influenza intermittent explosive disorder malaria melanoma papillary renal cell carcinoma pneumonia renal cell carcinoma sarcomatoid renal cell carcinoma skin melanoma
65985	acetoacetyl-CoA synthetase	AACS Aliases: ACSF1 FLJ12389 SUR-5 acyl-CoA synthetase family member 1	Homo sapiens (human)	acute myeloid leukemia bacterial sepsis idiopathic scoliosis neuroblastoma obesity steatotic liver disease
66004	Ly6/neurotoxin 1	LYNX1 Aliases: SLURP2	Homo sapiens (human)	allergic asthma asthma breast adenocarcinoma bronchus cancer bronchus carcinoma colon carcinoma colorectal cancer intrinsic asthma lung cancer lung carcinoma parapsoriasis psoriasis pustulosis of palm and sole
66005	chitinase domain containing 1	CHID1 Aliases: FLJ42707 MGC3234 SI-CLP stabilin-1 interacting chitinase-like protein	Homo sapiens (human)	bronchitis rheumatoid arthritis
78989	collectin subfamily member 11	COLEC11 Aliases: CL-11 CL-K1 Collectin K1 MGC3279	Homo sapiens (human)	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC syndrome Bloch-Sulzberger syndrome Chagas disease Klippel-Feil syndrome acquired immunodeficiency syndrome bacterial infectious disease bacterial sepsis blepharophimosis cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism disseminated intravascular coagulation enterobiasis glomerulonephritis human immunodeficiency virus infectious disease humeroradial synostosis hypertropia hypomelanosis of Ito intellectual disability intestinal schistosomiasis isolated cleft palate kidney disease learning disability mechanical strabismus nephritis nephrosis neurodegenerative disease omphalocele ophthalmoplegia pneumonia ptosis purpura fulminans pyoureter radioulnar synostosis schistosomiasis scoliosis sensorineural hearing loss spina bifida occulta spondylolisthesis strabismus trichinosis trypanosomiasis tuberculosis umbilical hernia urinary schistosomiasis viral infectious disease

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

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements