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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	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 **395626 - 395650** of **422592** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
104410375	structural maintenance of chromosomes 3	SMC3	Nestor notabilis (Kea)
104494061	structural maintenance of chromosomes 3	SMC3	Buceros rhinoceros silvestris
104317764	structural maintenance of chromosomes 3	SMC3	Haliaeetus albicilla (white-tailed eagle)
115348162	structural maintenance of chromosomes 3	SMC3	Aquila chrysaetos chrysaetos
112993655	structural maintenance of chromosomes 3	SMC3	Dromaius novaehollandiae (emu)
101019671	structural maintenance of chromosomes 3	SMC3	Papio anubis (olive baboon)
120368886	structural maintenance of chromosomes 3	SMC3	Mauremys reevesii (Reeves's turtle)
129331975	structural maintenance of chromosomes 3	SMC3	Eublepharis macularius
110589622	structural maintenance of chromosomes 3	SMC3	Neomonachus schauinslandi (Hawaiian monk seal)
450731	structural maintenance of chromosomes 3	SMC3	Pan troglodytes (chimpanzee)
103288557	structural maintenance of chromosomes 3	SMC3	Eptesicus fuscus (big brown bat)
128077717	structural maintenance of chromosomes 3	SMC3	Tympanuchus pallidicinctus (lesser prairie-chicken)
102449161	structural maintenance of chromosomes 3	SMC3	Pelodiscus sinensis (Chinese soft-shelled turtle)
118093519	structural maintenance of chromosomes 3	SMC3	Zootoca vivipara (common lizard)
107511388	structural maintenance of chromosomes 3	SMC3	Rousettus aegyptiacus (Egyptian rousette)
107121823	structural maintenance of chromosomes 3	SMC3	Gekko japonicus
115608326	structural maintenance of chromosomes 3	SMC3	Strigops habroptila (Kakapo)
117880171	structural maintenance of chromosomes 3	SMC3	Trachemys scripta elegans
102968584	structural maintenance of chromosomes 3	SMC3	Panthera tigris (tiger)
101138008	structural maintenance of chromosomes 3	SMC3	Gorilla gorilla gorilla (western lowland gorilla)
130579046	structural maintenance of chromosomes 3	SMC3	Malurus melanocephalus (red-backed fairy wren)
106984754	structural maintenance of chromosomes 3	SMC3	Acinonyx jubatus (cheetah)
114058407	structural maintenance of chromosomes 3	SMC3	Empidonax traillii (willow flycatcher)
104347517	structural maintenance of chromosomes 3	SMC3	Leptosomus discolor (cuckoo roller)
9126	structural maintenance of chromosomes 3	SMC3 Aliases: BAM HCAP SMC3L1 bamacan bamacan proteoglycan	Homo sapiens (human)	Burkitt lymphoma Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome 2 Cornelia de Lange syndrome 3 Cornelia de Lange syndrome Dubowitz syndrome Laron syndrome Marfan syndrome Meckel syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Peters anomaly Prader-Willi syndrome Roberts syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Turner syndrome X-linked Aarskog syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adult lymphoma allergic asthma anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis 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 attention deficit hyperactivity disorder atypical chronic myeloid leukemia, BCR-ABL1 negative autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome blepharitis blind hypotensive eye bone cancer bone osteosarcoma bronchus cancer bronchus carcinoma cancer carcinoma cataract 32 multiple types cataract central nervous system lymphoma childhood lymphoma choanal atresia chondrodysplasia-pseudohermaphroditism syndrome chronic interstitial cystitis chronic monocytic leukemia cleft palate cleidocranial dysplasia clubfoot colon carcinoma colorectal cancer cone-rod dystrophy congenital diaphragmatic hernia congenital nystagmus congenital ptosis cornea plana coronary artery disease craniosynostosis cribriform carcinoma cryptorchidism dissociated nystagmus embryoma epilepsy esophagitis fundus albipunctatus gastroesophageal reflux disease generalized anxiety disorder gingivitis glaucoma gonadal dysgenesis granular cell carcinoma hepatocellular carcinoma humeroradial synostosis hydrocephalus hypertrichosis hypertropia hypospadias inguinal hernia intellectual disability interstitial cystitis intestinal benign neoplasm intestinal cancer intestinal volvulus intrinsic asthma isolated cleft palate kidney failure kwashiorkor large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoid leukemia lymphoma marasmus mechanical strabismus megacolon microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly myeloid leukemia myopia neuropathy nutrition disease obsolete SC phocomelia syndrome obsolete ymphosarcoma ophthalmoplegia osteosarcoma patent foramen ovale pathologic nystagmus peptic esophagitis periodontitis peripheral nervous system disease placental insufficiency pneumonia prostate cancer prostate carcinoma protein-energy malnutrition prune belly syndrome ptosis pulmonary valve stenosis pyloric stenosis radioulnar synostosis retinitis pigmentosa sarcomatoid carcinoma sensorineural hearing loss situs inversus speech disorder spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 thromboangiitis obliterans toxic megacolon trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis tubular adenocarcinoma ventricular septal defect vesicoureteral reflux visual epilepsy

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