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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 **391876 - 391900** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
51046	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3	ST8SIA3 Aliases: ST8Sia III	Homo sapiens (human)	acute myeloid leukemia basal ganglia disease cancer embryoma schizophrenia
51006	solute carrier family 35 member C2	SLC35C2 Aliases: CGI-15 bA394O2.1	Homo sapiens (human)
51005	amidohydrolase domain containing 2	AMDHD2 Aliases: CGI-14 N-acetylglucosamine-6-phosphate deacetylase	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
51000	solute carrier family 35 member B3	SLC35B3 Aliases: 3' phosphoadenosine 5' phosphosulfate transporter 2 CGI-19 PAPST2 dJ453H5.1	Homo sapiens (human)	diabetes mellitus type 2 diabetes mellitus
50999	transmembrane p24 trafficking protein 5	TMED5 Aliases: CGI-100 p24g2 p24gamma2	Homo sapiens (human)	T-cell acute lymphoblastic leukemia West Nile fever acute myocardial infarction adult T-cell leukemia/lymphoma breast cancer cancer central nervous system cancer chronic fatigue syndrome coronary thrombosis embryoma encephalitis encephalomyelitis exudative vitreoretinopathy 1 exudative vitreoretinopathy gliosarcoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma liver cancer melanoma mixed glioma multiple sclerosis myelitis myocardial infarction retinopathy of prematurity schizophrenia silent myocardial infarction skin melanoma
50935	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6	St6galnac6	Mus musculus (house mouse)
50877	neuraminidase 3	Neu3	Mus musculus (house mouse)
50863	neurotrimin	NTM Aliases: CEPU-1 HNT IGLON2 IgLON family member 2 NTRI neurotrimin	Homo sapiens (human)	Kartagener syndrome Mycobacterium avium complex disease Parkinson's disease acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bronchiectasis cancer chronic obstructive pulmonary disease congenital aphakia congenital heart disease congestive heart failure coronary thrombosis depressive disorder embryoma endophthalmitis esophagitis familial medullary thyroid carcinoma gallbladder disease gastroesophageal reflux disease hepatocellular carcinoma intracranial aneurysm late onset Parkinson's disease leprosy liver cancer liver disease lung disease lymphadenitis major depressive disorder melancholic depression multiple endocrine neoplasia type 2A myocardial infarction myopia neurotic disorder nicotine dependence obsolete melancholia peptic esophagitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary open angle glaucoma pulmonary tuberculosis schizophrenia seborrheic keratosis silent myocardial infarction skin disease thyroid gland medullary carcinoma tuberculosis tuberculous pneumothorax
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
50799	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	Slc25a13	Mus musculus (house mouse)	adult-onset type II citrullinemia citrullinemia common bile duct disease intrahepatic cholestasis neonatal-onset type II citrullinemia
50798	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	Gne	Mus musculus (house mouse)	GNE myopathy sialuria
50787	heparan sulfate 6-O-sulfotransferase 3	Hs6st3	Mus musculus (house mouse)
50786	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Mus musculus (house mouse)	Paganini-Miozzo syndrome
50785	heparan sulfate 6-O-sulfotransferase 1	Hs6st1	Mus musculus (house mouse)	hypogonadotropic hypogonadism 15 with or without anosmia
50721	sirtuin 6	Sirt6	Mus musculus (house mouse)	metabolic dysfunction-associated steatotic liver disease obesity progeria transient cerebral ischemia
50686	glycogen synthase kinase 3 alpha	Gsk3a	Rattus norvegicus (Norway rat)	Parkinsonism amyotrophic lateral sclerosis
50622	solute carrier family 23 member 2	Slc23a2	Rattus norvegicus (Norway rat)
50614	polypeptide N-acetylgalactosaminyltransferase 9	GALNT9 Aliases: GALNAC-T9 polypeptide GalNAc transferase 9	Homo sapiens (human)	breast cancer breast carcinoma cancer neuroblastoma
50567	solute carrier family 3 member 2	Slc3a2	Rattus norvegicus (Norway rat)	adenoid cystic carcinoma lung adenocarcinoma lung non-small cell carcinoma lung pleomorphic carcinoma stomach carcinoma tongue squamous cell carcinoma transitional cell carcinoma
50555	UDP glycosyltransferase 8	Ugt8	Rattus norvegicus (Norway rat)
50515	carbohydrate sulfotransferase 11	CHST11 Aliases: C4ST C4ST1 C4St-1 HSA269537 chondroitin 4-sulfotransferase 1	Homo sapiens (human)	Barrett's esophagus Costello syndrome Richter's syndrome arthritis arthropathy breast cancer breast carcinoma cancer chronic lymphocytic leukemia hepatocellular carcinoma leukoencephalopathy with vanishing white matter liver cancer osteoarthritis ovarian cancer ovarian carcinoma schizophrenia scoliosis
50487	phospholipase A2 group III	PLA2G3 Aliases: GIII-SPLA2	Homo sapiens (human)	acute myocardial infarction cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary thrombosis embryoma large intestine cancer myocardial infarction silent myocardial infarction
48775	Polypeptide N-acetylgalactosaminyltransferase 35A	Pgant35A	Drosophila melanogaster (fruit fly)
48224	Adenine phosphoribosyltransferase	Aprt	Drosophila melanogaster (fruit fly)	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
47764	Amylase proximal	Amy-p	Drosophila melanogaster (fruit fly)

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