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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 **1626 - 1650** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
50721	sirtuin 6	Sirt6	Mus musculus (house mouse)	metabolic dysfunction-associated steatotic liver disease obesity progeria transient cerebral ischemia
50785	heparan sulfate 6-O-sulfotransferase 1	Hs6st1	Mus musculus (house mouse)	hypogonadotropic hypogonadism 15 with or without anosmia
50786	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Mus musculus (house mouse)	Paganini-Miozzo syndrome
50787	heparan sulfate 6-O-sulfotransferase 3	Hs6st3	Mus musculus (house mouse)
50798	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	Gne	Mus musculus (house mouse)	GNE myopathy sialuria
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
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
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
50877	neuraminidase 3	Neu3	Mus musculus (house mouse)
50935	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6	St6galnac6	Mus musculus (house mouse)
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
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
51005	amidohydrolase domain containing 2	AMDHD2 Aliases: CGI-14 N-acetylglucosamine-6-phosphate deacetylase	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
51006	solute carrier family 35 member C2	SLC35C2 Aliases: CGI-15 bA394O2.1	Homo sapiens (human)
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
51071	deoxyribose-phosphate aldolase	DERA Aliases: CGI-26 DEOC	Homo sapiens (human)	breast cancer breast carcinoma dysplastic nevus syndrome glaucoma melanoma skin melanoma
51084	crystallin lambda 1	CRYL1 Aliases: GDH L-gulonate 3-dehydrogenase MGC149525 MGC149526 crystallin, lamda 1 lambda-CRY lambda-crystallin homolog	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 Laron syndrome Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Zollinger-Ellison syndrome achondroplasia acquired thrombocytopenia acute biphenotypic leukemia acute leukemia acute myeloid leukemia autoimmune disease autoimmune lymphoproliferative syndrome beta thalassemia breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cerebral degeneration cholangiocarcinoma diabetes insipidus diarrhea embryoma giardiasis hepatocellular carcinoma hyperinsulinism hypoglycemia immune system disease intrahepatic cholangiocarcinoma liver cancer liver carcinoma mood disorder neurohypophyseal diabetes insipidus perinatal necrotizing enterocolitis placental insufficiency primary hyperoxaluria prostate cancer prostate carcinoma thalassemia
51102	mitochondrial trans-2-enoyl-CoA reductase	MECR Aliases: CGI-63 ETR1 FASN2B NRBF1 mitochondrial 2-enoyl thioester reductase nuclear receptor binding factor 1	Homo sapiens (human)	Leber hereditary optic neuropathy with demyelinating disease of CNS Unverricht-Lundborg syndrome blepharospasm blindness cerebral palsy childhood-onset dystonia with optic atrophy and basal ganglia abnormalities choreatic disease colorectal cancer colorectal carcinoma congenital nystagmus disorder of sexual development dissociated nystagmus dystonia early myoclonic encephalopathy focal hand dystonia generalized dystonia hemiplegia hermaphroditism large intestine cancer lingual-facial-buccal dyskinesia optic atrophy pathologic nystagmus pseudohermaphroditism schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus syndromic X-linked intellectual disability type 10
51144	hydroxysteroid 17-beta dehydrogenase 12	HSD17B12 Aliases: 3-ketoacyl-CoA reductase KAR SDR12C1 short chain dehydrogenase/reductase family 12C, member 1	Homo sapiens (human)	breast cancer breast carcinoma cancer carcinoma cardiovascular system disease diabetes mellitus disease of mental health embryoma head and neck squamous cell carcinoma heart disease idiopathic scoliosis intellectual disability invasive ductal carcinoma learning disability melanoma neuroblastoma obesity ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma psychotic disorder sarcomatoid carcinoma schizophrenia skin melanoma type 2 diabetes mellitus
51146	alpha-1,4-N-acetylglucosaminyltransferase	A4GNT Aliases: alpha4GnT	Homo sapiens (human)	adenocarcinoma adenoma cancer cribriform carcinoma embryoma gastric adenocarcinoma gastritis granular cell carcinoma pancreatic cancer pancreatic carcinoma peptic ulcer disease stomach cancer stomach carcinoma tubular adenocarcinoma
51148	cerebral endothelial cell adhesion molecule	CERCAM	Homo sapiens (human)
51167	cytochrome b5 reductase 4	CYB5R4 Aliases: b5+b5R dJ676J13.1	Homo sapiens (human)	breast cancer diabetes mellitus diabetic ketoacidosis gestational diabetes glucose intolerance maturity-onset diabetes of the young prediabetes syndrome type 2 diabetes mellitus
51172	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	NAGPA Aliases: APAA UCE	Homo sapiens (human)	Fabry disease alexia chylomicron retention disease dyslexia glycoproteinosis lipid storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis III mucopolysaccharidosis type IIIB neurodegenerative disease stuttering
51179	hydroxyacid oxidase 2	HAO2 Aliases: (S)-2-hydroxy-acid oxidase GIG16 HAOX2 glycolate oxidase growth-inhibiting protein 16 long-chain L-2-hydroxy acid oxidase	Homo sapiens (human)	cancer cholestasis chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 hepatocellular carcinoma hyperinsulinemic hypoglycemia inherited metabolic disorder liver cancer nonpapillary renal cell carcinoma papillary renal cell carcinoma primary hyperoxaluria renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
51181	dicarbonyl and L-xylulose reductase	DCXR Aliases: DCR HCR2 KIDCR P34H SDR20C1 human carbonyl reductase 2 kidney dicarbonyl reductase short chain dehydrogenase/reductase family 20C, member 1 sperm surface protein P34H	Homo sapiens (human)	arthritis arthropathy cancer carcinoma hemophilia B hepatocellular carcinoma liver cancer pentosuria prostate adenocarcinoma prostate cancer prostate carcinoma renal glycosuria sarcomatoid carcinoma

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