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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 **1851 - 1875** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
100490155	glycogen synthase 1	gys1	Xenopus tropicalis (tropical clawed frog)	Lafora disease cardiovascular system disease
850962	glycogen (starch) synthase GSY2	GSY2	Saccharomyces cerevisiae S288C	Lafora disease cardiovascular system disease glycogen storage disease
41823	Glycogen synthase	Glys	Drosophila melanogaster (fruit fly)	Lafora disease cardiovascular system disease glycogen storage disease
174924	Glycogen [starch] synthase	gsy-1	Caenorhabditis elegans	Lafora disease cardiovascular system disease glycogen storage disease
850569	glycogen (starch) synthase GSY1	GSY1	Saccharomyces cerevisiae S288C	Lafora disease cardiovascular system disease glycogen storage disease
79660	protein phosphatase 1 regulatory subunit 3B	PPP1R3B Aliases: FLJ14005 GL PP1 subunit R4 PPP1R4 hepatic glycogen-targeting subunit, G(L)	Homo sapiens (human)	Lafora disease alcohol use disorder antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer coronary artery disease depressive disorder diabetes mellitus dysthymic disorder embryoma head and neck cancer major depressive disorder maturity-onset diabetes of the young melancholic depression melanoma neurotic disorder obesity obsolete melancholia post-traumatic stress disorder protein C deficiency protein S deficiency skin melanoma steatotic liver disease thrombophilia type 2 diabetes mellitus
416	arylsulfatase F	ARSF Aliases: ASF	Homo sapiens (human)	Kuhnt-Junius degeneration breast cancer cancer embryoma epithelioid sarcoma hepatocellular carcinoma inflammatory bowel disease influenza liver cancer lung benign neoplasm lung cancer lung non-small cell carcinoma multiple sclerosis myositis neuroblastoma papilloma progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma sarcoma spinal muscular atrophy spindle cell sarcoma squamous cell carcinoma squamous cell papilloma stomach cancer stomach carcinoma substance abuse substance-related disorder systemic lupus erythematosus tongue squamous cell carcinoma
2528	fucosyltransferase 6	FUT6 Aliases: FCT3A FLJ40754 FT1A FucT-VI alpha-(1,3)-fucosyltransferase galactoside 3-L-fucosyltransferase	Homo sapiens (human)	Kuhnt-Junius degeneration age related macular degeneration breast cancer cancer candidiasis carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma degeneration of macula and posterior pole embryoma hepatocellular carcinoma large intestine cancer liver cancer macular degeneration pernicious anemia prostate cancer prostate carcinoma sarcomatoid carcinoma stomach cancer stomach carcinoma
81579	phospholipase A2 group XIIA	PLA2G12A	Homo sapiens (human)	Kuhnt-Junius degeneration age related macular degeneration arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder autistic disorder degeneration of macula and posterior pole macular degeneration schizophrenia
22918	CD93 molecule	CD93 Aliases: C1qR(P) C1qRP CDw93 ECSM3 dJ737E23.1	Homo sapiens (human)	Kuhnt-Junius degeneration acute leukemia acute myocardial infarction allergic asthma asthma cancer central nervous system cancer chronic fatigue syndrome coronary artery disease coronary thrombosis embryoma encephalitis encephalomyelitis giant cell glioblastoma glioblastoma gliosarcoma high grade glioma intrinsic asthma lung cancer lung non-small cell carcinoma mixed glioma myelitis myocardial infarction nasopharynx carcinoma parapsoriasis psoriasis pustulosis of palm and sole silent myocardial infarction thyroid gland carcinoma vascular cancer
6785	ELOVL fatty acid elongase 4	ELOVL4 Aliases: CT118 cancer/testis antigen 118	Homo sapiens (human)	Kuhnt-Junius degeneration Leber congenital amaurosis Sjogren-Larsson syndrome Stargardt disease achromatopsia acquired color blindness acquired hyperkeratosis acute myocardial infarction age related macular degeneration alternating hemiplegia of childhood angioedema anhidrosis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis blindness blue color blindness cancer cardiac arrest central nervous system disease cerebellar ataxia cerebellar disease color blindness cone-rod dystrophy 2 cone-rod dystrophy 7 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal dystrophy coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis dissociated nystagmus dry eye syndrome epilepsy erythrokeratodermia variabilis et progressiva 1 erythrokeratodermia variabilis eye disease fundus albipunctatus glycogen storage disease II granuloma annulare hepatocellular carcinoma hypertropia hypohidrosis ichthyosis inguinal hernia keratosis follicularis liver cancer locked-in syndrome macular degeneration mechanical strabismus mongolian spot myocardial infarction nervous system disease neurodegenerative disease night blindness obsolete congenital ichthyosiform erythroderma ophthalmoplegia pathologic nystagmus pseudoxanthoma elasticum quadriplegia red color blindness red-green color blindness retinitis pigmentosa 25 retinitis pigmentosa 30 retinitis pigmentosa silent myocardial infarction skin disease spinocerebellar ataxia type 34 spontaneous ocular nystagmus strabismus thrombocytopenia type 2 diabetes mellitus urticaria visual epilepsy xerophthalmia
3955	LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	LFNG Aliases: SCDO3	Homo sapiens (human)	Klippel-Feil syndrome Laron syndrome Marfan syndrome achondroplasia breast cancer breast carcinoma cleft palate congenital diaphragmatic hernia cryptorchidism dysostosis hypospadias inguinal hernia intellectual disability isolated cleft palate learning disability meningocele microcephaly mucopolysaccharidosis IV multiple epiphyseal dysplasia omphalocele osteochondrodysplasia pancreatic cancer pancreatic carcinoma placental insufficiency scimitar syndrome scoliosis sickle cell anemia situs inversus spina bifida occulta spondylocostal dysostosis 3 spondylocostal dysostosis spondylolisthesis systemic primary carnitine deficiency disease tuberous sclerosis umbilical hernia
39596	dally-like	dlp	Drosophila melanogaster (fruit fly)	Keipert syndrome hepatocellular carcinoma omodysplasia 1
80255	solute carrier family 35 member F5	SLC35F5 Aliases: FLJ22004	Homo sapiens (human)	Kawasaki disease cancer
266727	MAM domain containing glycosylphosphatidylinositol anchor 1	MDGA1 Aliases: GPIM MAMDC3	Homo sapiens (human)	Kawasaki disease bipolar disorder cancer depressive disorder major depressive disorder melancholic depression neurotic disorder obsolete melancholia schizophrenia
25459	high mobility group box 1	Hmgb1	Rattus norvegicus (Norway rat)	Kawasaki disease amyotrophic lateral sclerosis atherosclerosis brain infarction cerebral infarction colon adenocarcinoma congestive heart failure high grade glioma hydrocephalus middle cerebral artery infarction myocardial infarction obstructive jaundice periodontitis pulmonary hypertension sciatic neuropathy systemic scleroderma
15289	high mobility group box 1	Hmgb1	Mus musculus (house mouse)	Kawasaki disease amyotrophic lateral sclerosis atherosclerosis brain infarction cerebral infarction colon adenocarcinoma congestive heart failure high grade glioma hydrocephalus middle cerebral artery infarction myocardial infarction obstructive jaundice periodontitis pulmonary hypertension sciatic neuropathy systemic scleroderma
93978	C-type lectin domain containing 6A	CLEC6A Aliases: dectin-2 hDECTIN-2	Homo sapiens (human)	Kawasaki disease acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer candidiasis cholesteatoma coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis dermatomycosis dermatophytosis embryoma fungal infectious disease myocardial infarction pneumocystosis pneumonia polyp of middle ear rheumatoid arthritis silent myocardial infarction superficial mycosis tinea favosa tuberculosis vasculitis
253782	ceramide synthase 6	CERS6	Homo sapiens (human)	Kawasaki disease Kennedy's disease T-cell acute lymphoblastic leukemia acute lymphoblastic leukemia adult acute lymphocytic leukemia alcoholic hepatitis alcoholic liver cirrhosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood acute lymphocytic leukemia chronic fatigue syndrome colitis colorectal cancer colorectal carcinoma diabetes mellitus disease of metabolism embryoma encephalitis encephalomyelitis gastroenteritis glucose intolerance head and neck squamous cell carcinoma hematologic cancer idiopathic scoliosis ileitis ileocolitis large intestine cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma mitochondrial metabolism disease mitochondrial myopathy multiple sclerosis myelitis obesity prediabetes syndrome skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder tongue squamous cell carcinoma type 2 diabetes mellitus
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
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
9394	heparan sulfate 6-O-sulfotransferase 1	HS6ST1	Homo sapiens (human)	Kallmann syndrome Potter's syndrome Sheehan syndrome achromatopsia acquired color blindness anxiety disorder bilateral renal aplasia blindness blue color blindness cartilage-hair hypoplasia clubfoot color blindness congenital nystagmus congenital ptosis cryptorchidism depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dysthymic disorder epilepsy eunuchism generalized anxiety disorder gynecomastia hypertrophy of breast hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 15 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism ichthyosis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis impotence infant gynecomastia isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency major depressive disorder melancholic depression mucopolysaccharidosis IV multiple epiphyseal dysplasia neurotic disorder obesity obsolete melancholia osteochondrodysplasia osteoporosis panhypopituitarism paraplegia pathologic nystagmus premature ejaculation psychologic dyspareunia ptosis red color blindness red-green color blindness schizophrenia sensorineural hearing loss septooptic dysplasia spontaneous ocular nystagmus type 2 diabetes mellitus visual epilepsy
8482	semaphorin 7A (JohnMiltonHagen blood group)	SEMA7A Aliases: CD108 H-Sema K1 H-Sema-L John Milton Hagen blood group	Homo sapiens (human)	Kallmann syndrome Kaposi's sarcoma Sheehan syndrome Sjogren's syndrome St. Louis encephalitis alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy autosomal dominant polycystic kidney disease breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system disease cerebral infarction cerebrovascular disease chronic fatigue syndrome complex partial epilepsy congenital myasthenic syndrome coronary artery disease embryoma encephalitis encephalomyelitis epilepsy essential hypertension eunuchism gliosarcoma high grade glioma hypertension hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency keratoconjunctivitis sicca lung adenocarcinoma lung cancer melanoma mixed glioma multiple sclerosis myelitis nervous system disease pancreatic cancer pancreatic carcinoma panhypopituitarism pneumonia polycystic kidney disease 1 postinflammatory pulmonary fibrosis progressive familial intrahepatic cholestasis pterygium pulmonary fibrosis rheumatoid arthritis septooptic dysplasia skin melanoma systemic lupus erythematosus temporal lobe epilepsy visual epilepsy
160418	transmembrane O-mannosyltransferase targeting cadherins 3	TMTC3 Aliases: FLJ90492 SMILE	Homo sapiens (human)	Joubert syndrome Miller-Dieker lissencephaly syndrome acute myocardial infarction adult lymphoma agranulocytosis aortic aneurysm aortic valve insufficiency blood coagulation disease breast cancer breast carcinoma cancerophobia central nervous system lymphoma childhood lymphoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure coronary thrombosis cortical dysplasia-focal epilepsy syndrome dental caries dentin caries dermoid cyst of ovary dermoid cyst enterocele epilepsy focal epilepsy hydranencephaly hydrocephalus intellectual disability learning disability leukopenia lissencephaly 8 lissencephaly lung cancer lung non-small cell carcinoma lymphoma myocardial infarction myopia neutropenia obsolete malignant histiocytosis obsolete ymphosarcoma optic atrophy partial motor epilepsy periventricular nodular heterotopia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pyloric stenosis septooptic dysplasia severe congenital neutropenia short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction syndromic X-linked intellectual disability Najm type visual epilepsy
9091	phosphatidylinositol glycan anchor biosynthesis class Q	PIGQ Aliases: GPI1 Phosphatidylinositol N-acetylglucosaminyltransferase subunit Q hGPI1	Homo sapiens (human)	Joubert syndrome Miller-Dieker lissencephaly syndrome Unverricht-Lundborg syndrome West syndrome acute myocardial infarction alternating exotropia aromatase excess syndrome arthritis arthropathy 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 basal ganglia disease blepharospasm cleft palate complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital nystagmus congenital ptosis coronary thrombosis cortical dysplasia-focal epilepsy syndrome developmental and epileptic encephalopathy 1 dissociated nystagmus dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy epilepsy episodic ataxia exotropia focal hand dystonia hydranencephaly hydronephrosis hypertropia inguinal hernia intellectual disability intestinal volvulus isolated cleft palate learning disability lingual-facial-buccal dyskinesia lissencephaly mechanical strabismus microcephaly monocular exotropia multiple congenital anomalies-hypotonia-seizures syndrome 4 myocardial infarction obsolete infantile epileptic encephalopathy omphalocele ophthalmoplegia optic atrophy patent ductus arteriosus patent foramen ovale pathologic nystagmus pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary immunodeficiency disease ptosis pulmonary valve stenosis renal agenesis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability Najm type umbilical hernia ureterocele ventricular septal defect vesicoureteral reflux visual epilepsy

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