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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 **301 - 325** of **1582** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
84302	post-GPI attachment to proteins GalNAc transferase 4	PGAP4 Aliases: MGC12992	Homo sapiens (human)
84197	protein O-mannose kinase	POMK Aliases: FLJ23356 SgK196	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia blindness cardiomyopathy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly lung small cell carcinoma mechanical strabismus megalocornea microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type C12 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopia obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly strabismus syndromic X-linked intellectual disability Najm type visual epilepsy
84188	fatty acyl-CoA reductase 1	FAR1 Aliases: FLJ22728 SDR10E1 short chain dehydrogenase/reductase family 10E, member 1	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome dermatitis hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia microcephaly rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata rhizomelic chondrodysplasia punctate type 4
84076	transketolase like 2	TKTL2 Aliases: DKFZP434L1717 FLJ32975 similar to transketolase	Homo sapiens (human)	cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetes mellitus diabetic ketoacidosis embryoma hepatocellular carcinoma large intestine cancer liver cancer type 2 diabetes mellitus
84002	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5	B3GNT5 Aliases: B3GN-T5 beta3Gn-T5 lactosylceramide 1,3-N-acetyl-beta-D-glucosaminyltransferase	Homo sapiens (human)	breast cancer breast carcinoma giant cell glioblastoma glioblastoma
83931	serine/threonine kinase 40	STK40	Homo sapiens (human)
83857	transmembrane O-mannosyltransferase targeting cadherins 1	TMTC1 Aliases: ARG99 FLJ31400 FLJ41625 OLF	Homo sapiens (human)	bipolar disorder bone marrow disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma disease of mental health endometrial cancer endometrial carcinoma large intestine cancer psychotic disorder schizophrenia spinal cord disease syringomyelia
83666	poly(ADP-ribose) polymerase family member 9	PARP9 Aliases: ARTD9 BAL BAL1	Homo sapiens (human)	B-cell lymphoma Bloch-Sulzberger syndrome Gilles de la Tourette syndrome Goodpasture syndrome Loeffler syndrome Richter's syndrome Takayasu's arteritis X-linked chronic granulomatous disease acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome agranulocytosis alcohol dependence alcohol use disorder allergic asthma anorexia nervosa asthma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease bipolar disorder brain disease breast cancer breast carcinoma bronchiectasis cancer central nervous system lymphoma childhood acute lymphocytic leukemia childhood lymphoma chronic granulomatous disease chronic lymphocytic leukemia chronic obstructive pulmonary disease complement deficiency cutaneous porphyria cystic fibrosis diffuse large B-cell lymphoma embryoma eosinophilic pneumonia epithelioid sarcoma erythropoietic protoporphyria extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue extrinsic allergic alveolitis farmer's lung gastric lymphoma giardiasis granulomatosis with polyangiitis hepatitis hepatocellular carcinoma heroin dependence hypereosinophilic syndrome hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis influenza interstitial lung disease intrinsic asthma leukopenia liver cancer lung disease lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 morphine dependence neutropenia newborn respiratory distress syndrome obesity obsolete ymphosarcoma opiate dependence pneumocystosis pneumonia polyarteritis nodosa postinflammatory pulmonary fibrosis primary ciliary dyskinesia 1 primary ciliary dyskinesia prostate cancer prostate carcinoma pulmonary alveolar proteinosis pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis red-green color blindness rheumatoid arthritis sarcoidosis sarcoma schizophrenia scleroderma severe congenital neutropenia spindle cell sarcoma substance abuse substance-related disorder systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic scleroderma tuberculosis tuberculous pneumothorax uveoparotid fever
83650	solute carrier family 35 member G5	SLC35G5	Homo sapiens (human)
83639	testis expressed 101	TEX101 Aliases: CT131 MGC4766 SGRG SPATA44 TES101-reactive protein TES101RP cancer/testis antigen 131 spermatogenesis associated 44	Homo sapiens (human)	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 adenocarcinoma adenoma azoospermia basal cell carcinoma breast cancer breast ductal carcinoma cancer cribriform carcinoma embryoma granular cell carcinoma hepatocellular carcinoma liver cancer oligospermia tubular adenocarcinoma
83548	component of oligomeric golgi complex 3	COG3 Aliases: SEC34	Homo sapiens (human)	autosomal recessive limb-girdle muscular dystrophy type 2A breast cancer cancer congenital disorder of glycosylation type II
83539	carbohydrate sulfotransferase 9	CHST9 Aliases: GALNAC-4-ST2 GALNAC4ST-2	Homo sapiens (human)	acute lymphoblastic leukemia acute myeloid leukemia breast cancer breast carcinoma cancer coronary artery disease depressive disorder essential thrombocythemia hematologic cancer idiopathic scoliosis lymphoblastic lymphoma major depressive disorder melancholic depression myelodysplastic syndrome obsolete melancholia schizophrenia
83468	glycosyltransferase 8 domain containing 2	GLT8D2 Aliases: FLJ31494	Homo sapiens (human)	hepatitis C liver cirrhosis
83440	ADP dependent glucokinase	ADPGK Aliases: ADP-GK DKFZp434B195	Homo sapiens (human)
83401	ELOVL fatty acid elongase 3	ELOVL3 Aliases: CIG-30	Homo sapiens (human)	amnestic disorder atopic dermatitis dermatitis diabetes mellitus diabetic ketoacidosis ichthyosis prostate cancer prostate carcinoma retrograde amnesia type 2 diabetes mellitus
81890	queuine tRNA-ribosyltransferase catalytic subunit 1	QTRT1 Aliases: TGT tRNA-guanine transglycosylase	Homo sapiens (human)	IgA glomerulonephritis acute pancreatitis breast cancer bronchus cancer bronchus carcinoma cancer carcinoma cerebral infarction cerebrovascular disease essential thrombocythemia functionless pituitary adenoma hepatocellular carcinoma liver angiosarcoma liver cancer lung benign neoplasm lung cancer lung carcinoma multiple sclerosis myotonic dystrophy type 2 pancreatitis parapsoriasis parietal foramina prolactinoma psoriasis pulmonary embolism pustulosis of palm and sole sarcomatoid carcinoma split hand-foot malformation 1 split hand-foot malformation 2 split hand-foot malformation 3 split hand-foot malformation 4 split hand-foot malformation 5 split hand-foot malformation 6 split hand-foot malformation
81888	hydroxypyruvate isomerase (putative)	HYI Aliases: HT036	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 Pick's disease Reye syndrome cerebral degeneration
81849	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5	ST6GALNAC5 Aliases: MGC3184 ST6GalNAcV	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis breast cancer cancer central nervous system cancer central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ coronary artery disease embryoma gliosarcoma high grade glioma lymphoma mixed glioma nutmeg liver obsolete ymphosarcoma rheumatoid arthritis
81793	toll like receptor 10	TLR10	Homo sapiens (human)	asthma
81616	acyl-CoA synthetase bubblegum family member 2	ACSBG2 Aliases: BGR DKFZp434K1635 PRTD-NY3 bubblegum related protein	Homo sapiens (human)	adrenoleukodystrophy male infertility tuberculosis
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
81562	lectin, mannose binding 2 like	LMAN2L Aliases: DKFZp564L2423 VIP36-like VIPL	Homo sapiens (human)	agnosia attention deficit hyperactivity disorder autosomal dominant intellectual developmental disorder autosomal recessive intellectual developmental disorder 52 bipolar disorder borderline personality disorder cerebral degeneration choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy intermittent explosive disorder lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia papillary adenocarcinoma papillary renal cell carcinoma partial motor epilepsy pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 thyroid gland papillary carcinoma visual epilepsy
81544	glycerophosphodiester phosphodiesterase domain containing 5	GDPD5 Aliases: GDE2 PP1665	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer neuroblastoma neurodegenerative disease rheumatoid arthritis
81537	sphingosine-1-phosphate phosphatase 1	SGPP1	Homo sapiens (human)	adult lymphoma cancer colitis embryoma gastroenteritis ileitis ileocolitis inflammatory bowel disease squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma
81490	phosphatidylserine synthase 2	PTDSS2 Aliases: PSS2	Homo sapiens (human)

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