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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 **476 - 500** of **1582** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
55650	phosphatidylinositol glycan anchor biosynthesis class V	PIGV Aliases: FLJ20477 GPI mannosyltransferase 2 GPI-MT-II PIG-V dol-P-Man dependent GPI mannosyltransferase II	Homo sapiens (human)	Cogan syndrome Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome anorectal stricture blepharospasm capillary disease congenital heart disease craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 1 intellectual disability learning disability monocular esotropia oligohydramnios pyridoxine deficiency anemia scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis visual epilepsy
55627	sphingomyelin phosphodiesterase 4	SMPD4 Aliases: FLJ20297 FLJ20756 KIAA1418 NET13 NSMASE3 nSMase-3 neutral sphingomyelinase-3	Homo sapiens (human)	acute myocardial infarction coronary thrombosis microcephaly myocardial infarction silent myocardial infarction
55624	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	POMGNT1 Aliases: FLJ20277 LGMD2O MGAT1.2 protein O-mannose beta-1,2-N-acetylglucosaminyltransferase	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Unverricht-Lundborg syndrome Walker-Warburg syndrome Zollinger-Ellison syndrome adult medulloblastoma agnosia autism spectrum disorder autistic disorder 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 blepharospasm blindness buphthalmos cardiomyopathy cataract centronuclear myopathy childhood medulloblastoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A3 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness congenital structural myopathy cornea plana corneal disease cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder diabetes mellitus dissociated nystagmus distal myopathy early myoclonic encephalopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal hand dystonia fundus albipunctatus fundus dystrophy giant cell glioblastoma glaucoma glioblastoma high grade glioma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hyperinsulinism hypertrophic cardiomyopathy hypertropia hypogonadism intellectual disability isolated elevated serum creatine phosphokinase levels keratoconus learning disability limb-girdle muscular dystrophy lissencephaly mechanical strabismus medulloblastoma medullomyoblastoma megaconial type congenital muscular dystrophy megalocornea melanotic medulloblastoma meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia nemaline myopathy neuroblastoma night blindness obesity obsolete asthenopia 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 pathologic nystagmus peripheral retinal degeneration pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment retinal disease retinitis pigmentosa retinitis rigid spine muscular dystrophy 1 rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type type 2 diabetes mellitus visual epilepsy
55613	myotubularin related protein 8	MTMR8 Aliases: FLJ20126	Homo sapiens (human)	Charcot-Marie-Tooth disease breast cancer centronuclear myopathy X-linked centronuclear myopathy
55600	intelectin 1	ITLN1 Aliases: FLJ20022 HL-1 ITLN LFR hIntL omentin	Homo sapiens (human)	Crohn's colitis Crohn's disease adenocarcinoma adenoma allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis bacterial infectious disease benign mesothelioma cancer carcinoma coronary artery disease cribriform carcinoma dermatitis diabetes mellitus diabetic ketoacidosis granular cell carcinoma inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma malignant epithelial mesothelioma malignant mesothelioma multiple sclerosis neuroblastoma nutmeg liver obesity osteoporosis parapsoriasis pneumonia polycystic ovary syndrome primary biliary cholangitis psoriasis pustulosis of palm and sole sarcomatoid carcinoma stomach cancer stomach carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis
55586	myo-inositol oxygenase	MIOX Aliases: kidney-specific protein 32	Homo sapiens (human)	cryptococcosis diabetes mellitus diabetic ketoacidosis obesity obsolete type 1 diabetes mellitus 9 polycystic ovary syndrome steatotic liver disease type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus
55577	N-acetylglucosamine kinase	NAGK	Homo sapiens (human)	prostate cancer prostate carcinoma
55568	polypeptide N-acetylgalactosaminyltransferase 10	GALNT10 Aliases: GalNAc-T10 polypeptide GalNAc transferase 10	Homo sapiens (human)	hepatitis B hepatocellular carcinoma liver cancer schizophrenia
55556	enolase superfamily member 1	ENOSF1 Aliases: FUCD HSRTSBETA L-fuconate dehydratase TYMSAS rTS	Homo sapiens (human)	Down syndrome Hailey-Hailey disease Holt-Oram syndrome Klippel-Trenaunay syndrome Marfan syndrome Plasmodium falciparum malaria Rothmund-Thomson syndrome Rubinstein-Taybi syndrome VACTERL association Werner syndrome adult lymphoma arachnoiditis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB cancer central nervous system cancer central nervous system lymphoma cerebral malaria childhood leukemia childhood lymphoma colorectal cancer colorectal carcinoma congenital central hypoventilation syndrome cutaneous mastocytosis cutis laxa diffuse cutaneous mastocytosis embryoma endometrial cancer endometrial carcinoma exanthem gliosarcoma hepatitis B herpes zoster high grade glioma intellectual disability large intestine cancer learning disability leukemia lymphoma mal de Meleda malaria mastocytosis meningitis microphthalmia with limb anomalies mixed glioma mixed sleep apnea nail-patella syndrome obsolete ymphosarcoma obstructive sleep apnea ovarian cancer ovarian carcinoma poikiloderma with neutropenia progeria rabies restrictive dermopathy situs inversus sleep apnea split hand-foot malformation 1 with sensorineural hearing loss stomach cancer stomach carcinoma thrombocytopenia-absent radius syndrome tuberous sclerosis urticaria pigmentosa uterine corpus cancer
55526	dehydrogenase E1 and transketolase domain containing 1	DHTKD1	Homo sapiens (human)	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
55512	sphingomyelin phosphodiesterase 3	SMPD3 Aliases: NSMASE2 neutral sphingomyelinase II	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 Ehlers-Danlos syndrome Guillain-Barre syndrome Kallmann syndrome Laron syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sheehan syndrome Zika fever achondroplasia acute myeloid leukemia acute pericementitis aggressive periodontitis alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer breast carcinoma cancer central nervous system disease cerebral degeneration chronic kidney disease chronic obstructive pulmonary disease coronary artery disease embryoma essential thrombocythemia hepatocellular carcinoma hyperphosphatemia 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 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 leprosy leukemia liver cancer lymphoid leukemia microcephaly myelodysplastic syndrome myeloid leukemia nervous system disease osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta panhypopituitarism periodontosis primary pulmonary hypertension pulmonary emphysema pulmonary hypertension schizophrenia thymus gland disease transient cerebral ischemia vertebrobasilar insufficiency
55508	solute carrier family 35 member E3	SLC35E3 Aliases: BLOV1	Homo sapiens (human)	cardiovascular system disease heart disease
55501	carbohydrate sulfotransferase 12	CHST12 Aliases: C4S-2 C4ST2 chondroitin 4-sulfotransferase 2	Homo sapiens (human)	hypertension lupus erythematosus systemic lupus erythematosus
55500	ethanolamine kinase 1	ETNK1 Aliases: EKI EKI1	Homo sapiens (human)	aggressive systemic mastocytosis atypical chronic myeloid leukemia, BCR-ABL1 negative cancer chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia disseminated eosinophilic collagen disease epilepsy heart conduction disease hypereosinophilic syndrome indolent systemic mastocytosis juvenile myelomonocytic leukemia mastocytosis microcephaly myeloid leukemia obsolete subacute myeloid leukemia seminoma systemic mastocytosis testicular cancer testicular germ cell cancer testis seminoma
55454	chondroitin sulfate N-acetylgalactosaminyltransferase 2	CSGALNACT2 Aliases: GALNACT-2 GALNACT2 MGC40204 PRO0082 chondroitin beta1,4 N-acetylgalactosaminyltransferase 2 glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase 2	Homo sapiens (human)	Hirschsprung's disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis multiple sclerosis
55361	phosphatidylinositol 4-kinase type 2 alpha	PI4K2A Aliases: DKFZP761G1923 PI4KII PIK42A	Homo sapiens (human)	Hermansky-Pudlak syndrome breast cancer cancer embryoma giant cell glioblastoma glioblastoma
55347	abhydrolase domain containing 10, depalmitoylase	ABHD10 Aliases: FLJ11342 Mycophenolic acid acyl-glucuronide esterase, mitochondrial	Homo sapiens (human)
55343	solute carrier family 35 member C1	SLC35C1 Aliases: FLJ11320 FUCT1 GDP-fucose transporter 1	Homo sapiens (human)	Laron syndrome achondroplasia anxiety disorder cellulitis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc echolalia generalized anxiety disorder hepatocellular carcinoma leukocyte adhesion deficiency 2 leukocyte adhesion deficiency liver cancer microcephaly
55331	alkaline ceramidase 3	ACER3 Aliases: APHC FLJ11238 alkaline phytoceramidase	Homo sapiens (human)	Cauda equina syndrome Laron syndrome achondroplasia acute myeloid leukemia cerebellar ataxia cerebellar disease cerebral degeneration dystonia hepatocellular carcinoma intellectual disability learning disability leukodystrophy liver cancer melanoma metabolic dysfunction-associated steatohepatitis neurogenic bladder neuropathy peripheral nervous system disease skin melanoma
55326	1-acylglycerol-3-phosphate O-acyltransferase 5	AGPAT5 Aliases: 1-acyl-sn-glycerol-3-phosphate acyltransferase epsilon FLJ11210 LPAAT-e LPAAT-epsilon LPLAT5 lysophosphatidic acid acyltransferase, epsilon lysophospholipid acyltransferase 5	Homo sapiens (human)
55304	serine palmitoyltransferase long chain base subunit 3	SPTLC3 Aliases: FLJ11112 LCB2B hLCB2b	Homo sapiens (human)	autosomal dominant cerebellar ataxia bacterial sepsis head and neck squamous cell carcinoma hereditary sensory and autonomic neuropathy type 1 neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy sensory peripheral neuropathy spinocerebellar ataxia type 7
55301	oleoyl-ACP hydrolase	OLAH Aliases: FLJ11106 S-acyl fatty acid synthase thioesterase, medium chain SAST oleoyl-acyl-carrier-protein hydrolase	Homo sapiens (human)	migraine
55300	phosphatidylinositol 4-kinase type 2 beta	PI4K2B Aliases: FLJ11105 PI4KIIB PIK42B	Homo sapiens (human)	attention deficit hyperactivity disorder bipolar disorder childhood leukemia chronic myeloid leukemia disease of mental health leukemia psychotic disorder schizophrenia
55277	FGGY carbohydrate kinase domain containing	FGGY	Homo sapiens (human)
55276	phosphoglucomutase 2	PGM2 Aliases: FLJ10983 phosphopentomutase	Homo sapiens (human)

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