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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	October 29, 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 **6426 - 6450** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
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
55602	CDKN2A interacting protein	CDKN2AIP	Homo sapiens (human)
55605	kinesin family member 21A	KIF21A	Homo sapiens (human)
55607	protein phosphatase 1 regulatory subunit 9A	PPP1R9A	Homo sapiens (human)
55609	zinc finger protein 280C	ZNF280C	Homo sapiens (human)
55613	myotubularin related protein 8	MTMR8 Aliases: FLJ20126	Homo sapiens (human)	Charcot-Marie-Tooth disease breast cancer centronuclear myopathy X-linked centronuclear myopathy
55619	dedicator of cytokinesis 10	DOCK10	Homo sapiens (human)
55620	signal transducing adaptor family member 2	STAP2	Homo sapiens (human)
55622	tetratricopeptide repeat domain 27	TTC27	Homo sapiens (human)
55623	THUMP domain containing 1	THUMPD1	Homo sapiens (human)
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
55625	zinc finger DHHC-type palmitoyltransferase 7	ZDHHC7	Homo sapiens (human)
55626	autophagy and beclin 1 regulator 1	AMBRA1	Homo sapiens (human)
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
55628	zinc finger protein 407	ZNF407	Homo sapiens (human)
55630	solute carrier family 39 member 4	SLC39A4	Homo sapiens (human)
55631	leucine rich repeat containing 40	LRRC40	Homo sapiens (human)
55635	DEP domain containing 1	DEPDC1	Homo sapiens (human)
55636	chromodomain helicase DNA binding protein 7	CHD7	Homo sapiens (human)
55638	syntabulin	SYBU	Homo sapiens (human)
55644	O-sialoglycoprotein endopeptidase	OSGEP	Homo sapiens (human)
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
55655	NLR family pyrin domain containing 2	NLRP2	Homo sapiens (human)
55660	pre-mRNA processing factor 40 homolog A	PRPF40A	Homo sapiens (human)
55661	DEAD-box helicase 27	DDX27	Homo sapiens (human)

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