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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 **1376 - 1400** of **1582** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
130367	sphingosine-1-phosphate phosphatase 2	SGPP2 Aliases: FLJ39004 SPP2	Homo sapiens (human)	cancer colitis embryoma gastroenteritis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease stomach cancer stomach carcinoma ulcerative colitis
130574	LY6/PLAUR domain containing 6	LYPD6 Aliases: MGC52057	Homo sapiens (human)	Gilles de la Tourette syndrome anxiety disorder generalized anxiety disorder phobic disorder
130576	LY6/PLAUR domain containing 6B	LYPD6B Aliases: CT116 LYPD7 cancer/testis antigen 116	Homo sapiens (human)
130589	galactose mutarotase	GALM Aliases: aldose 1-epimerase aldose mutarotase galactomutarotase	Homo sapiens (human)	Crohn's colitis Crohn's disease classic galactosemia colitis colorectal cancer colorectal carcinoma galactokinase deficiency galactosemia gastroenteritis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease 2 inflammatory bowel disease large intestine cancer ulcerative colitis
130749	carboxypeptidase O	CPO Aliases: metallocarboxypeptidase C metallocarboxypeptidase O	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 DiGeorge syndrome Pick's disease Reye syndrome Van der Woude syndrome cerebral degeneration colorectal cancer colorectal carcinoma craniosynostosis hereditary coproporphyria large intestine cancer melorheostosis velocardiofacial syndrome
131375	lysozyme like 4	LYZL4 Aliases: LYC4 MGC26768	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
131544	crystallin beta-gamma domain containing 3	CRYBG3 Aliases: DKFZp667G2110	Homo sapiens (human)	bronchus cancer bronchus carcinoma cancer embryoma lung cancer lung carcinoma
132158	glycerate kinase	GLYCTK Aliases: HBEBP2 HBEBP4	Homo sapiens (human)	D-glyceric aciduria Unverricht-Lundborg syndrome blepharospasm brain disease early myoclonic encephalopathy epilepsy focal hand dystonia glycine encephalopathy intellectual disability lactic acidosis learning disability locked-in syndrome microcephaly obsolete infantile epileptic encephalopathy primary hyperoxaluria quadriplegia schizophrenia visual epilepsy
132789	glucosamine-6-phosphate deaminase 2	GNPDA2 Aliases: SB52 glucosamine-6-phosphate isomerase	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 Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 allergic asthma asthma cardiovascular system disease cerebral degeneration diabetes mellitus essential hypertension heart disease hypertension intrinsic asthma obesity type 2 diabetes mellitus
133121	ectonucleotide pyrophosphatase/phosphodiesterase 6	ENPP6 Aliases: MGC33971	Homo sapiens (human)
133688	UDP glycosyltransferase family 3 member A1	UGT3A1 Aliases: FLJ34658	Homo sapiens (human)
134526	acyl-CoA thioesterase 12	ACOT12 Aliases: Cach STARD15 StAR-related lipid transfer (START) domain containing 15 THEAL	Homo sapiens (human)	hepatocellular carcinoma leukodystrophy leukoencephalopathy with vanishing white matter liver cancer
135152	beta-1,3-glucuronyltransferase 2	B3GAT2 Aliases: GlcAT-S galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2 glucuronosyltransferase S	Homo sapiens (human)	Barrett's esophagus schizophrenia thrombophilia
135228	CD109 molecule	CD109 Aliases: CPAMD7 DKFZp762L1111 FLJ38569	Homo sapiens (human)	Fukuyama congenital muscular dystrophy Marfan syndrome X-linked nonsyndromic deafness acrodermatitis adenocarcinoma adenoma adult epithelioid sarcoma amyloidosis autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness blindness bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral palsy cervical squamous cell carcinoma childhood epithelioid sarcoma childhood osteosarcoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis diffuse large B-cell lymphoma embryoma endometrial adenocarcinoma epithelioid sarcoma familial periodic paralysis gallbladder squamous cell carcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer hemiplegia hepatocellular carcinoma high grade glioma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma mixed glioma multiple endocrine neoplasia type 1 myopathy obsolete autosomal recessive nonsyndromic deafness 105 osteosarcoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma penis squamous cell carcinoma prostate cancer prostate carcinoma rheumatoid arthritis sarcoma sarcomatoid carcinoma situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell sarcoma squamous cell carcinoma tongue squamous cell carcinoma tuberous sclerosis tubular adenocarcinoma
137797	LY6/PLAUR domain containing 2	LYPD2 Aliases: RGTR430 UNQ430	Homo sapiens (human)
137964	glycerol-3-phosphate acyltransferase 4	GPAT4 Aliases: DKFZp586M1819 LPAAT-zeta TSARG7 lysophosphatidic acid acyltransferase, zeta	Homo sapiens (human)	diabetes mellitus type 2 diabetes mellitus
138050	heparan-alpha-glucosaminide N-acetyltransferase	HGSNAT Aliases: FLJ32731 HGNAT	Homo sapiens (human)	Zollinger-Ellison syndrome agnosia amnestic disorder blindness bulimia nervosa cataract cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease developmental coordination disorder diabetes mellitus diarrhea dissociated nystagmus echolalia enterocele epilepsy fundus albipunctatus fundus dystrophy glaucoma hyperinsulinism hypertrichosis hypertrophic cardiomyopathy 1 hypogonadism intellectual disability keratoconus learning disability mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis night blindness obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus peripheral retinal degeneration retinitis pigmentosa 73 retinitis pigmentosa retrograde amnesia scoliosis sensorineural hearing loss spontaneous ocular nystagmus stereotypic movement disorder type 2 diabetes mellitus visual epilepsy
138429	phosphatidylinositol-4-phosphate 5-kinase like 1	PIP5KL1 Aliases: MGC46424 bA203J24.5	Homo sapiens (human)	cancer cervical cancer cervix carcinoma embryoma stomach cancer stomach carcinoma in situ stomach carcinoma
139189	diacylglycerol kinase kappa	DGKK	Homo sapiens (human)	Marfan syndrome agnosia arteriosclerotic cardiovascular disease atherosclerosis conduct disorder coronary artery disease developmental coordination disorder disease of mental health fragile X syndrome hepatocellular carcinoma hypospadias liver cancer prostate cancer prostate carcinoma situs inversus syndromic X-linked intellectual disability 94 tuberous sclerosis
140578	chondrolectin	CHODL Aliases: FLJ12627 MT75 PRED12	Homo sapiens (human)	bronchus cancer bronchus carcinoma bulimia nervosa cancer idiopathic scoliosis lung cancer lung carcinoma lung non-small cell carcinoma progressive muscular atrophy spinal muscular atrophy
140687	glucosaminyl (N-acetyl) transferase family member 7	GCNT7 Aliases: dJ1153D9.2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
140733	mono-ADP ribosylhydrolase 2	MACROD2 Aliases: O-acetyl-ADP-ribose deacetylase MACROD2 dJ631M13.5	Homo sapiens (human)	Crohn's colitis Crohn's disease Kabuki syndrome acquired immunodeficiency syndrome acute myeloid leukemia autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma disease of mental health embryoma essential hypertension hepatocellular carcinoma human immunodeficiency virus infectious disease hypertension hypogonadotropic hypogonadism 21 with or without anosmia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability large intestine cancer learning disability liver cancer malignant fibrous histiocytoma obesity psychotic disorder substance abuse substance-related disorder ulcerative colitis
140838	N-acetylneuraminic acid phosphatase	NANP Aliases: MGC26833 dJ694B14.3	Homo sapiens (human)	cancer cerebral degeneration colorectal cancer esophageal cancer esophageal carcinoma large intestine cancer malaria
140873	chromosome 20 open reading frame 173	C20orf173 Aliases: dJ477O4.4	Homo sapiens (human)
142683	intelectin 2	ITLN2 Aliases: HL-2	Homo sapiens (human)

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