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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 **1751 - 1775** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
42380	Heparan sulfate 6-O-sulfotransferase	Hs6st	Drosophila melanogaster (fruit fly)	Paganini-Miozzo syndrome hypogonadotropic hypogonadism 15 with or without anosmia
90161	heparan sulfate 6-O-sulfotransferase 2	HS6ST2 Aliases: HS6ST-2	Homo sapiens (human)	Paganini-Miozzo syndrome arthritis arthropathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intellectual disability learning disability lung adenocarcinoma lung cancer myopia osteoarthritis stomach cancer stomach carcinoma
443852	protein phosphatase 1, catalytic subunit, beta isozyme L homeolog	ppp1cb.L	Xenopus laevis (African clawed frog)	Noonan syndrome-like disorder with loose anagen hair 2
108717671	protein phosphatase 1, catalytic subunit, beta isozyme S homeolog	ppp1cb.S	Xenopus laevis (African clawed frog)	Noonan syndrome-like disorder with loose anagen hair 2
25594	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Rattus norvegicus (Norway rat)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
19046	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Mus musculus (house mouse)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
5500	protein phosphatase 1 catalytic subunit beta	PPP1CB	Homo sapiens (human)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
496958	protein phosphatase 1, catalytic subunit, beta isozyme	ppp1cb	Xenopus tropicalis (tropical clawed frog)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
856870	type 1 serine/threonine-protein phosphatase catalytic subunit GLC7	GLC7	Saccharomyces cerevisiae S288C	Noonan syndrome-like disorder with loose anagen hair 2 cancer congestive heart failure type 2 diabetes mellitus
23423	transmembrane p24 trafficking protein 3	TMED3 Aliases: p24B p24g4 p24gamma4	Homo sapiens (human)	Nijmegen breakage syndrome anemia bacterial sepsis breast cancer breast carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy fundus albipunctatus hepatocellular carcinoma large intestine cancer liver cancer macrocytic anemia nonpapillary renal cell carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinitis pigmentosa sarcomatoid renal cell carcinoma
10924	sphingomyelin phosphodiesterase acid like 3A	SMPDL3A Aliases: ASM3A ASML3a FLJ20177 acid sphingomyelinase-like phosphodiesterase 3a yR36GH4.1	Homo sapiens (human)	Niemann-Pick disease endometriosis of ovary endometriosis of uterus endometriosis sphingolipidosis urinary bladder cancer
18145	NPC intracellular cholesterol transporter 1	Npc1	Mus musculus (house mouse)	Niemann-Pick disease type C1 Niemann-Pick disease
4864	NPC intracellular cholesterol transporter 1	NPC1 Aliases: SLC65A1	Homo sapiens (human)	Niemann-Pick disease type C1 Niemann-Pick disease
20597	sphingomyelin phosphodiesterase 1, acid lysosomal	Smpd1	Mus musculus (house mouse)	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
174131	Sphingomyelin phosphodiesterase 1	asm-1	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
176879	Putative sphingomyelin phosphodiesterase asm-3;Sphingomyelin phosphodiesterase	asm-3	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
181323	Sphingomyelin phosphodiesterase 2	asm-2	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
64772	endo-beta-N-acetylglucosaminidase	ENGASE Aliases: Di-N-acetylchitobiosyl beta-N-acetylglucosaminidase FLJ21865 Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase	Homo sapiens (human)	NGLY1-deficiency breast cancer breast carcinoma rheumatoid arthritis
56963	repulsive guidance molecule BMP co-receptor a	RGMA Aliases: RGM	Homo sapiens (human)	Mycobacterium avium complex disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease basal cell carcinoma breast cancer bronchiectasis cancer chronic fatigue syndrome chronic kidney disease complex partial epilepsy cone-rod dystrophy 2 cone-rod dystrophy cystic fibrosis disease of mental health embryoma encephalitis encephalomyelitis epilepsy hemochromatosis type 2 hemochromatosis type 2A hemochromatosis heroin dependence lesion of sciatic nerve lung disease middle cerebral artery infarction morphine dependence multiple sclerosis myelitis neuromyelitis optica obesity opiate dependence primary progressive multiple sclerosis progressive relapsing multiple sclerosis prostate cancer prostate carcinoma psychotic disorder sciatic neuropathy secondary progressive multiple sclerosis temporal lobe epilepsy visual epilepsy
27293	sphingomyelin phosphodiesterase acid like 3B	SMPDL3B Aliases: ASML3B	Homo sapiens (human)	Moyamoya disease focal segmental glomerulosclerosis glomerulonephritis kidney disease nephritis nephrosis pyoureter
26903	dysferlin	Dysf	Mus musculus (house mouse)	Miyoshi muscular dystrophy 1 autosomal recessive limb-girdle muscular dystrophy type 2B distal myopathy with anterior tibial onset distal myopathy limb-girdle muscular dystrophy muscular dystrophy
37028	acyl-CoA oxidase 1	ACOX1	Drosophila melanogaster (fruit fly)	Mitchell syndrome obesity peroxisomal acyl-CoA oxidase deficiency peroxisomal disease steatotic liver disease
51	acyl-CoA oxidase 1	ACOX1 Aliases: PALMCOX palmitoyl-CoA oxidase	Homo sapiens (human)	Mitchell syndrome X-linked nonsyndromic deafness abdominal obesity-metabolic syndrome 1 adult lymphoma anodontia 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 cancer central nervous system lymphoma cerebral infarction cerebrovascular disease childhood lymphoma citrullinemia colorectal cancer colorectal carcinoma cone-rod dystrophy congenital nystagmus craniosynostosis depressive disorder disease of metabolism dissociated nystagmus dysthymic disorder dystonia epilepsy familial hyperlipidemia fundus albipunctatus hepatocellular carcinoma hypertropia large intestine cancer leukodystrophy liver cancer liver carcinoma lymphoma major depressive disorder mechanical strabismus melancholic depression mitochondrial metabolism disease mitochondrial myopathy myopia neurodegenerative disease neurotic disorder obesity obsolete autosomal recessive nonsyndromic deafness 105 obsolete melancholia obsolete ymphosarcoma ophthalmoplegia optic atrophy pathologic nystagmus peroxisomal acyl-CoA oxidase deficiency peroxisomal disease retinitis pigmentosa sensorineural hearing loss speech disorder spontaneous ocular nystagmus steatotic liver disease strabismus syndromic X-linked intellectual disability 94 tooth agenesis visual epilepsy
56953	5',3'-nucleotidase, mitochondrial	NT5M Aliases: dNT-2 dNT2 mdN	Homo sapiens (human)	Miller-Dieker lissencephaly syndrome Smith-Magenis syndrome
114780	polycystin 1 like 2 (gene/pseudogene)	PKD1L2 Aliases: KIAA1879	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease

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