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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 **1876 - 1900** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
39404	Inositol polyphosphate 5-phosphatase E	INPP5E	Drosophila melanogaster (fruit fly)	Joubert syndrome 1 Joubert syndrome obesity
3784	potassium voltage-gated channel subfamily Q member 1	KCNQ1	Homo sapiens (human)	Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
84020	potassium voltage-gated channel subfamily Q member 1	Kcnq1	Rattus norvegicus (Norway rat)	Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
9486	carbohydrate sulfotransferase 10	CHST10 Aliases: HNK-1ST	Homo sapiens (human)	Japanese encephalitis dengue disease schizophrenia viral infectious disease yellow fever
201595	STT3 oligosaccharyltransferase complex catalytic subunit B	STT3B Aliases: Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B FLJ90106 SIMP STT3-B dolichyl-diphosphooligosaccharide protein glycotransferase source of immunodominant MHC associated peptides	Homo sapiens (human)	Japanese encephalitis congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix congenital disorder of glycosylation cryptorchidism dengue disease epilepsy intellectual disability learning disability microcephaly optic atrophy placental insufficiency sleeping sickness thrombocytopenia trypanosomiasis viral infectious disease visual epilepsy yellow fever
10554	1-acylglycerol-3-phosphate O-acyltransferase 1	AGPAT1 Aliases: 1-acyl-sn-glycerol-3-phosphate acyltransferase alpha LPAAT-alpha LPLAT1 lysophosphatidic acid acyltransferase, alpha lysophospholipid acyltransferase l	Homo sapiens (human)	Japanese encephalitis cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 dengue disease diabetic ketoacidosis embryoma lipoatrophic diabetes mellitus lipodystrophy obsolete type 1 diabetes mellitus 9 pancreatic cancer pancreatic carcinoma rheumatoid arthritis 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 viral infectious disease yellow fever
7841	mannosyl-oligosaccharide glucosidase	MOGS Aliases: CWH41 DER7 GCS1 glucosidase I processing A-glucosidase I	Homo sapiens (human)	Japanese encephalitis Turner syndrome Zika fever acquired hyperkeratosis actinic keratosis acute lymphoblastic leukemia acute myeloid leukemia adamantinoma agammaglobulinemia ameloblastoma blepharophimosis bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic monocytic leukemia chronic myelomonocytic leukemia congenital disorder of glycosylation In congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIb congenital disorder of glycosylation cystic fibrosis dengue disease epilepsy gonadal dysgenesis holoprosencephaly 1 holoprosencephaly juvenile myelomonocytic leukemia keratoacanthoma lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma malaria melanoma obesity optic atrophy pleomorphic xanthoastrocytoma sensorineural hearing loss skin melanoma viral infectious disease visual epilepsy yellow fever
23601	C-type lectin domain containing 5A	CLEC5A Aliases: MDL-1	Homo sapiens (human)	Japanese encephalitis Mycoplasma pneumoniae pneumonia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis bone osteosarcoma brain glioblastoma multiforme central nervous system cancer cholesteatoma dengue disease dengue hemorrhagic fever giant cell glioblastoma glioblastoma gliosarcoma high grade glioma mixed glioma osteoarthritis osteosarcoma polyp of middle ear viral infectious disease yellow fever
1650	dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit	DDOST Aliases: KIAA0115 OST OST48 WBP1 advanced glycation end-product receptor 1 oligosaccharyltransferase subunit 48	Homo sapiens (human)	Japanese encephalitis Laron syndrome achondroplasia animal phobia blood coagulation disease bone osteosarcoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma chronic kidney disease congenital disorder of glycosylation Ir congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 dengue disease diabetes mellitus diabetic ketoacidosis epilepsy esophagitis esotropia gastroesophageal reflux disease glomerulonephritis glucose intolerance hepatitis C hypertropia hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia influenza kidney disease lipoatrophic diabetes mellitus lipodystrophy liver cirrhosis lung benign neoplasm lung cancer lung carcinoma mechanical strabismus monocular esotropia nephritis nephrosis obsolete constipation obsolete inherited blood coagulation disease obsolete type 1 diabetes mellitus 9 ophthalmoplegia osteoporosis osteosarcoma peptic esophagitis periodontitis prediabetes syndrome prostate cancer prostate carcinoma pyoureter retinal disease retinitis sleeping sickness specific phobia speech disorder steatotic liver disease strabismus trypanosomiasis 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 vascular disease viral infectious disease visual epilepsy yellow fever
549418	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, gene 2	b4galt1.2	Xenopus tropicalis (tropical clawed frog)	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
768123	DP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, like	b4galt1l	Danio rerio (zebrafish)	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
100145518	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, gene 1	b4galt1.1	Xenopus tropicalis (tropical clawed frog)	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
550425	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	b4galt1	Danio rerio (zebrafish)	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
14595	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	B4galt1	Mus musculus (house mouse)	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
190668	Beta-1,4-N-acetylgalactosaminyltransferase bre-4	bre-4	Caenorhabditis elegans	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease multiple sclerosis
36585	beta1,4-N-acetylgalactosaminyltransferase A	beta4GalNAcTA	Drosophila melanogaster (fruit fly)	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease multiple sclerosis
79586	chondroitin polymerizing factor	CHPF Aliases: CHSY2 CSS2 chondroitin sulfate synthase 2	Homo sapiens (human)	IgA glomerulonephritis cancer central nervous system cancer depressive disorder dysthymic disorder embryoma gliosarcoma high grade glioma major depressive disorder melancholic depression mixed glioma neurotic disorder obsolete melancholia
161198	C-type lectin domain containing 14A	CLEC14A	Homo sapiens (human)	IgA glomerulonephritis breast cancer cancer embryoma lung adenocarcinoma lung cancer melanoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma skin melanoma thymic carcinoma thymoma
10610	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	ST6GALNAC2 Aliases: ST6GalNAII STHM	Homo sapiens (human)	IgA glomerulonephritis breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma depressive disorder embryoma large intestine cancer major depressive disorder melancholic depression melanoma obsolete melancholia skin melanoma thyroid gland follicular carcinoma
98	acylphosphatase 2	ACYP2	Homo sapiens (human)	IgA glomerulonephritis bone osteosarcoma breast cancer bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma embryoma gastrointestinal system cancer gliosarcoma hepatocellular carcinoma high grade glioma kidney cancer large intestine cancer laryngeal squamous cell carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma microphthalmia mixed glioma obsolete Matthew-Wood syndrome osteomyelitis osteosarcoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma
7096	toll like receptor 1	TLR1	Homo sapiens (human)	IgA glomerulonephritis aspergillosis asthma leprosy perinatal necrotizing enterocolitis pulmonary tuberculosis pyelonephritis tuberculosis
21897	toll-like receptor 1	Tlr1	Mus musculus (house mouse)	IgA glomerulonephritis aspergillosis asthma collagen disease glucose metabolism disease leprosy perinatal necrotizing enterocolitis primary immunodeficiency disease pulmonary tuberculosis pyelonephritis tuberculosis
3703	STT3 oligosaccharyltransferase complex catalytic subunit A	STT3A Aliases: MGC9042 STT3-A TMC dolichyl-diphosphooligosaccharide protein glycotransferase	Homo sapiens (human)	IgA glomerulonephritis anthrax disease attention deficit hyperactivity disorder bipolar disorder cervical adenocarcinoma cervical cancer cervix carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital disorder of glycosylation Iw congenital disorder of glycosylation type I congenital disorder of glycosylation depressive disorder epidermodysplasia verruciformis focal epilepsy herpes simplex large intestine cancer major depressive disorder melancholic depression microcephaly mucoepidermoid carcinoma obsolete melancholia partial motor epilepsy schizophrenia skin benign neoplasm skin cancer skin squamous cell carcinoma sleeping sickness thyroid gland follicular carcinoma trypanosomiasis visual epilepsy
3998	lectin, mannose binding 1	LMAN1 Aliases: ERGIC-53 ERGIC53 FMFD1 MCFD1 MR60 endoplasmic reticulum-golgi intermediate compartment protein 53 gp58	Homo sapiens (human)	IgA glomerulonephritis adenocarcinoma adenoma allergic disease arteriosclerotic cardiovascular disease atherosclerosis blood coagulation disease cancer carcinoma colorectal cancer congenital afibrinogenemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia coronary artery disease factor V deficiency factor VII deficiency factor VIII deficiency factor XIII deficiency follicular adenoma hematopoietic system disease large intestine cancer malaria microcystic adenoma nutmeg liver obsolete inherited blood coagulation disease papillary adenoma sarcomatoid carcinoma thanatophoric dysplasia vitamin K deficiency bleeding
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

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