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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 **126 - 150** of **1582** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
197258	fucose kinase	FCSK Aliases: FLJ39408 L-fucose kinase	Homo sapiens (human)	congenital disorder of glycosylation congenital nystagmus dissociated nystagmus epilepsy esophagitis gastroesophageal reflux disease hypertropia intellectual disability learning disability mechanical strabismus ophthalmoplegia optic atrophy pathologic nystagmus peptic esophagitis spontaneous ocular nystagmus strabismus visual epilepsy
197257	lactate dehydrogenase D	LDHD	Homo sapiens (human)	aniridia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma intellectual disability learning disability microcephaly nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
197021	lactase like	LCTL Aliases: FLJ33279 KL lactase phlorizin hydrolase KLG KLPH gammaklotho klotho gamma	Homo sapiens (human)	arthritis arthropathy kidney disease osteoarthritis
196051	phospholipid phosphatase 4	PLPP4 Aliases: DPPL2 diacylglycerol pyrophosphate phosphatase-like 2	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 breast cancer bronchus cancer bronchus carcinoma cerebral degeneration lung cancer lung carcinoma lung squamous cell carcinoma prostate cancer prostate carcinoma
192134	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	B3GNT6 Aliases: B3Gn-T6 core 3 synthase	Homo sapiens (human)	cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma familial adenomatous polyposis 1 familial adenomatous polyposis islet cell tumor large intestine cancer pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma
171546	serine palmitoyltransferase small subunit A	SPTSSA Aliases: small subunit of serine palmitoyltransferase A ssSPTa	Homo sapiens (human)	hereditary spastic paraplegia 90A hereditary spastic paraplegia 90B
171169	sperm acrosome associated 4	SPACA4 Aliases: SAMP14	Homo sapiens (human)
170384	fucosyltransferase 11	FUT11 Aliases: MGC33202 alpha (1,3) fucosyltransferase	Homo sapiens (human)	bronchus cancer bronchus carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatocellular carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stomach cancer
168391	polypeptide N-acetylgalactosaminyltransferase like 5	GALNTL5 Aliases: GalNAc-T5L polypeptide GalNAc transferase-like 5	Homo sapiens (human)	actinic keratosis gastric adenocarcinoma male infertility seborrheic keratosis skin disease
167127	UDP glycosyltransferase family 3 member A2	UGT3A2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
166929	sphingomyelin synthase 2	SGMS2 Aliases: MGC26963 SMS2	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 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bacterial sepsis bone osteosarcoma breast cancer breast carcinoma calvarial doughnut lesions with bone fragility cancer central nervous system cancer cerebral degeneration colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease dental caries dentin caries depressive disorder dysthymic disorder embryoma gastroenteritis gliosarcoma high grade glioma ileitis ileocolitis large intestine cancer major depressive disorder melancholic depression mixed glioma neurotic disorder obesity obsolete melancholia osteoporosis osteosarcoma pulmonary emphysema scoliosis steatotic liver disease
166012	carbohydrate sulfotransferase 13	CHST13 Aliases: C4ST3 chondroitin 4-sulfotransferase 3	Homo sapiens (human)	arthritis arthropathy osteoarthritis primary pulmonary hypertension
165679	serine palmitoyltransferase small subunit B	SPTSSB Aliases: ADMP androgen down regulated in mouse prostate small subunit of serine palmitoyltransferase B ssSPTb	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease
165631	poly(ADP-ribose) polymerase family member 15	PARP15 Aliases: ARTD7 BAL3 FLJ40597 pART7	Homo sapiens (human)	atherosclerosis cancer depressive disorder embryoma major depressive disorder melancholic depression obsolete melancholia
162466	phosphoethanolamine/phosphocholine phosphatase 1	PHOSPHO1	Homo sapiens (human)	diabetes mellitus osteomalacia rickets type 2 diabetes mellitus
161357	MAM domain containing glycosylphosphatidylinositol anchor 2	MDGA2	Homo sapiens (human)	Balo concentric sclerosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy benign epilepsy with centrotemporal spikes cancer central nervous system disease dissociative disorder embryoma microinvasive gastric cancer narcolepsy neurotic disorder rheumatoid arthritis sexual dysfunction stomach cancer stomach carcinoma systemic lupus erythematosus
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
160851	diacylglycerol kinase eta	DGKH Aliases: DGKeta	Homo sapiens (human)	allergic asthma asthma attention deficit hyperactivity disorder bipolar disorder borderline personality disorder bronchus cancer bronchus carcinoma disease of mental health esophageal cancer esophageal carcinoma intermittent explosive disorder intrinsic asthma lung benign neoplasm lung cancer lung carcinoma melancholic depression mood disorder nephrolithiasis neurotic disorder obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia panic disorder psychotic disorder schizophrenia uric acid nephrolithiasis
160418	transmembrane O-mannosyltransferase targeting cadherins 3	TMTC3 Aliases: FLJ90492 SMILE	Homo sapiens (human)	Joubert syndrome Miller-Dieker lissencephaly syndrome acute myocardial infarction adult lymphoma agranulocytosis aortic aneurysm aortic valve insufficiency blood coagulation disease breast cancer breast carcinoma cancerophobia central nervous system lymphoma childhood lymphoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure coronary thrombosis cortical dysplasia-focal epilepsy syndrome dental caries dentin caries dermoid cyst of ovary dermoid cyst enterocele epilepsy focal epilepsy hydranencephaly hydrocephalus intellectual disability learning disability leukopenia lissencephaly 8 lissencephaly lung cancer lung non-small cell carcinoma lymphoma myocardial infarction myopia neutropenia obsolete malignant histiocytosis obsolete ymphosarcoma optic atrophy partial motor epilepsy periventricular nodular heterotopia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pyloric stenosis septooptic dysplasia severe congenital neutropenia short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction syndromic X-linked intellectual disability Najm type visual epilepsy
160364	C-type lectin domain family 12 member A	CLEC12A Aliases: CD371 CLL-1 DCAL-2 MICL dendritic cell-associated lectin 2 myeloid inhibitory C-type lectin-like receptor	Homo sapiens (human)	Crohn's colitis Crohn's disease Richter's syndrome acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia arthritis arthropathy cancer childhood leukemia chronic fatigue syndrome chronic lymphocytic leukemia chronic myeloid leukemia dermatophytosis embryoma encephalitis encephalomyelitis essential thrombocythemia fungal infectious disease immune system disease inflammatory bowel disease 1 inflammatory bowel disease leukemia lymphoblastic lymphoma lymphocytic choriomeningitis lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma rheumatoid arthritis ulcerative colitis
160335	transmembrane O-mannosyltransferase targeting cadherins 2	TMTC2 Aliases: DKFZp762A217	Homo sapiens (human)	allergic asthma asthma dermatitis glaucoma intrinsic asthma low tension glaucoma mutism primary open angle glaucoma sensorineural hearing loss
160287	lactate dehydrogenase A like 6A	LDHAL6A Aliases: LDH6A MGC23940	Homo sapiens (human)	disease of metabolism
159371	solute carrier family 35 member G1	SLC35G1 Aliases: C10orf60 FLJ33990 POST partner of STIM1	Homo sapiens (human)	Laron syndrome Werner syndrome acute myeloid leukemia agnosia arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis atrial fibrillation autistic disorder breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma coronary artery disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dysthymic disorder embryoma epilepsy hemolytic-uremic syndrome hepatoblastoma hepatocellular carcinoma hyperglycemia intussusception kidney failure large intestine cancer leukemia major depressive disorder melancholic depression mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 neurotic disorder nutmeg liver obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 occipital horn syndrome polycystic ovary syndrome progeria prostate cancer prostate carcinoma schizophrenia sensorineural hearing loss transient myeloproliferative syndrome 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 uremia
158326	FRAS1 related extracellular matrix 1	FREM1 Aliases: C9orf143 C9orf145 DKFZp686M16108 FLJ25461 TILRR	Homo sapiens (human)	3p deletion syndrome Angelman syndrome Baraitser-Winter syndrome CAKUT Fraser syndrome 1 Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome NFIA-related disorder Nance-Horan syndrome Potter's syndrome SATB2-associated syndrome Sakati-Nyhan syndrome Smith-Magenis syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome acquired immunodeficiency syndrome anorectal stricture bilateral renal aplasia branchiootic syndrome cardiovascular system disease chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia craniosynostosis distal 10q deletion syndrome eye disease heart disease hiatus hernia human immunodeficiency virus infectious disease microphthalmia myelofibrosis omphalocele orofaciodigital syndrome I orofaciodigital syndrome X rectal prolapse renal agenesis umbilical hernia
154790	C-type lectin domain family 2 member L	CLEC2L Aliases: FLJ32986	Homo sapiens (human)

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