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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 **8076 - 8100** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
142680	solute carrier family 34 member 3	SLC34A3	Homo sapiens (human)
10559	solute carrier family 35 member A1	SLC35A1 Aliases: CMP-Sia-Tr CMP-sialic acid transporter CMPST hCST	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 Behcet's disease Marfan syndrome Papillon-Lefevre disease Pick's disease Reye syndrome acute myocardial infarction agranulocytosis amyotrophic lateral sclerosis anhidrosis anterior horn cell disease aortic valve insufficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain disease brain stem infarction cancer cardiovascular system disease cellulitis central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cone-rod dystrophy 2 cone-rod dystrophy congenital disorder of glycosylation Iq congenital disorder of glycosylation type II congenital disorder of glycosylation type IIf congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis diabetic macular edema dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma glucose intolerance heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intellectual disability lateral sclerosis learning disability lingual-facial-buccal dyskinesia liver cancer microcephaly mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 neutropenia obesity obsolete type 1 diabetes mellitus 9 osteoarthritis pathologic nystagmus placental insufficiency pneumonia prediabetes syndrome progressive bulbar palsy progressive muscular atrophy proteinuria severe congenital neutropenia silent myocardial infarction situs inversus spontaneous ocular nystagmus substance abuse substance-related disorder thrombocytopenia tuberous sclerosis 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 ulcerative colitis viral infectious disease visual epilepsy
7355	solute carrier family 35 member A2	SLC35A2 Aliases: UDP-Gal-Tr UDP-galactose translocator UGAT UGT UGT1 UGT2 UGTL	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 Barrett's esophagus Crigler-Najjar syndrome Dandy-Walker syndrome Gilbert syndrome Laron syndrome Pick's disease Reye syndrome West syndrome abdominal obesity-metabolic syndrome 1 achondroplasia adult lymphoma agranulocytosis alternating exotropia anisometropia aromatase excess syndrome autosomal recessive chronic granulomatous disease 1 bacterial infectious disease beta thalassemia bilirubin metabolic disorder bladder carcinoma brain disease breast cancer breast carcinoma cancer carcinoma central nervous system lymphoma central sleep apnea cerebral degeneration childhood lymphoma cholecystolithiasis choledocholithiasis cholelithiasis chronic granulomatous disease clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIm congenital disorder of glycosylation congenital nystagmus craniosynostosis cryptococcosis cyclic hematopoiesis cystinuria developmental and epileptic encephalopathy 36 diarrhea dissociated nystagmus embryoma epilepsy esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esotropia exotropia galactosemia gallbladder disease gastroesophageal reflux disease glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatitis B hepatitis C hepatitis D hyperopia hypertropia hypoglycemia intellectual disability large intestine cancer learning disability leukopenia liver disease lymphoma macular corneal dystrophy mechanical strabismus microcephaly monocular esotropia monocular exotropia neonatal jaundice neutropenia obsolete constipation obsolete infantile epileptic encephalopathy obsolete ymphosarcoma obstructive sleep apnea ophthalmoplegia ovarian cancer ovarian carcinoma pathologic nystagmus peptic esophagitis placental insufficiency primary cutaneous amyloidosis prostate cancer prostate carcinoma pyloric stenosis sarcomatoid carcinoma scoliosis sensorineural hearing loss severe congenital neutropenia sickle cell anemia spontaneous ocular nystagmus steatotic liver disease strabismus syndromic X-linked intellectual disability 94 tetralogy of Fallot thalassemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
23443	solute carrier family 35 member A3	SLC35A3 Aliases: UDP-N-acetylglucosamine transporter	Homo sapiens (human)	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
113829	solute carrier family 35 member A4	SLC35A4	Homo sapiens (human)	breast cancer cancer hepatocellular carcinoma liver cancer lung adenocarcinoma lung cancer multiple myeloma
55032	solute carrier family 35 member A5	SLC35A5 Aliases: FLJ20730	Homo sapiens (human)
10237	solute carrier family 35 member B1	SLC35B1 Aliases: ATP/ADP exchanger in the ER membrane AXER UGTREL1	Homo sapiens (human)
347734	solute carrier family 35 member B2	SLC35B2 Aliases: UGTrel4	Homo sapiens (human)	B-cell lymphoma Hodgkin's granuloma Hodgkin's lymphoma, mixed cellularity Langerhans cell sarcoma Langerhans-cell histiocytosis Richter's syndrome adult lymphoma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer central nervous system lymphoma childhood lymphoma chronic lymphocytic leukemia/small lymphocytic lymphoma chronic lymphocytic leukemia dendritic cell sarcoma dilated cardiomyopathy 1A dilated cardiomyopathy follicular dendritic cell sarcoma follicular lymphoma hereditary multiple exostoses hypomyelinating leukodystrophy 26 interdigitating dendritic cell sarcoma invasive ductal carcinoma lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia mantle cell lymphoma non-Hodgkin lymphoma obesity obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma reticulosarcoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood
51000	solute carrier family 35 member B3	SLC35B3 Aliases: 3' phosphoadenosine 5' phosphosulfate transporter 2 CGI-19 PAPST2 dJ453H5.1	Homo sapiens (human)	diabetes mellitus type 2 diabetes mellitus
84912	solute carrier family 35 member B4	SLC35B4 Aliases: FLJ14697 YEA4	Homo sapiens (human)	prostate cancer prostate carcinoma stomach cancer stomach carcinoma
55343	solute carrier family 35 member C1	SLC35C1 Aliases: FLJ11320 FUCT1 GDP-fucose transporter 1	Homo sapiens (human)	Laron syndrome achondroplasia anxiety disorder cellulitis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc echolalia generalized anxiety disorder hepatocellular carcinoma leukocyte adhesion deficiency 2 leukocyte adhesion deficiency liver cancer microcephaly
51006	solute carrier family 35 member C2	SLC35C2 Aliases: CGI-15 bA394O2.1	Homo sapiens (human)
23169	solute carrier family 35 member D1	SLC35D1 Aliases: KIAA0260 UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter UGTREL7	Homo sapiens (human)	cleft palate cryptorchidism dermatitis elephantiasis fibrochondrogenesis isolated cleft palate lymphedema mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia polyhydramnios schneckenbecken dysplasia
11046	solute carrier family 35 member D2	SLC35D2 Aliases: SQV7L UGTrel8	Homo sapiens (human)
340146	solute carrier family 35 member D3	SLC35D3	Homo sapiens (human)	Hantavirus hemorrhagic fever with renal syndrome Hermansky-Pudlak syndrome abdominal obesity-metabolic syndrome 1 obesity
728661	solute carrier family 35 member E2B	SLC35E2B	Homo sapiens (human)
55508	solute carrier family 35 member E3	SLC35E3 Aliases: BLOV1	Homo sapiens (human)	cardiovascular system disease heart disease
339665	solute carrier family 35 member E4	SLC35E4	Homo sapiens (human)
222553	solute carrier family 35 member F1	SLC35F1 Aliases: dJ230I3.1	Homo sapiens (human)	atrial fibrillation epilepsy giant cell glioblastoma glioblastoma high grade glioma
148641	solute carrier family 35 member F3	SLC35F3 Aliases: FLJ37712	Homo sapiens (human)	acute myeloid leukemia beriberi chronic obstructive pulmonary disease dry beriberi essential hypertension hypertension intracranial aneurysm pellagra thiamine deficiency disease
341880	solute carrier family 35 member F4	SLC35F4 Aliases: FLJ37712	Homo sapiens (human)	acquired immunodeficiency syndrome bipolar disorder
80255	solute carrier family 35 member F5	SLC35F5 Aliases: FLJ22004	Homo sapiens (human)	Kawasaki disease cancer
54978	solute carrier family 35 member F6	SLC35F6 Aliases: ANT2-binding protein ANT2BP FLJ20555 TANGO9 transport and golgi organization 9 homolog (Drosophila)	Homo sapiens (human)	microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma
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
80723	solute carrier family 35 member G2	SLC35G2 Aliases: DKFZp564K2464 MGC3295	Homo sapiens (human)	chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma

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