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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 **391826 - 391850** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
53618	fucosyltransferase 8	Fut8	Mus musculus (house mouse)	pulmonary emphysema
53601	protocadherin 12	Pcdh12	Mus musculus (house mouse)
53584	UDP-glycosyltransferase family 37 member B1	Ugt37B1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome bilirubin metabolic disorder hyperthyroidism type 1 diabetes mellitus type 2 diabetes mellitus
53583	UDP-glycosyltransferase family 37 member C1	Ugt37C1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
53550	lectin-24Db	lectin-24Db	Drosophila melanogaster (fruit fly)
53513	UDP-glycosyltransferase family 37 member C2	Ugt37C2	Drosophila melanogaster (fruit fly)	type 2 diabetes mellitus
53512	UDP-glycosyltransferase family 37 member E1	Ugt37E1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
53511	UDP-glycosyltransferase family 37 member D1	Ugt37D1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
53507	UDP-glycosyltransferase family 35 member C1	Ugt35C1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
53506	UDP-glycosyltransferase family 35 member E2	Ugt35E2	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
53504	UDP-glycosyltransferase family 35 member E1	Ugt35E1	Drosophila melanogaster (fruit fly)	hepatitis B type 2 diabetes mellitus
53503	UDP-glycosyltransferase family 303 member A1	Ugt303A1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
53502	UDP-glycosyltransferase family 302 member K1	Ugt302K1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
53501	UDP-glycosyltransferase family 304 member A1	Ugt304A1	Drosophila melanogaster (fruit fly)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
53418	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	B4galt2	Mus musculus (house mouse)
53412	protein phosphatase 1, regulatory subunit 3C	Ppp1r3c	Mus musculus (house mouse)	alcohol use disorder type 2 diabetes mellitus
53374	carbohydrate sulfotransferase 3	Chst3	Mus musculus (house mouse)	osteochondrodysplasia schizophrenia spondyloepiphyseal dysplasia with congenital joint dislocations
52331	starch binding domain 1	Stbd1	Mus musculus (house mouse)
51809	polypeptide N-acetylgalactosaminyltransferase 7	GALNT7 Aliases: GALNAC-T7 polypeptide GalNAc transferase 7	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma colorectal cancer colorectal carcinoma coronary artery disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma gliosarcoma high grade glioma large intestine cancer laryngeal squamous cell carcinoma mixed glioma nasopharynx carcinoma
51805	coenzyme Q3, methyltransferase	COQ3	Homo sapiens (human)
51763	inositol polyphosphate-5-phosphatase K	INPP5K Aliases: SKIP skeletal muscle and kidney enriched inositol phosphatase	Homo sapiens (human)	Aicardi-Goutieres syndrome 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 Duchenne muscular dystrophy Gaucher's disease Laron syndrome Legg-Calve-Perthes disease Marinesco-Sjogren syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia agnosia anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bladder carcinoma breast cancer breast carcinoma cancer cardiovascular system disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cerebral degeneration cerebrovascular disease congenital muscular dystrophy with cataracts and intellectual disability congenital muscular dystrophy congenital nystagmus coronary artery disease dementia depressive disorder developmental coordination disorder disease of mental health disease of metabolism dissociated nystagmus distal myopathy dysplastic nevus syndrome dysthymic disorder dystonia epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis fragile X syndrome generalized anxiety disorder giant cell glioblastoma glioblastoma heart disease hepatocellular carcinoma high grade glioma hypertropia hypogonadism intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia liver cancer major depressive disorder mechanical strabismus melancholic depression melanoma microcephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy neuropathy neurotic disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia oculocerebrorenal syndrome oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pathologic nystagmus peripheral nervous system disease phobic disorder phototoxic dermatitis primary cerebellar degeneration psychotic disorder rippling muscle disease 2 scoliosis skin benign neoplasm skin cancer skin carcinoma skin melanoma spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus tauopathy urinary bladder cancer
51738	ghrelin and obestatin prepropeptide	GHRL	Homo sapiens (human)	Prader-Willi syndrome cardiovascular system disease diabetic neuropathy end stage renal disease esophagus adenocarcinoma middle cerebral artery infarction morbid obesity multiple endocrine neoplasia obesity obstructive sleep apnea type 2 diabetes mellitus
51706	cytochrome b5 reductase 1	CYB5R1 Aliases: humb5R2	Homo sapiens (human)	cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma large intestine cancer
51703	acyl-CoA synthetase long chain family member 5	ACSL5 Aliases: ACS2 ACS5 FACL5 for fatty acid coenzyme A ligase 5 fatty-acid-Coenzyme A ligase, long-chain 5 long-chain acyl-CoA synthetase 5 long-chain fatty acid coenzyme A ligase 5	Homo sapiens (human)	acute chest syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma anaplastic astrocytoma basal cell carcinoma breast cancer breast carcinoma cancer carcinoma celiac disease central nervous system cancer childhood cerebral astrocytoma colorectal cancer colorectal carcinoma congenital diarrhea congestive heart failure coronary thrombosis cribriform carcinoma embryoma endometrial carcinoma essential thrombocythemia familial hyperlipidemia fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer high grade glioma juvenile pilocytic astrocytoma large intestine cancer lung benign neoplasm lung carcinoma malignant astrocytoma migraine mixed glioma myelodysplastic syndrome myocardial infarction obesity pilocytic astrocytoma protoplasmic astrocytoma sarcomatoid carcinoma sebaceous carcinoma silent myocardial infarction steatotic liver disease subependymal giant cell astrocytoma sweat gland cancer systemic lupus erythematosus tubular adenocarcinoma
51700	cytochrome b5 reductase 2	CYB5R2	Homo sapiens (human)	cancer giant cell glioblastoma glioblastoma nasopharynx carcinoma prostate cancer prostate carcinoma

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