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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 **1551 - 1575** of **1582** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
401494	3-hydroxyacyl-CoA dehydratase 4	HACD4 Aliases: Em:AL662879.1 OTTHUMG00000021016 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4	Homo sapiens (human)	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer
402635	galectin-related inter-fiber protein	GRIFIN	Homo sapiens (human)
414328	IDNK gluconokinase	IDNK Aliases: bA522I20.2 hGntK	Homo sapiens (human)
440138	ALG11 alpha-1,2-mannosyltransferase	ALG11 Aliases: CDG1P GDP-Man:Man(3)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase KIAA0266	Homo sapiens (human)	cerebral degeneration congenital disorder of glycosylation Ip congenital disorder of glycosylation type I congenital disorder of glycosylation epilepsy hypertropia inherited metabolic disorder intellectual disability learning disability mechanical strabismus microcephaly ophthalmoplegia scoliosis sensorineural hearing loss strabismus visual epilepsy
441531	phosphoglycerate mutase family member 4	PGAM4 Aliases: PGAM-B PGAM1 PGAM3 dJ1000K24.1	Homo sapiens (human)	male infertility
442117	polypeptide N-acetylgalactosaminyltransferase like 6	GALNTL6 Aliases: GALNT17 GalNAc-T6L polypeptide GalNAc transferase-like 6	Homo sapiens (human)	nicotine dependence
493869	glutathione peroxidase 8 (putative)	GPX8 Aliases: EPLA847 UNQ847	Homo sapiens (human)
497190	C-type lectin domain family 18 member B	CLEC18B	Homo sapiens (human)	acquired immunodeficiency syndrome cancer embryoma giant cell glioblastoma glioblastoma high grade glioma
574537	UDP glucuronosyltransferase family 2 member A2	UGT2A2	Homo sapiens (human)	ovarian cancer ovarian carcinoma
606495	cytochrome b5 reductase like	CYB5RL Aliases: LOC606495	Homo sapiens (human)
641371	acyl-CoA thioesterase 1	ACOT1 Aliases: ACH2 CTE-1 LACH2	Homo sapiens (human)	gastric adenocarcinoma hepatocellular carcinoma liver cancer
643664	solute carrier family 35 member G6	SLC35G6	Homo sapiens (human)
644974	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase like 2	ALG1L2	Homo sapiens (human)	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
646000	solute carrier family 35 member G4	SLC35G4	Homo sapiens (human)
648791	protein phosphatase 1 regulatory subunit 3G	PPP1R3G	Homo sapiens (human)	obesity steatotic liver disease
653308	N-acylsphingosine amidohydrolase 2B	ASAH2B Aliases: ASAH2L bA449O16.3 bA98I6.3	Homo sapiens (human)	breast cancer breast carcinoma
653509	surfactant protein A1	SFTPA1 Aliases: COLEC4 SP-A SP-A1 surfactant, pulmonary-associated protein A1A	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 Hermansky-Pudlak syndrome Pick's disease Reye syndrome T cell deficiency X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis amnestic disorder amyloidosis anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial pneumonia bacterial sepsis bronchiectasis bronchiolitis obliterans bronchiolitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types cerebral degeneration cerebral infarction cerebrovascular disease chronic ethmoiditis chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cryptogenic organizing pneumonia cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma esophagitis essential thrombocythemia extrinsic allergic alveolitis familial periodic paralysis gastroesophageal reflux disease granular cell carcinoma heart disease hematologic cancer hydrocephalus hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease interstitial lung disease interstitial nephritis intrinsic asthma keratoconus liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis macrocytic anemia mastitis myelodysplastic syndrome myopathy neurodegenerative disease newborn respiratory distress syndrome obesity obsolete T lymphocyte deficiency obstructive hydrocephalus obstructive lung disease osteomalacia otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis pulmonary alveolar proteinosis pulmonary edema pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory syncytial virus infectious disease retrograde amnesia rickets secondary hypertrophic osteoarthropathy senile degeneration of brain shigellosis sinusitis squamous cell carcinoma staphyloenterotoxemia systolic heart failure tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis viral infectious disease
654346	galectin 9C	LGALS9C	Homo sapiens (human)	cancer
727936	glucoside xylosyltransferase 2	GXYLT2	Homo sapiens (human)
728661	solute carrier family 35 member E2B	SLC35E2B	Homo sapiens (human)
728819	C1GALT1 specific chaperone 1 like	C1GALT1C1L	Homo sapiens (human)
729020	ribulose-5-phosphate-3-epimerase like 1	RPEL1	Homo sapiens (human)
729201	sperm acrosome associated 5B	SPACA5B Aliases: LYZL5B	Homo sapiens (human)
729238	surfactant protein A2	SFTPA2 Aliases: COLEC5 SP-A2 surfactant, pulmonary-associated protein A2A	Homo sapiens (human)	Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis ankylosing spondylitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial pneumonia bacterial sepsis bronchiectasis bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types chronic obstructive pulmonary disease communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cystic fibrosis embryoma esophagitis gastroesophageal reflux disease granular cell carcinoma heart disease hydrocephalus hypereosinophilic syndrome hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease interstitial nephritis intrinsic asthma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis newborn respiratory distress syndrome obesity obstructive hydrocephalus obstructive lung disease otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis pulmonary fibrosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory failure respiratory syncytial virus infectious disease rheumatoid arthritis secondary hypertrophic osteoarthropathy senile degeneration of brain spondyloarthropathy spondylosis squamous cell carcinoma tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis
729920	CDP-L-ribitol pyrophosphorylase A	CRPPA Aliases: 4-diphosphocytidyl-2C-methyl-D-erythritol synthase homolog (Arabidopsis) D-ribitol-5-phosphate cytidylyltransferase IspD Nip hCG_1745121 notch1-induced protein	Homo sapiens (human)	Axenfeld-Rieger syndrome Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia anemia 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 bilateral optic nerve hypoplasia cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy A7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly macrocytic anemia microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myositis nonpapillary renal cell carcinoma 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy papillary renal cell carcinoma persistent hyperplastic primary vitreous pneumonia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion renal carcinoma renal cell carcinoma retinal detachment rippling muscle disease 2 sarcomatoid renal cell carcinoma scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy

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