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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 **6526 - 6550** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
285527	FRY like transcription coactivator	FRYL	Homo sapiens (human)
22877	MLX interacting protein	MLXIP	Homo sapiens (human)
153642	arylsulfatase family member K	ARSK Aliases: DKFZp313G1735 TSULF	Homo sapiens (human)	lysosomal storage disease mucopolysaccharidosis
152831	klotho beta	KLB Aliases: b-Klotho	Homo sapiens (human)	Clostridium difficile colitis allergic rhinitis autosomal dominant hypophosphatemic rickets breast cancer breast carcinoma cancer cartilage-hair hypoplasia diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism embryoma familial hyperlipidemia gestational diabetes hepatocellular carcinoma intrahepatic cholestasis of pregnancy invasive ductal carcinoma irritable bowel syndrome kidney disease kidney failure liver cancer lung cancer lung non-small cell carcinoma neurocirculatory asthenia nodular prostate obesity ovarian disease papillary adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma prostatic adenoma steatotic liver disease thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma type 2 diabetes mellitus uremia vasomotor rhinitis
158234	tRNA methyltransferase 10B	TRMT10B	Homo sapiens (human)
22871	neuroligin 1	NLGN1	Homo sapiens (human)
81610	family with sequence similarity 83 member D	FAM83D	Homo sapiens (human)
57222	endoplasmic reticulum-golgi intermediate compartment 1	ERGIC1	Homo sapiens (human)
56992	kinesin family member 15	KIF15	Homo sapiens (human)
150084	immunoglobulin superfamily member 5	IGSF5	Homo sapiens (human)
1291	collagen type VI alpha 1 chain	COL6A1	Homo sapiens (human)	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
2331	fibromodulin	FMOD Aliases: SLRR2E fibromodulin proteoglycan	Homo sapiens (human)	B-cell lymphoma Richter's syndrome adult cystic teratoma adult lymphoma adult teratoma age related macular degeneration arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast cancer breast carcinoma cancer central nervous system cancer central nervous system lymphoma childhood leukemia childhood lymphoma chronic lymphocytic leukemia colon carcinoma colorectal cancer congestive heart failure coronary artery disease cystic teratoma degeneration of macula and posterior pole embryoma enthesopathy exostosis female stress incontinence fibromyalgia giant cell glioblastoma gingivitis glioblastoma gliosarcoma glomerulonephritis high grade glioma kidney disease leiomyoma leukemia liver cirrhosis lung small cell carcinoma lymphoma macular degeneration malignant teratoma mantle cell lymphoma mature teratoma mixed glioma myofibroma myopia neovascular inflammatory vitreoretinopathy nephritis nephrosis obsolete ymphosarcoma osteoarthritis periarthritis periodontitis prostate cancer prostate carcinoma prostate disease pyoureter tendinitis teratoma uterine fibroid
57333	reticulocalbin 3	RCN3	Homo sapiens (human)
4640	myosin IA	MYO1A	Homo sapiens (human)
53630	beta-carotene oxygenase 1	BCO1	Homo sapiens (human)
27127	structural maintenance of chromosomes 1B	SMC1B	Homo sapiens (human)
9753	zinc finger and SCAN domain containing 12	ZSCAN12	Homo sapiens (human)
219464	olfactory receptor family 5 subfamily T member 2	OR5T2	Homo sapiens (human)
79581	solute carrier family 52 member 2	SLC52A2	Homo sapiens (human)
2571	glutamate decarboxylase 1	GAD1	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 Down syndrome Graves' disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Raynaud disease Reye syndrome Stiff-Person syndrome Sveinsson chorioretinal atrophy Wernicke-Korsakoff syndrome acquired immunodeficiency syndrome acute lymphoblastic leukemia adamantinous craniopharyngioma adult acute lymphocytic leukemia adult respiratory distress syndrome agoraphobia alcohol dependence alcohol use disorder alternating hemiplegia of childhood amnestic disorder amphetamine abuse androgen insensitivity syndrome anthracosilicosis antisocial personality disorder anxiety disorder arteriosclerotic cardiovascular disease asbestosis atherosclerosis atrophic gastritis attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autonomic neuropathy basal ganglia disease bipolar disorder borderline personality disorder bronchus cancer bronchus carcinoma cancer cardiovascular system disease celiac disease central nervous system cancer central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration cerebral palsy childhood acute lymphocytic leukemia chromophobe renal cell carcinoma chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma cleft lip cleft palate cocaine abuse cocaine dependence collecting duct carcinoma colorectal cancer complex partial epilepsy congenital nystagmus congestive heart failure coronary artery disease craniopharyngioma delusional disorder depressive disorder developmental and epileptic encephalopathy 89 diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of mental health dissociated nystagmus dissociative amnesia drug psychosis dysthymic disorder dystonia embryoma encephalitis encephalomyelitis endocrine system disease epilepsy focal epilepsy focal hand dystonia gastric adenocarcinoma generalized anxiety disorder generalized dystonia gestational diabetes gliosarcoma glomerulonephritis glucose intolerance glutaric acidemia I goiter heart disease hemiplegia hemophilia B heroin dependence herpes simplex high grade glioma human immunodeficiency virus infectious disease hyperglycemia hyperlysinemia hyperprolactinemia hyperthyroidism hypochondriasis immune system disease influenza insulinoma intellectual disability intermittent explosive disorder isolated cleft palate kidney disease learning disability lingual-facial-buccal dyskinesia locked-in syndrome lung adenocarcinoma lung cancer lung carcinoma major depressive disorder maturity-onset diabetes of the young melancholic depression microcephaly microphthalmia middle cerebral artery infarction migraine mixed glioma mood disorder morphine dependence multiple sclerosis myelitis nephritis nephrosis nervous system disease neuroblastoma neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neuropathy neurotic disorder newborn respiratory distress syndrome nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete constipation obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea opiate dependence pancreatic cancer pancreatic carcinoma panic disorder papillary craniopharyngioma papillary renal cell carcinoma partial motor epilepsy pathologic nystagmus periodontitis peripheral nervous system disease personality disorder phobic disorder pityriasis rubra pilaris pneumoconiosis pneumocystosis polyneuropathy post-traumatic stress disorder prediabetes syndrome primary cerebellar degeneration progressive multifocal leukoencephalopathy prostate adenocarcinoma prostate cancer prostate carcinoma psychotic disorder pyoureter quadriplegia renal carcinoma renal cell carcinoma retrograde amnesia sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scoliosis seasonal affective disorder sickle cell anemia siderosis social phobia spastic cerebral palsy spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus stereotypic movement disorder substance abuse substance-related disorder temporal lobe epilepsy thyroid gland disease thyrotoxicosis transient cerebral ischemia 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 visual epilepsy withdrawal disorder
2956	mutS homolog 6	MSH6	Homo sapiens (human)
339834	interactor of HORMAD1 1	IHO1	Homo sapiens (human)
23354	HAUS augmin like complex subunit 5	HAUS5	Homo sapiens (human)
10180	RNA binding motif protein 6	RBM6	Homo sapiens (human)
5214	phosphofructokinase, platelet	PFKP Aliases: PFK-C PFKF Phosphofructokinase, platelet type	Homo sapiens (human)	adenocarcinoma adenoma breast cancer cancer cholangiocarcinoma cribriform carcinoma disease of metabolism embryoma glycogen storage disease granular cell carcinoma intrahepatic cholangiocarcinoma obesity pancreatic cancer pancreatic carcinoma renal tubular acidosis tubular adenocarcinoma

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