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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 **1001 - 1025** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
64409	polypeptide N-acetylgalactosaminyltransferase 17	GALNT17 Aliases: GALNTL3 GalNAc-T17 GalNAc-T19 GalNAc-T5L polypeptide GalNAc transferase 3 polypeptide N-acetylgalactosaminyltransferase-like 3 ppGalNAc-T17	Homo sapiens (human)	allergic asthma asthma autism spectrum disorder autistic disorder intrinsic asthma
57452	polypeptide N-acetylgalactosaminyltransferase 16	GALNT16 Aliases: GalNAc-T16 KIAA1130 polypeptide GalNAc transferase 16	Homo sapiens (human)	breast cancer breast carcinoma idiopathic scoliosis
117248	polypeptide N-acetylgalactosaminyltransferase 15	GALNT15 Aliases: GALNT7 polypeptide GalNAc transferase 15 pp-GalNAc-T15	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
79623	polypeptide N-acetylgalactosaminyltransferase 14	GALNT14 Aliases: FLJ12691 GalNac-T10 GalNac-T14 polypeptide GalNAc transferase 14	Homo sapiens (human)	Balo concentric sclerosis Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia adrenoleukodystrophy autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal cell carcinoma breast cancer breast carcinoma cancer central nervous system disease chondrodysplasia-pseudohermaphroditism syndrome colorectal cancer colorectal carcinoma corneal disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma keratoconus large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II narcolepsy neuroblastoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma signet ring cell adenocarcinoma skin melanoma
114805	polypeptide N-acetylgalactosaminyltransferase 13	GALNT13 Aliases: GalNAc-T13 KIAA1918 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 13 polypeptide GalNAc transferase 13	Homo sapiens (human)	cancer chronic obstructive pulmonary disease lung benign neoplasm lung carcinoma sickle cell anemia
79695	polypeptide N-acetylgalactosaminyltransferase 12	GALNT12 Aliases: GalNAc-T12 polypeptide GalNAc transferase 12	Homo sapiens (human)	adenocarcinoma adenoma bilateral breast cancer cancer colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma islet cell tumor large intestine cancer microcystic adenoma papillary adenoma
63917	polypeptide N-acetylgalactosaminyltransferase 11	GALNT11 Aliases: GalNAc-T11 polypeptide GalNAc transferase 11	Homo sapiens (human)	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
55568	polypeptide N-acetylgalactosaminyltransferase 10	GALNT10 Aliases: GalNAc-T10 polypeptide GalNAc transferase 10	Homo sapiens (human)	hepatitis B hepatocellular carcinoma liver cancer schizophrenia
2589	polypeptide N-acetylgalactosaminyltransferase 1	GALNT1 Aliases: GalNAc-T1 polypeptide GalNAc transferase 1 protein-UDP acetylgalactosaminyltransferase 1	Homo sapiens (human)	colorectal cancer colorectal carcinoma congenital heart disease congestive heart failure heart valve disease hepatocellular carcinoma large intestine cancer liver cancer ovarian cancer ovarian carcinoma pulmonary valve stenosis stomach cancer stomach carcinoma
2588	galactosamine (N-acetyl)-6-sulfatase	GALNS Aliases: GALNAC6S GAS GalN6S Morquio syndrome N-acetylgalactosamine-6-sulfatase chondroitinase chondroitinsulfatase galactose-6-sulfate sulfatase mucopolysaccharidosis type IVA	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 GM1 gangliosidosis Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Wilson disease achondroplasia acne adenine phosphoribosyltransferase deficiency adenocarcinoma adenoma age related macular degeneration amyloidosis anthrax disease anxiety disorder arachnoiditis bacterial meningitis bacterial sepsis bacterial vaginosis bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease cerebral degeneration cholangiocarcinoma chronic lymphocytic leukemia chronic obstructive pulmonary disease chronic ulcer of skin colorectal cancer colorectal carcinoma cribriform carcinoma degeneration of macula and posterior pole dental caries dentin caries diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism embryoma enterocele generalized anxiety disorder glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemochromatosis hole retinal cyst impetigo influenza inguinal hernia intrahepatic cholangiocarcinoma iron metabolism disease kidney disease large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease macular degeneration macular holes mastitis meningitis metachromatic leukodystrophy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia myositis necrotizing fasciitis nephritis osteochondrodysplasia osteoporosis pharyngitis phobic disorder prostate cancer prostate carcinoma psychotic disorder pyoderma retinal perforation rheumatic fever scarlet fever scoliosis sensorineural hearing loss stomach cancer stomach carcinoma tonsillitis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus vaginitis viral meningitis vulvitis vulvovaginitis
130589	galactose mutarotase	GALM Aliases: aldose 1-epimerase aldose mutarotase galactomutarotase	Homo sapiens (human)	Crohn's colitis Crohn's disease classic galactosemia colitis colorectal cancer colorectal carcinoma galactokinase deficiency galactosemia gastroenteritis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease 2 inflammatory bowel disease large intestine cancer ulcerative colitis
2585	galactokinase 2	GALK2 Aliases: GK2	Homo sapiens (human)	bronchus cancer bronchus carcinoma dental caries dentin caries lung adenocarcinoma lung cancer lung carcinoma
2584	galactokinase 1	GALK1	Homo sapiens (human)	cancer 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 classic galactosemia colorectal cancer colorectal carcinoma cutaneous fibrous histiocytoma cystinuria diabetic cataract disease of metabolism epidermolysis bullosa simplex localized type epidermolysis bullosa simplex galactokinase deficiency galactose epimerase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma hidradenoma inherited metabolic disorder junctional epidermolysis bullosa non-Herlitz type junctional epidermolysis bullosa with pyloric atresia junctional epidermolysis bullosa large intestine cancer liver cancer placental insufficiency senile cataract skin papilloma skin tag syringoma
2582	UDP-galactose-4-epimerase	GALE Aliases: SDR1E1 UDP-glucose 4-epimerase short chain dehydrogenase/reductase family 1E, member 1	Homo sapiens (human)	Guillain-Barre syndrome Miller Fisher syndrome benign familial infantile epilepsy benign familial neonatal epilepsy benign neonatal seizures classic galactosemia cystinuria galactokinase deficiency galactose epimerase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease stomach cancer stomach carcinoma thrombocytopenia tuberculosis
2581	galactosylceramidase	GALC Aliases: Krabbe disease	Homo sapiens (human)	Creutzfeldt-Jakob disease Evans' syndrome Fabry disease Farber lipogranulomatosis Gaucher's disease Krabbe disease Mycoplasma pneumoniae pneumonia Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wolman disease amblyopia autoimmune thrombocytopenic purpura bipolar disorder blindness bronchus cancer bronchus carcinoma cancer cerebellar ataxia cerebellar disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital nystagmus demyelinating disease depressive disorder disease of metabolism dissociated nystagmus dysthymic disorder embryoma epilepsy glycogen storage disease II head and neck cancer head and neck squamous cell carcinoma hydrocephalus hypertropia inflammatory bowel disease laryngeal disease late onset Parkinson's disease leukodystrophy lipid storage disease low tension glaucoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease major depressive disorder mechanical strabismus melancholic depression melanoma metachromatic leukodystrophy multiple sclerosis nasopharynx carcinoma neurodegenerative disease neurotic disorder obsolete melancholia obstructive hydrocephalus ophthalmoplegia optic atrophy osteomalacia paraplegia pathologic nystagmus placental insufficiency primary open angle glaucoma relapsing fever rickets schizophrenia senile degeneration of brain sensorineural hearing loss sphingolipidosis spontaneous ocular nystagmus squamous cell carcinoma status epilepticus strabismic amblyopia strabismus systemic lupus erythematosus tongue squamous cell carcinoma tracheal disease visual epilepsy
79690	galactose-3-O-sulfotransferase 4	GAL3ST4 Aliases: FLJ12116	Homo sapiens (human)	leprosy
89792	galactose-3-O-sulfotransferase 3	GAL3ST3 Aliases: GAL3ST2	Homo sapiens (human)
64090	galactose-3-O-sulfotransferase 2	GAL3ST2 Aliases: GP3ST	Homo sapiens (human)	Crohn's colitis Crohn's disease ankylosing spondylitis ascending cholangitis cholangitis inflammatory bowel disease 1 inflammatory bowel disease parapsoriasis primary sclerosing cholangitis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole sclerosing cholangitis suppurative cholangitis ulcerative colitis
9514	galactose-3-O-sulfotransferase 1	GAL3ST1 Aliases: CST cerebroside (3' phosphoadenylylsulfate:galactosylceramide 3') sulfotransferase	Homo sapiens (human)	Behcet's disease Marfan syndrome Papillon-Lefevre disease acute myocardial infarction adenocarcinoma adenoma amyotrophic lateral sclerosis anhidrosis anterior horn cell disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain stem infarction breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy 2 cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis diabetic macular edema embryoma episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma granular cell carcinoma heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza invasive ductal carcinoma lateral sclerosis liver cancer mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 osteoarthritis papillary renal cell carcinoma progressive bulbar palsy progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction situs inversus stomach cancer stomach carcinoma substance abuse substance-related disorder tuberous sclerosis tubular adenocarcinoma 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
2572	glutamate decarboxylase 2	GAD2 Aliases: GAD65	Homo sapiens (human)	Addison's disease 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 Balo concentric sclerosis Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Miller-Dieker lissencephaly syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Smith-Magenis syndrome Stiff-Person syndrome West Nile fever adrenal cortical hypofunction adrenoleukodystrophy agnosia alcohol dependence alcohol use disorder alternating hemiplegia of childhood amnestic disorder amphetamine abuse anxiety disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autonomic neuropathy basal ganglia disease bipolar disorder borderline personality disorder breast cancer breast carcinoma cancer cardiac arrest celiac disease central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration cocaine abuse cocaine dependence colorectal cancer colorectal carcinoma complex partial epilepsy craniosynostosis delusional disorder depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of mental health disease of metabolism dissociative amnesia drug psychosis dysthymic disorder embryoma encephalitis encephalomyelitis epilepsy essential hypertension focal epilepsy generalized anxiety disorder gestational diabetes glomerulonephritis glucose intolerance goiter heroin dependence herpes simplex hypertension hyperthyroidism idiopathic generalized epilepsy immune system disease insulinoma intermittent explosive disorder ischiocoxopodopatellar syndrome kidney disease kwashiorkor large intestine cancer major depressive disorder marasmus melancholic depression middle cerebral artery infarction mood disorder morbid obesity morphine dependence multiple sclerosis myelitis myotonic dystrophy type 1 narcolepsy nephritis nephrosis nervous system disease neuromuscular junction 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 neurotic disorder nutrition disease obesity obsessive-compulsive disorder obsolete melancholia obsolete type 1 diabetes mellitus 9 pancreatic cancer pancreatic carcinoma panic disorder partial motor epilepsy pernicious anemia phobic disorder prediabetes syndrome prostate cancer prostate carcinoma protein-energy malnutrition psychotic disorder pyoureter retinal disease retinitis schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease spastic cerebral palsy temporal lobe epilepsy thyroid gland disease thyrotoxicosis transient cerebral ischemia 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
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
2548	alpha glucosidase	GAA Aliases: Pompe disease glycogen storage disease type II	Homo sapiens (human)	Becker muscular dystrophy Clouston syndrome Duchenne muscular dystrophy Fabry disease Friedreich ataxia 1 Friedreich ataxia aortic aneurysm ataxia telangiectasia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect 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 cancer cardiomyopathy cerebellar ataxia cerebellar disease chylomicron retention disease cystinuria cytochrome-c oxidase deficiency disease diaphragm disease disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease membranous glomerulonephritis mitochondrial metabolism disease mitochondrial myopathy muscular dystrophy myopathy neurodegenerative disease neuromuscular disease 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 oculopharyngeal muscular dystrophy patent foramen ovale peroxisome biogenesis disorder 7A primary immunodeficiency disease sensorineural hearing loss thyroid gland anaplastic carcinoma
2539	glucose-6-phosphate dehydrogenase	G6PD Aliases: G6PD1	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 B-cell lymphoma Baraitser-Winter syndrome Bartter disease Bloch-Sulzberger syndrome Burkitt lymphoma Chagas disease Conn's syndrome Creutzfeldt-Jakob disease Duchenne muscular dystrophy Emery-Dreifuss muscular dystrophy Fabry disease Fraser syndrome Gilbert syndrome Goldenhar syndrome IGSF1 deficiency syndrome Japanese encephalitis Langerhans-cell histiocytosis Moebius syndrome Muenke Syndrome Nance-Horan syndrome Native American myopathy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Plasmodium ovale malaria Plasmodium vivax malaria Renpenning syndrome Reye syndrome Richter's syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Waterhouse-Friderichsen syndrome Weissenbacher-Zweymuller syndrome Werner syndrome Wilson disease Wiskott-Aldrich syndrome X-linked chronic granulomatous disease abdominal obesity-metabolic syndrome 1 achromatopsia acoustic neuroma acquired color blindness acquired immunodeficiency syndrome acquired polycythemia acute chest syndrome acute kidney failure acute lymphoblastic leukemia acute megakaryocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal cortex cancer adrenal gland cancer adrenoleukodystrophy adult acute lymphocytic leukemia adult hepatocellular carcinoma adult lymphoma age related macular degeneration allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia amyloidosis anaplastic astrocytoma anemia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anogenital venereal wart asthma ataxia telangiectasia atypical chronic myeloid leukemia, BCR-ABL1 negative atypical hemolytic-uremic syndrome autistic disorder bacterial sepsis beta thalassemia bilirubin metabolic disorder bipolar disorder bladder carcinoma blastomycosis blood group incompatibility blue color blindness bone marrow cancer borderline personality disorder brain cancer brain ischemia brain stem infarction branchiootic syndrome breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiomyopathy cardiovascular system disease cataract central nervous system cancer central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood hepatocellular carcinoma childhood leukemia childhood lymphoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chromophobe renal cell carcinoma chronic granulomatous disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chylomicron retention disease classic galactosemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma common cold common wart conduct disorder cone-rod dystrophy congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia congenital hemolytic anemia congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nonspherocytic hemolytic anemia congestive heart failure contact dermatitis coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma cutaneous leishmaniasis cystinuria degeneration of macula and posterior pole dementia dengue disease dengue hemorrhagic fever diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism duodenum cancer embryoma endocarditis endomyocardial fibrosis epilepsy epithelioid malignant peripheral nerve sheath tumor erythropoietin polycythemia esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia factor VIII deficiency familial adenomatous polyposis 1 familial adenomatous polyposis familial erythrocytosis 2 familial hyperlipidemia familial periodic paralysis favism fetal erythroblastosis fibrillary astrocytoma fragile X syndrome fundus albipunctatus galactokinase deficiency galactosemia gemistocytic astrocytoma gliosarcoma glomerulonephritis glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart cancer heart disease hematologic cancer hematopoietic system disease hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobin H disease hemoglobinopathy hemoglobinuria hemolytic anemia hemolytic-uremic syndrome hemophilia B hepatic coma hepatic encephalopathy hepatitis A hepatitis B hepatitis hepatoblastoma hepatocellular carcinoma hereditary elliptocytosis hereditary spherocytosis hidradenoma high grade glioma human immunodeficiency virus infectious disease hyperhomocysteinemia hyperparathyroidism hypertension hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia hypomelanosis of Ito hypothyroidism inherited metabolic disorder intellectual disability intermittent explosive disorder intrinsic asthma iron metabolism disease juvenile pilocytic astrocytoma kernicterus due to isoimmunization kernicterus kidney cancer kidney disease large intestine cancer learning disability leishmaniasis leukemia lingual-facial-buccal dyskinesia lipid storage disease liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macrocytic anemia macular degeneration malaria malignant astrocytoma malignant peripheral nerve sheath tumor melanoma metabolic dysfunction-associated steatotic liver disease methemoglobinemia middle cerebral artery infarction mixed glioma movement disease mucocutaneous leishmaniasis multiple myeloma muscular dystrophy myelodysplastic syndrome myelofibrosis myeloid leukemia myeloproliferative neoplasm myocardial infarction myopathy myxedema neonatal jaundice nephritis nephrogenic diabetes insipidus nephrosis neurilemmoma neuroblastoma neurodegenerative disease neurofibromatosis 1 neurofibromatosis neurofibrosarcoma non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete subacute myeloid leukemia obsolete ymphosarcoma occupational dermatitis oculocerebrorenal syndrome orofaciodigital syndrome I orofaciodigital syndrome X osteitis fibrosa pancytopenia papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis parathyroid adenoma parathyroid carcinoma paroxysmal nocturnal hemoglobinuria peroxisome biogenesis disorder 8A phagocyte bactericidal dysfunction phenylketonuria pheochromocytoma pilocytic astrocytoma plasmacytoma pneumocystosis polycythemia vera polycythemia prediabetes syndrome priapism primary hyperaldosteronism primary immunodeficiency disease primary pulmonary hypertension progeria prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder pterygium pyoureter pyruvate kinase deficiency of red cells red color blindness red-green color blindness renal carcinoma renal cell carcinoma renovascular hypertension reticulosarcoma retinitis pigmentosa rhabdomyosarcoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder senile cataract sickle cell anemia silent myocardial infarction skin melanoma skin papilloma skin tag small intestine cancer spondylocarpotarsal synostosis syndrome steatotic liver disease stress polycythemia subependymal giant cell astrocytoma sulfhemoglobinemia syringoma thalassemia thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma transient cerebral ischemia trypanosomiasis tubular adenocarcinoma 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 urinary bladder cancer vascular dementia vascular disease vertebrobasilar insufficiency viral infectious disease visceral leishmaniasis visual epilepsy vitiligo yellow fever
92579	glucose-6-phosphatase catalytic subunit 3	G6PC3 Aliases: UGRP	Homo sapiens (human)	Crohn's colitis Crohn's disease Marfan syndrome Wiskott-Aldrich syndrome acute myeloid leukemia agranulocytosis androgen insensitivity syndrome anemia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect bacterial sepsis bronchiectasis cancer cleft palate colitis congenital heart disease cryptorchidism cyclic hematopoiesis cystinuria embryoma essential thrombocythemia eunuchism galactosemia gastroenteritis glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hydronephrosis hypogonadism ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability isolated cleft palate learning disability leukopenia lymphopenia macrocytic anemia microcephaly mitral valve insufficiency mitral valve prolapse myelodysplastic syndrome neutropenia oculocutaneous albinism pancytopenia patent ductus arteriosus patent foramen ovale premature menopause primary immunodeficiency disease primary pulmonary hypertension pulmonary valve stenosis sensorineural hearing loss severe congenital neutropenia 4 severe congenital neutropenia situs inversus thrombocytopenia tuberous sclerosis ulcerative colitis varicose veins
57818	glucose-6-phosphatase catalytic subunit 2	G6PC2 Aliases: IGRP islet specific glucose 6 phosphatase catalytic subunit related protein	Homo sapiens (human)	Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 breast cancer breast carcinoma cystinuria diabetes mellitus diabetic ketoacidosis galactosemia gestational diabetes glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hyperglycemia hyperinsulinism insulinoma obsolete type 1 diabetes mellitus 9 prediabetes 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

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GlyTouCan

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GlycoPOST

UniCarb-DR

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