GlyCosmos Portal

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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 **276 - 300** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
1103	choline O-acetyltransferase	CHAT	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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Balo concentric sclerosis Down syndrome Gilles de la Tourette syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lambert-Eaton myasthenic syndrome Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Rett syndrome Reye syndrome X-linked adrenal hypoplasia congenita acute myocardial infarction adrenoleukodystrophy agnosia allergic asthma amnestic disorder amyloidosis angle-closure glaucoma arthritis arthropathy aspiration pneumonia aspiration pneumonitis asthma atrial fibrillation autism spectrum disorder autistic disorder beriberi bronchus cancer bronchus carcinoma bulbar polio cancer cannabis abuse cannabis dependence central nervous system disease central sleep apnea centronuclear myopathy cerebral degeneration cerebral infarction cerebrovascular disease chronic closed-angle glaucoma chronic fatigue syndrome clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital myasthenic syndrome 21 congenital myasthenic syndrome 6 congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy coronary thrombosis critical illness polyneuropathy dementia depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis differentiating neuroblastoma disease of mental health dissociated nystagmus dry beriberi dysthymic disorder encephalitis encephalomyelitis epilepsy esophagitis esotropia focal epilepsy gastroesophageal reflux disease gastroparesis giant cell glioblastoma glioblastoma hypertropia hypoglycemia idiopathic interstitial pneumonia intellectual disability intrinsic asthma kernicterus due to isoimmunization kernicterus lactic acidosis large intestine cancer learning disability lung benign neoplasm lung cancer lung carcinoma lymphocytic choriomeningitis major depressive disorder mechanical strabismus melancholic depression middle cerebral artery infarction monocular esotropia mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple sclerosis myelitis myocardial infarction narcolepsy nervous system disease neuroblastoma neurodegenerative disease neuromuscular disease neurotic disorder nicotine dependence obsolete constipation obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea olivopontocerebellar atrophy ophthalmoplegia osteoarthritis partial motor epilepsy pathologic nystagmus pellagra peptic esophagitis poliomyelitis polyhydramnios polyneuropathy postinflammatory pulmonary fibrosis primary angle-closure glaucoma progressive bulbar palsy psychotic disorder ptosis pulmonary fibrosis red-green color blindness retinal disease retinitis retrograde amnesia rheumatoid arthritis schizophrenia scoliosis secondary Parkinson disease sensorineural hearing loss silent myocardial infarction situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus sudden infant death syndrome tendinitis thiamine deficiency disease 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 vascular dementia visual epilepsy
1113	chromogranin A	CHGA Aliases: PHE5 PHES pancreastatin parastatin parathyroid secretory protein 1 vasostatin	Homo sapiens (human)	Clostridium difficile colitis Creutzfeldt-Jakob disease Ewing sarcoma IgA glomerulonephritis Peutz-Jeghers syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adult lymphoma amyotrophic lateral sclerosis anxiety disorder aortic atherosclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation atrophic gastritis bladder carcinoma breast cancer breast carcinoma cancer carcinoma cerebral primitive neuroectodermal tumor cervix small cell carcinoma childhood angiosarcoma childhood lymphoma chronic fatigue syndrome chronic kidney disease colitis collagenous colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome dermatitis diabetes mellitus diabetic ketoacidosis diarrhea duodenum cancer embryoma encephalitis encephalomyelitis end stage renal disease endocrine gland cancer esophageal cancer esophageal carcinoma essential hypertension familial adenomatous polyposis follicular adenoma gastrinoma gastroenteritis generalized anxiety disorder granular cell carcinoma heart cancer hypertension hypoglycemia ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease insulinoma intermediate coronary syndrome irritable bowel syndrome islet cell tumor kidney failure large intestine cancer lung cancer lung disease lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphocytic colitis medulloblastoma medulloepithelioma microcystic adenoma multiple sclerosis myelitis myocardial infarction nephrosclerosis neuroblastoma neurocirculatory asthenia neurodegenerative disease neuroectodermal tumor neuroendocrine carcinoma neuroendocrine tumor obesity obsolete dyspepsia obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered osteoarthritis pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenoma paraganglioma periodontitis pheochromocytoma phobic disorder pineal gland cancer pineoblastoma progressive muscular atrophy prolactinoma prostate cancer prostate carcinoma pulmonary embolism pulmonary large cell neuroendocrine carcinoma renal hypertension sarcomatoid carcinoma schizophrenia silent myocardial infarction small intestine cancer squamous cell carcinoma stomach cancer stomach carcinoma supratentorial primitive neuroectodermal tumor thyroid gland medullary carcinoma tongue squamous cell carcinoma transitional cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis ureter small cell carcinoma urinary bladder cancer von Hippel-Lindau disease
1116	chitinase 3 like 1	CHI3L1 Aliases: GP39 YK-40 YKL40 cartilage glycoprotein-39	Homo sapiens (human)	Alexander disease 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma CD40 ligand deficiency Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Gaucher's disease Goodpasture syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hantavirus hemorrhagic fever with renal syndrome Hermansky-Pudlak syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kawasaki disease Kuhnt-Junius degeneration Lafora disease Lewy body dementia Loeffler syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Takayasu's arteritis X-linked hyper IgM syndrome acne acquired immunodeficiency syndrome acrodermatitis actinic keratosis acute chest syndrome acute disseminated encephalomyelitis acute interstitial pneumonia acute kidney tubular necrosis acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenoleukodystrophy adult acute lymphocytic leukemia adult oligodendroglioma age related macular degeneration agnosia alcoholic liver cirrhosis allergic asthma allergic rhinitis alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis anaplastic astrocytoma androgen insensitivity syndrome anemia anthracosilicosis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asthma atherosclerosis atopic dermatitis atrial fibrillation autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy bacterial infectious disease bacterial meningitis bacterial pneumonia bacterial sepsis benign ependymoma bipolar disorder bladder urothelial carcinoma blind loop syndrome bone disease bone marrow cancer bone osteosarcoma brain infarction breast cancer breast carcinoma bronchiolitis obliterans bronchitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma byssinosis cancer cardiovascular system disease carotid artery disease cartilage disease cataract 32 multiple types cellular ependymoma central nervous system cancer central nervous system disease cerebral cavernous malformation 1 cerebral degeneration cerebral infarction cerebral malaria cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia childhood oligodendroglioma childhood osteosarcoma childhood type dermatomyositis chondrosarcoma chromophobe renal cell carcinoma chronic ethmoiditis chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency congestive heart failure connective tissue disease coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma cystic fibrosis degeneration of macula and posterior pole dementia depressive disorder dermatitis dermatomyositis diabetes mellitus diabetic ketoacidosis diabetic macular edema dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health distal arthrogryposis embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma eosinophilic pneumonia epilepsy esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exfoliation syndrome extrinsic allergic alveolitis farmer's lung fatal familial insomnia fibrillary astrocytoma follicular adenoma frontotemporal dementia gallbladder disease gastroenteritis gastrointestinal system cancer gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance granular cell carcinoma granulomatosis with polyangiitis heart disease hematologic cancer hepatitis B hepatitis C hepatitis hepatocellular carcinoma hidradenitis suppurativa hidradenitis high grade glioma human immunodeficiency virus infectious disease hyper IgM syndrome hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease immunodeficiency with hyper IgM type 3 inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intermediate coronary syndrome intermittent claudication interstitial lung disease intrahepatic cholestasis of pregnancy intrinsic asthma invasive ductal carcinoma juvenile pilocytic astrocytoma keratitis keratoconjunctivitis kidney disease large intestine cancer lichen planus liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma macrocytic anemia macular degeneration major depressive disorder malaria malignant astrocytoma melancholic depression melanoma meningitis microcystic adenoma middle cerebral artery infarction mitral valve stenosis mixed glioma mixed oligodendroglioma-astrocytoma multiple myeloma multiple sclerosis myelitis myelofibrosis myeloproliferative neoplasm myocardial infarction myositis myotonic dystrophy type 1 myotonic dystrophy type 2 myxopapillary ependymoma nephritis nephrosis nervous system disease neurodegenerative disease neurogenic arthropathy nonpapillary renal cell carcinoma nutmeg liver obesity obsolete melancholia obsolete ymphosarcoma obstructive sleep apnea oligodendroglioma oophoritis osteoarthritis osteoblastoma osteomyelitis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary ependymoma papillary renal cell carcinoma parametritis parapsoriasis pelvic inflammatory disease peripheral artery disease peripheral vascular disease pilocytic astrocytoma plasmacytoma pneumonia polyarteritis nodosa polycythemia vera polycythemia pompholyx portal vein thrombosis post-vaccinal encephalitis postinflammatory pulmonary fibrosis pre-eclampsia prediabetes syndrome primary cutaneous T-cell non-Hodgkin lymphoma primary pulmonary hypertension prion disease progressive muscular atrophy progressive supranuclear palsy prostate cancer prostate carcinoma protoplasmic astrocytoma psoriasis psychotic disorder pulmonary alveolar proteinosis pulmonary emphysema pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pustulosis of palm and sole pyosalpinx pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinal detachment retinal disease retinitis retrograde amnesia rheumatoid arthritis salpingitis sarcoidosis sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scleroderma scoliosis seborrheic keratosis sepiapterin reductase deficiency sick sinus syndrome silent myocardial infarction skin disease skin melanoma small cell carcinoma speech-language disorder-1 squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic scleroderma tanycytic ependymoma tauopathy temporal arteritis thrombophilia thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma tubular adenocarcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis uterine corpus cancer uveoparotid fever vascular dementia vascular disease vasomotor rhinitis viral pneumonia
1117	chitinase 3 like 2	CHI3L2 Aliases: YKL-39 YKL39	Homo sapiens (human)	amyotrophic lateral sclerosis arthritis arthropathy breast cancer cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma osteoarthritis papillary renal cell carcinoma progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
27159	chitinase acidic	CHIA Aliases: AMCase CHIT2 TSA1902 acidic mammalian chitinase	Homo sapiens (human)	Sjogren's syndrome allergic asthma allergic conjunctivitis allergic rhinitis asthma cryptococcosis dry eye syndrome eosinophilic esophagitis giant papillary conjunctivitis intrinsic asthma keratoconjunctivitis sicca silicosis sinusitis vasomotor rhinitis vernal conjunctivitis xerophthalmia
66005	chitinase domain containing 1	CHID1 Aliases: FLJ42707 MGC3234 SI-CLP stabilin-1 interacting chitinase-like protein	Homo sapiens (human)	bronchitis rheumatoid arthritis
1118	chitinase 1	CHIT1 Aliases: CHI3 CHIT chitotriosidase	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 Bloch-Sulzberger syndrome Creutzfeldt-Jakob disease Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Krabbe disease Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Wolman disease acute myeloid leukemia adrenoleukodystrophy alkaptonuria allergic asthma allergic rhinitis amyloidosis amyotrophic lateral sclerosis ancylostomiasis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascariasis ascaridiasis aspartylglucosaminuria asthma atherosclerosis bacterial sepsis beta thalassemia bone marrow cancer breast cancer breast carcinoma cancer carotid artery thrombosis carotid stenosis cerebral degeneration cerebral infarction cerebrovascular disease childhood type dermatomyositis cholestasis chronic obstructive pulmonary disease chylomicron retention disease colorectal cancer colorectal carcinoma common variable immunodeficiency complement deficiency coronary artery disease cryptococcosis cystic fibrosis dementia dermatomyositis diabetes mellitus diabetic ketoacidosis embryoma essential thrombocythemia eumycotic mycetoma familial combined hyperlipidemia familial mediterranean fever filariasis follicular lymphoma frontotemporal dementia fucosidosis gastritis glomerulonephritis glycoproteinosis hepatitis C hypomelanosis of Ito idiopathic interstitial pneumonia interstitial lung disease intrinsic asthma juvenile rheumatoid arthritis kidney disease large intestine cancer lipid storage disease liver cirrhosis lung disease lysosomal acid lipase deficiency lysosomal storage disease malaria mevalonic aciduria multiple sclerosis myelofibrosis myeloproliferative neoplasm nephritis nephrosis neurodegenerative disease neuropathy nodal marginal zone lymphoma nutmeg liver obesity obstructive sleep apnea ochronosis osteoarthritis peripheral nervous system disease plasmacytoma polycythemia vera polycythemia polyneuropathy postinflammatory pulmonary fibrosis progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pulmonary fibrosis pyoureter sarcoidosis sialuria sickle cell anemia sphingolipidosis steatotic liver disease thalassemia tuberculosis type 2 diabetes mellitus uveoparotid fever vascular dementia vasomotor rhinitis
1119	choline kinase alpha	CHKA Aliases: CKI	Homo sapiens (human)	Duchenne muscular dystrophy T-cell acute lymphoblastic leukemia 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 basal cell carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer colon adenoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital muscular dystrophy distal myopathy embryoma epilepsy esophagus squamous cell carcinoma facioscapulohumeral muscular dystrophy gliosarcoma hematologic cancer hepatitis B hepatocellular carcinoma high grade glioma large intestine cancer limb-girdle muscular dystrophy liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma megaconial type congenital muscular dystrophy microcephaly microphthalmia mixed glioma muscular dystrophy myelomeningocele myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma obsolete Matthew-Wood syndrome 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 ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma prostate cancer prostate carcinoma rippling muscle disease 2 spina bifida squamous cell carcinoma steatotic liver disease tethered spinal cord syndrome tongue squamous cell carcinoma transient cerebral ischemia vertebrobasilar insufficiency
1120	choline kinase beta	CHKB Aliases: CHETK	Homo sapiens (human)	Balo concentric sclerosis Bell's palsy Duchenne muscular dystrophy X-linked dilated cardiomyopathy adrenoleukodystrophy agnosia 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 bronchus cancer bronchus carcinoma campomelic dysplasia central nervous system disease centronuclear myopathy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy craniometaphyseal dysplasia cytochrome-c oxidase deficiency disease developmental coordination disorder dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy inherited metabolic disorder intellectual disability isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy microcephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcolepsy nemaline myopathy 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 recurrent hypersomnia restless legs syndrome rigid spine muscular dystrophy 1 rippling muscle disease 2
140578	chondrolectin	CHODL Aliases: FLJ12627 MT75 PRED12	Homo sapiens (human)	bronchus cancer bronchus carcinoma bulimia nervosa cancer idiopathic scoliosis lung cancer lung carcinoma lung non-small cell carcinoma progressive muscular atrophy spinal muscular atrophy
79586	chondroitin polymerizing factor	CHPF Aliases: CHSY2 CSS2 chondroitin sulfate synthase 2	Homo sapiens (human)	IgA glomerulonephritis cancer central nervous system cancer depressive disorder dysthymic disorder embryoma gliosarcoma high grade glioma major depressive disorder melancholic depression mixed glioma neurotic disorder obsolete melancholia
54480	chondroitin polymerizing factor 2	CHPF2 Aliases: CSGlcA-T ChSy-3 KIAA1402 chondroitin sulfate glucuronyltransferase	Homo sapiens (human)	cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer
56994	choline phosphotransferase 1	CHPT1 Aliases: CPT1 phosphatidylcholine synthesizing enzyme	Homo sapiens (human)	Alzheimer's disease Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease 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 Patau syndrome Pearson syndrome Prader-Willi syndrome Robinow syndrome Schimke immuno-osseous dysplasia Seckel syndrome Silver-Russell syndrome Weissenbacher-Zweymuller syndrome X-linked Aarskog syndrome adenocarcinoma adenoma adult medulloblastoma agranulocytosis attention deficit hyperactivity disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome beta thalassemia bladder carcinoma bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma carnitine palmitoyltransferase II deficiency carpal tunnel syndrome cataract catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system cancer central nervous system lymphoma cervical squamous cell carcinoma childhood medulloblastoma chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congestive heart failure cribriform carcinoma decubitus ulcer depressive disorder diabetes mellitus diarrhea diverticulitis dysthymic disorder embryoma endocarditis endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma essential hypertension follicular adenoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatitis C hepatitis hepatocellular carcinoma hiatus hernia high grade glioma hypertension hypoglycemia infective endocarditis inflammatory bowel disease 1 inflammatory bowel disease islet cell tumor large intestine cancer leukopenia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma mixed glioma multiple myeloma neuroblastoma neurotic disorder neutropenia obesity obsolete melancholia obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic endocrine carcinoma papillary adenoma papillary renal cell carcinoma pathological gambling placental insufficiency post-traumatic stress disorder primary pulmonary hypertension prostate cancer prostate carcinoma psychotic disorder pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal disease rippling muscle disease 2 sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder severe congenital neutropenia sick sinus syndrome squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis substance abuse substance-related disorder systemic primary carnitine deficiency disease thalassemia thyroid gland medullary carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer varicocele very long chain acyl-CoA dehydrogenase deficiency
8534	carbohydrate sulfotransferase 1	CHST1 Aliases: C6ST KSGal6ST Keratan sulfotransferase	Homo sapiens (human)	cataract mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia
9486	carbohydrate sulfotransferase 10	CHST10 Aliases: HNK-1ST	Homo sapiens (human)	Japanese encephalitis dengue disease schizophrenia viral infectious disease yellow fever
50515	carbohydrate sulfotransferase 11	CHST11 Aliases: C4ST C4ST1 C4St-1 HSA269537 chondroitin 4-sulfotransferase 1	Homo sapiens (human)	Barrett's esophagus Costello syndrome Richter's syndrome arthritis arthropathy breast cancer breast carcinoma cancer chronic lymphocytic leukemia hepatocellular carcinoma leukoencephalopathy with vanishing white matter liver cancer osteoarthritis ovarian cancer ovarian carcinoma schizophrenia scoliosis
55501	carbohydrate sulfotransferase 12	CHST12 Aliases: C4S-2 C4ST2 chondroitin 4-sulfotransferase 2	Homo sapiens (human)	hypertension lupus erythematosus systemic lupus erythematosus
166012	carbohydrate sulfotransferase 13	CHST13 Aliases: C4ST3 chondroitin 4-sulfotransferase 3	Homo sapiens (human)	arthritis arthropathy osteoarthritis primary pulmonary hypertension
113189	carbohydrate sulfotransferase 14	CHST14 Aliases: D4ST-1 HD4ST	Homo sapiens (human)	Ehlers-Danlos syndrome musculocontractural type 1 Ehlers-Danlos syndrome Marfan syndrome Peters anomaly agnosia arthropathy 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 brittle cornea syndrome 1 cleft palate clubfoot congenital diaphragmatic hernia cornea plana craniosynostosis cryptorchidism developmental coordination disorder distal arthrogryposis familial nephrotic syndrome familial periodic paralysis glaucoma hiatus hernia hydrocephalus hydronephrosis hypertropia isolated cleft palate lipoid nephrosis mechanical strabismus myopathy myopia nephrotic syndrome obsolete constipation omphalocele ophthalmoplegia osteogenesis imperfecta patent foramen ovale pneumothorax prostate cancer prostate carcinoma retinal detachment scoliosis sensorineural hearing loss situs inversus strabismus tuberous sclerosis umbilical hernia
51363	carbohydrate sulfotransferase 15	CHST15 Aliases: B cell RAG associated protein BRAG GALNAC4S-6ST KIAA0598 N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase	Homo sapiens (human)	Crohn's colitis Crohn's disease adult astrocytic tumor anaplastic astrocytoma breast cancer breast carcinoma cancer childhood astrocytic tumor childhood cerebral astrocytoma colitis embryoma endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma giant cell glioblastoma glioblastoma high grade glioma idiopathic interstitial pneumonia ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease juvenile pilocytic astrocytoma lung benign neoplasm malignant astrocytoma microphthalmia obsolete Matthew-Wood syndrome ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma patent ductus arteriosus pilocytic astrocytoma postinflammatory pulmonary fibrosis protoplasmic astrocytoma pulmonary fibrosis subependymal giant cell astrocytoma ulcerative colitis uterine corpus cancer
9435	carbohydrate sulfotransferase 2	CHST2 Aliases: C6ST	Homo sapiens (human)	amyotrophic lateral sclerosis bone osteosarcoma cancer extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue gastric lymphoma inflammatory bowel disease 1 inflammatory bowel disease osteosarcoma progressive muscular atrophy ulcerative colitis
9469	carbohydrate sulfotransferase 3	CHST3 Aliases: C6ST C6ST1 chondroitin 6 sulfotransferase 1	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Bartter disease Conn's syndrome Cowden syndrome Desbuquois dysplasia Hailey-Hailey disease Laron syndrome Larsen syndrome Larsen-like syndrome B3GAT3 type Ollier disease Rothmund-Thomson syndrome SOST-related sclerosing bone dysplasia Schwartz-Jampel syndrome 1 Silverman-Handmaker type dyssegmental dysplasia Sjogren's syndrome Waterhouse-Friderichsen syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia acute promyelocytic leukemia adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adrenoleukodystrophy adult fibrosarcoma agnosia alcoholic hepatitis alcoholic liver cirrhosis amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve insufficiency aortic valve stenosis apparent mineralocorticoid excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis 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 atrophy of testis autoimmune hepatitis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease blastomycosis breast cancer breast carcinoma buphthalmos cancer cardiomyopathy cardiovascular system disease choriocarcinoma cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital adrenal hyperplasia coronary artery disease craniosynostosis cutis laxa cystadenoma dermatitis developmental coordination disorder diabetes mellitus diabetic ketoacidosis diastrophic dysplasia embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis enterocele esotropia essential hypertension fibrosarcoma follicular adenoma heart disease hepatitis hereditary multiple exostoses humeroradial synostosis hydrocephalus hydrophthalmos hyperopia hypertension hypertrophic cardiomyopathy hypogonadotropic hypogonadism 23 with or without anosmia inclusion body myositis intrahepatic cholestasis isolated cleft palate juvenile glaucoma keratoconjunctivitis sicca leiomyoma liver cirrhosis lung small cell carcinoma mal de Meleda microcystic adenoma mitral valve insufficiency mitral valve prolapse mitral valve stenosis monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia myofibroma neurogenic arthropathy obesity obsolete type 1 diabetes mellitus 9 obstructive hydrocephalus osteochondrodysplasia osteoporosis ovarian cancer ovarian carcinoma ovarian hyperstimulation syndrome papillary adenoma paracoccidioidomycosis patent foramen ovale placenta cancer polycystic ovary syndrome postural orthostatic tachycardia syndrome primary hyperaldosteronism primary pulmonary hypertension progressive familial intrahepatic cholestasis progressive pseudorheumatoid arthropathy of childhood pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss spondyloepiphyseal dysplasia congenita spondyloepiphyseal dysplasia with congenital joint dislocations strabismic amblyopia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tricuspid valve insufficiency tricuspid valve stenosis 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 uterine corpus cancer uterine fibroid varicose veins ventricular septal defect
10164	carbohydrate sulfotransferase 4	CHST4 Aliases: HEC-GLCNAC-6-ST LSST	Homo sapiens (human)	arthritis arthropathy cancer colitis colon cancer colon carcinoma colon mucinous adenocarcinoma colonic benign neoplasm colorectal cancer gastroenteritis ileitis ileocolitis large intestine cancer osteoarthritis
23563	carbohydrate sulfotransferase 5	CHST5 Aliases: FLJ22167 I-GLCNAC-6-ST	Homo sapiens (human)	adenocarcinoma adenoma cribriform carcinoma granular cell carcinoma tubular adenocarcinoma
4166	carbohydrate sulfotransferase 6	CHST6	Homo sapiens (human)	age related macular degeneration amyloidosis corneal dystrophy degeneration of macula and posterior pole granular corneal dystrophy macular corneal dystrophy macular degeneration obsolete asthenopia recurrent corneal erosion

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