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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 **1026 - 1050** of **1582** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
78989	collectin subfamily member 11	COLEC11 Aliases: CL-11 CL-K1 Collectin K1 MGC3279	Homo sapiens (human)	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC syndrome Bloch-Sulzberger syndrome Chagas disease Klippel-Feil syndrome acquired immunodeficiency syndrome bacterial infectious disease bacterial sepsis blepharophimosis cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism disseminated intravascular coagulation enterobiasis glomerulonephritis human immunodeficiency virus infectious disease humeroradial synostosis hypertropia hypomelanosis of Ito intellectual disability intestinal schistosomiasis isolated cleft palate kidney disease learning disability mechanical strabismus nephritis nephrosis neurodegenerative disease omphalocele ophthalmoplegia pneumonia ptosis purpura fulminans pyoureter radioulnar synostosis schistosomiasis scoliosis sensorineural hearing loss spina bifida occulta spondylolisthesis strabismus trichinosis trypanosomiasis tuberculosis umbilical hernia urinary schistosomiasis viral infectious disease
10584	collectin subfamily member 10	COLEC10 Aliases: CL-10 CL-L1	Homo sapiens (human)	3MC syndrome 3 3MC syndrome Klippel-Feil syndrome Laron syndrome Richter's syndrome achondroplasia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia allergic asthma asthma basal cell carcinoma blepharophimosis cancer carcinoma chronic lymphocytic leukemia cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism essential thrombocythemia hepatocellular carcinoma humeroradial synostosis intellectual disability isolated cleft palate learning disability liver cancer lymphoblastic lymphoma lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma omphalocele ptosis radioulnar synostosis scoliosis sebaceous carcinoma sensorineural hearing loss spina bifida occulta spondylolisthesis sweat gland cancer umbilical hernia
1291	collagen type VI alpha 1 chain	COL6A1	Homo sapiens (human)	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
1298	collagen type IX alpha 2 chain	COL9A2 Aliases: MED	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Dowling-Degos disease Ehlers-Danlos syndrome Laron syndrome Laurin-Sandrow syndrome Osgood-Schlatter's disease Stickler syndrome achondroplasia acrodermatitis adult medulloblastoma allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia alternating hemiplegia of childhood amblyopia arthritis arthropathy asthma astigmatism atrial fibrillation autonomic neuropathy bone disease bone osteosarcoma cancer cardiovascular system disease cartilage disease cataract central nervous system cancer central nervous system disease childhood medulloblastoma childhood osteosarcoma chondrodysplasia punctata chronic kidney disease cleft palate collagen disease connective tissue disease degenerative disc disease depressive disorder dermatitis diabetes mellitus diastrophic dysplasia disease of metabolism dysplastic nevus syndrome dysthymic disorder epithelioid sarcoma essential hypertension eye disease familial hypercholesterolemia familial mediterranean fever familial periodic paralysis gliosarcoma granuloma annulare heart disease hemoglobin H disease high grade glioma hypertension intrinsic asthma isolated cleft palate major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mevalonic aciduria mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia 2 multiple epiphyseal dysplasia myopathy myopia nervous system disease neurotic disorder obsolete melancholia osteoarthritis osteochondritis dissecans osteochondrodysplasia osteochondrosis osteogenesis imperfecta osteosarcoma pancreatic ductal adenocarcinoma pseudoachondroplasia reticulate acropigmentation of Kitamura retinal detachment rheumatoid arthritis sarcoma sensorineural hearing loss spinal stenosis spindle cell sarcoma strabismic amblyopia thalassemia thoracic aortic aneurysm type 2 diabetes mellitus
23127	collagen beta(1-O)galactosyltransferase 2	COLGALT2 Aliases: KIAA0584 Procollagen galactosyltransferase	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 Pick's disease Reye syndrome bone osteosarcoma breast cancer cerebral degeneration hepatitis A hepatitis lung benign neoplasm osteoarthritis osteosarcoma
79709	collagen beta(1-O)galactosyltransferase 1	COLGALT1 Aliases: FLJ22329 Hydroxylysine galactosyltransferase Procollagen galactosyltransferase	Homo sapiens (human)	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma brain small vessel disease 3 central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
84317	coiled-coil domain containing 115	CCDC115 Aliases: FLJ30131 MGC12981 ccp1	Homo sapiens (human)	Wilson disease cancer congenital disorder of glycosylation type IIo congenital disorder of glycosylation gallbladder disease hemochromatosis iron metabolism disease liver disease male infertility measles neuroblastoma neurodegenerative disease prostate adenocarcinoma prostate cancer prostate carcinoma
51805	coenzyme Q3, methyltransferase	COQ3	Homo sapiens (human)
27235	coenzyme Q2, polyprenyltransferase	COQ2	Homo sapiens (human)	coenzyme Q10 deficiency disease glucose intolerance multiple system atrophy nephrotic syndrome primary coenzyme Q10 deficiency 1
1431	citrate synthase	CS	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 Brill-Zinsser disease Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Pick's disease Poland syndrome Q fever Reye syndrome Sengers syndrome Siberian tick typhus Zollinger-Ellison syndrome adrenal gland cancer amyotrophic lateral sclerosis anaplastic astrocytoma autism spectrum disorder autistic disorder bacillary angiomatosis bacterial sepsis bipolar disorder cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral degeneration childhood cerebral astrocytoma chronic obstructive pulmonary disease congestive heart failure coronary artery disease depressive disorder dermoid cyst of ovary diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy duodenum cancer dysthymic disorder embryoma endocarditis endomyocardial fibrosis fibrillary astrocytoma gangliocytoma ganglioneuroma gemistocytic astrocytoma giant cell glioblastoma glioblastoma heart cancer high grade glioma hyperinsulinism hyperthyroidism hypertrophic cardiomyopathy hypothyroidism juvenile pilocytic astrocytoma limb ischemia major depressive disorder malaria malignant astrocytoma melancholic depression mitochondrial DNA depletion syndrome 12b mitochondrial DNA depletion syndrome mitochondrial metabolism disease mitochondrial myopathy myocardial infarction myofibrillar myopathy neuroblastoma neurotic disorder obesity obsolete melancholia obsolete ymphosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma parapsoriasis peripheral artery disease pheochromocytoma pilocytic astrocytoma primary pulmonary hypertension progressive muscular atrophy protoplasmic astrocytoma psoriasis pustulosis of palm and sole retinal degeneration rickettsialpox small intestine cancer spondylocarpotarsal synostosis syndrome spotted fever steatotic liver disease subependymal giant cell astrocytoma thyrotoxicosis trypanosomiasis type 2 diabetes mellitus typhus
1271	ciliary neurotrophic factor receptor	CNTFR	Homo sapiens (human)	acute lymphoblastic leukemia adult acute lymphocytic leukemia amyotrophic lateral sclerosis attention deficit hyperactivity disorder cancer central nervous system cancer childhood acute lymphocytic leukemia childhood acute myeloid leukemia cold-induced sweating syndrome 1 cold-induced sweating syndrome gliosarcoma high grade glioma idiopathic scoliosis mixed glioma myasthenia gravis progressive muscular atrophy rheumatoid arthritis
140873	chromosome 20 open reading frame 173	C20orf173 Aliases: dJ477O4.4	Homo sapiens (human)
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
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
337876	chondroitin sulfate synthase 3	CHSY3 Aliases: CHSY-2 CSS3	Homo sapiens (human)	breast cancer central nervous system cancer colorectal cancer colorectal carcinoma gliosarcoma high grade glioma large intestine cancer mixed glioma pancreatic cancer pancreatic carcinoma
22856	chondroitin sulfate synthase 1	CHSY1 Aliases: CSS1 KIAA0990	Homo sapiens (human)	Laron syndrome X-linked nonsyndromic deafness achondroplasia adult malignant schwannoma anodontia autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness breast cancer breast carcinoma cancer childhood malignant schwannoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma embryoma epithelioid malignant peripheral nerve sheath tumor epithelioid sarcoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma large intestine cancer liver cancer malignant peripheral nerve sheath tumor myxofibrosarcoma neurilemmoma neurofibrosarcoma neuropathy nonpapillary renal cell carcinoma obsolete autosomal recessive nonsyndromic deafness 105 optic atrophy papillary renal cell carcinoma peripheral nervous system disease renal carcinoma renal cell carcinoma sarcoma sarcomatoid renal cell carcinoma spindle cell sarcoma syndactyly temtamy preaxial brachydactyly syndrome tooth agenesis
10675	chondroitin sulfate proteoglycan 5	CSPG5 Aliases: NGC neuroglycan C	Homo sapiens (human)	Beckwith-Wiedemann syndrome CLOVES syndrome Japanese encephalitis Perlman syndrome Sotos syndrome dengue disease schizophrenia viral infectious disease yellow fever
1464	chondroitin sulfate proteoglycan 4	CSPG4 Aliases: CSPG4A HMW-MAA MCSP MCSPG MEL-CSPG MSK16 NG2 melanoma-associated chondroitin sulfate proteoglycan	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 Pick's disease Reye syndrome Richter's syndrome Ullrich congenital muscular dystrophy X-linked ichthyosis acute lymphoblastic leukemia adult oligodendroglioma angiomyolipoma arthritis arthropathy benign mesothelioma bone osteosarcoma brain cancer brain ischemia breast cancer breast carcinoma cancer central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood oligodendroglioma childhood osteosarcoma chondrosarcoma chordoma chronic lymphocytic leukemia colitis congenital merosin-deficient muscular dystrophy 1A dementia depressive disorder dysplastic nevus syndrome dysthymic disorder embryoma endometrial cancer endometrial carcinoma epithelioid sarcoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma ileitis ileocolitis leukemia liver cancer lymphoblastic lymphoma major depressive disorder malignant mesothelioma melancholic depression melanoma mixed glioma mixed oligodendroglioma-astrocytoma neurotic disorder obsolete melancholia obsolete ymphosarcoma obstructive sleep apnea oligodendroglioma osteoarthritis osteosarcoma pancreatic cancer relapsing-remitting multiple sclerosis sarcoma schizophrenia skin melanoma spindle cell sarcoma uterine corpus cancer
55454	chondroitin sulfate N-acetylgalactosaminyltransferase 2	CSGALNACT2 Aliases: GALNACT-2 GALNACT2 MGC40204 PRO0082 chondroitin beta1,4 N-acetylgalactosaminyltransferase 2 glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase 2	Homo sapiens (human)	Hirschsprung's disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis multiple sclerosis
55790	chondroitin sulfate N-acetylgalactosaminyltransferase 1	CSGALNACT1 Aliases: CSGalNAcT-1 ChGn FLJ11264 chondroitin beta1,4 N-acetylgalactosaminyltransferase glucuronylgalactosylproteoglycan 4-beta-N- acetylgalactosaminyltransferase	Homo sapiens (human)	Guillain-Barre syndrome Laron syndrome Miller Fisher syndrome achondroplasia anorexia nervosa breast cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetic ketoacidosis large intestine cancer melanoma multiple sclerosis obsolete type 1 diabetes mellitus 9 skin melanoma 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
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
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
10390	choline/ethanolamine phosphotransferase 1	CEPT1	Homo sapiens (human)	diabetic ketoacidosis obesity obsolete type 1 diabetes mellitus 9 retinal disease systemic lupus erythematosus 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
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
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

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