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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 **1076 - 1100** of **1582** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
1374	carnitine palmitoyltransferase 1A	CPT1A Aliases: CPT1-L L-CPT1	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 D-bifunctional protein deficiency Niemann-Pick disease type C1 Niemann-Pick disease Pearson syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction alcoholic hepatitis alveolar rhabdomyosarcoma amnestic disorder beta thalassemia breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency cataract 4 multiple types cerebral degeneration chronic fatigue syndrome chronic kidney disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential thrombocythemia familial hyperlipidemia familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease isolated elevated serum creatine phosphokinase levels large intestine cancer lipid metabolism disorder liver cancer liver carcinoma liver cirrhosis lymphangioleiomyomatosis major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma metabolic dysfunction-associated steatohepatitis mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction nasopharynx carcinoma neurotic disorder obesity obsolete melancholia osteoporosis placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis renal tubular acidosis retrograde amnesia sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction skin melanoma speech disorder steatotic liver disease stomach cancer stomach carcinoma sudden infant death syndrome systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency visual epilepsy
54675	cardiolipin synthase 1	CRLS1 Aliases: CLS1 GCD10 GCD10 homolog (S. cerevisiae) dJ967N21.6	Homo sapiens (human)	Coffin-Lowry syndrome adenosarcoma bilateral breast cancer breast cancer breast ductal carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma cancer colitis combined oxidative phosphorylation deficiency 57 depressive disorder dysthymic disorder gastroenteritis hepatitis C hepatocellular carcinoma ileitis ileocolitis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder mastitis melancholic depression microglandular adenosis nephroblastoma neurotic disorder obsolete melancholia paroxysmal nocturnal hemoglobinuria schizophrenia vascular dementia
130749	carboxypeptidase O	CPO Aliases: metallocarboxypeptidase C metallocarboxypeptidase O	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 DiGeorge syndrome Pick's disease Reye syndrome Van der Woude syndrome cerebral degeneration colorectal cancer colorectal carcinoma craniosynostosis hereditary coproporphyria large intestine cancer melorheostosis velocardiofacial syndrome
1368	carboxypeptidase M	CPM Aliases: renal carboxypeptidase urinary carboxypeptidase B	Homo sapiens (human)	adult liposarcoma anthracosilicosis anxiety disorder aphasia asbestosis atrial fibrillation breast cancer breast carcinoma cancer childhood liposarcoma colorectal cancer colorectal carcinoma embryoma endometriosis of ovary endometriosis generalized anxiety disorder inflammatory liposarcoma kidney failure large intestine cancer lipoma liposarcoma lung adenocarcinoma lung cancer multiple symmetric lipomatosis pleomorphic lipoma pleomorphic liposarcoma proliferative diabetic retinopathy sclerosing liposarcoma silicosis well-differentiated liposarcoma
1056	carboxyl ester lipase	CEL	Homo sapiens (human)	B-cell lymphoma Bloch-Sulzberger syndrome Goodpasture syndrome Loeffler syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Takayasu's arteritis Wolman disease X-linked chronic granulomatous disease acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute pancreatitis adamantinous craniopharyngioma adenocarcinoma adenoma adiposis dolorosa adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome aggressive systemic mastocytosis agranulocytosis alcoholic liver cirrhosis alcoholic pancreatitis allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma ataxic cerebral palsy atherosclerosis autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease bone marrow cancer brain disease breast cancer breast carcinoma bronchiectasis cancer central nervous system lymphoma childhood acute lymphocytic leukemia childhood lymphoma chronic eosinophilic leukemia chronic granulomatous disease chronic neutrophilic leukemia chronic obstructive pulmonary disease complement deficiency coronary artery disease craniopharyngioma cribriform carcinoma cutaneous porphyria cystic fibrosis cystic kidney disease diabetes mellitus diabetic ketoacidosis embryoma eosinophilic pneumonia epithelioid sarcoma erythropoietic protoporphyria exocrine pancreatic insufficiency extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue extrinsic allergic alveolitis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperlipidemia farmer's lung gastric lymphoma giardiasis glomerulonephritis granular cell carcinoma granulomatosis with polyangiitis hematologic cancer hepatitis C hepatitis hepatocellular carcinoma histoplasmosis hypereosinophilic syndrome hyperglycemia hyperinsulinemic hypoglycemia hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis indolent systemic mastocytosis influenza interstitial lung disease intrinsic asthma kidney disease kwashiorkor leukopenia lipid storage disease lipomatosis liver cancer lung disease lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 lysosomal acid lipase deficiency malaria marasmus mastocytosis maturity-onset diabetes of the young type 8 maturity-onset diabetes of the young microphthalmia multiple symmetric lipomatosis myeloproliferative neoplasm nasopharynx carcinoma nephritis nephrosis neurofibromatosis 1 neurofibromatosis neutropenia newborn respiratory distress syndrome non-congenital cyst of kidney nutmeg liver nutrition disease obesity obsolete Matthew-Wood syndrome obsolete multiple symmetrical lipomatosis obsolete ymphosarcoma pancreas disease pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis papillary craniopharyngioma placental insufficiency plasmacytoma pneumocystosis pneumonia polyarteritis nodosa polycythemia vera polycythemia postinflammatory pulmonary fibrosis primary ciliary dyskinesia 1 primary ciliary dyskinesia protein-energy malnutrition pulmonary alveolar proteinosis pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pyoureter red-green color blindness retinal disease retinitis sarcoidosis sarcoma scleroderma severe congenital neutropenia spindle cell sarcoma steatotic liver disease substance abuse substance-related disorder systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic mastocytosis systemic scleroderma tuberculosis tuberculous pneumothorax tubular adenocarcinoma type 1 diabetes mellitus type 2 diabetes mellitus uveoparotid fever
84869	carbonyl reductase 4	CBR4 Aliases: FLJ14431 SDR45C1 short chain dehydrogenase/reductase family 45C, member 1	Homo sapiens (human)	biliary atresia pancreatic cancer tuberculosis
874	carbonyl reductase 3	CBR3 Aliases: SDR21C2 short chain dehydrogenase/reductase family 21C, member 2	Homo sapiens (human)	acute myeloid leukemia bone osteosarcoma breast cancer breast carcinoma cancer cardiomyopathy childhood osteosarcoma congestive heart failure diabetes mellitus endomyocardial fibrosis familial retinoblastoma hypertrophic cardiomyopathy osteosarcoma ovarian cancer ovarian carcinoma retinoblastoma trilateral retinoblastoma type 2 diabetes mellitus
873	carbonyl reductase 1	CBR1 Aliases: SDR21C1 short chain dehydrogenase/reductase family 21C, member 1	Homo sapiens (human)	Crohn's colitis Crohn's disease Down syndrome Marfan syndrome acute myeloid leukemia acute promyelocytic leukemia adenocarcinoma adenoma amyotrophic lateral sclerosis bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiomyopathy cervical cancer cholangiocarcinoma chordoma chorioamnionitis chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma decubitus ulcer diabetes mellitus diabetic ketoacidosis embryoma endomyocardial fibrosis familial adenomatous polyposis 1 familial adenomatous polyposis gastric tubular adenocarcinoma gastrointestinal system cancer giant cell glioblastoma glioblastoma glucocorticoid-remediable aldosteronism glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease 1 inflammatory bowel disease intracranial aneurysm intrahepatic cholangiocarcinoma irritant dermatitis islet cell tumor large intestine cancer leukemia liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lung squamous cell carcinoma obesity obsolete type 1 diabetes mellitus 9 ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma prediabetes syndrome primary hypertrophic osteoarthropathy progressive muscular atrophy prostate cancer prostate carcinoma sarcomatoid carcinoma secondary hypertrophic osteoarthropathy situs inversus steatotic liver disease stomach cancer stomach carcinoma thyroid gland medullary carcinoma tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis 1 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 ureteral obstruction uterus leiomyosarcoma vitiligo
762	carbonic anhydrase 4	CA4 Aliases: CAIV Car4	Homo sapiens (human)	Behcet's disease Zollinger-Ellison syndrome achromatopsia acquired color blindness blindness blue color blindness brain cancer cancer cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease diabetes mellitus dissociated nystagmus eye disease fundus albipunctatus glaucoma hyperinsulinism hypogonadism intellectual disability keratoconus large intestine cancer learning disability lung cancer lung non-small cell carcinoma myocarditis night blindness nonpapillary renal cell carcinoma obesity obsolete asthenopia ophthalmoplegia optic atrophy papillary renal cell carcinoma pathologic nystagmus red color blindness red-green color blindness renal carcinoma renal cell carcinoma retinitis pigmentosa 17 retinitis pigmentosa sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus type 2 diabetes mellitus
83539	carbohydrate sulfotransferase 9	CHST9 Aliases: GALNAC-4-ST2 GALNAC4ST-2	Homo sapiens (human)	acute lymphoblastic leukemia acute myeloid leukemia breast cancer breast carcinoma cancer coronary artery disease depressive disorder essential thrombocythemia hematologic cancer idiopathic scoliosis lymphoblastic lymphoma major depressive disorder melancholic depression myelodysplastic syndrome obsolete melancholia schizophrenia
64377	carbohydrate sulfotransferase 8	CHST8 Aliases: GALNAC4ST-1	Homo sapiens (human)	allergic asthma asthma atopic dermatitis colorectal cancer colorectal carcinoma intrinsic asthma large intestine cancer parapsoriasis peeling skin syndrome psoriasis pustulosis of palm and sole scleroderma skin disease systemic scleroderma
56548	carbohydrate sulfotransferase 7	CHST7 Aliases: C6ST-2 C6ST2	Homo sapiens (human)	bronchus cancer bronchus carcinoma colorectal cancer colorectal carcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma pneumonia
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
23563	carbohydrate sulfotransferase 5	CHST5 Aliases: FLJ22167 I-GLCNAC-6-ST	Homo sapiens (human)	adenocarcinoma adenoma cribriform carcinoma granular cell carcinoma tubular adenocarcinoma
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
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
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
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
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
166012	carbohydrate sulfotransferase 13	CHST13 Aliases: C4ST3 chondroitin 4-sulfotransferase 3	Homo sapiens (human)	arthritis arthropathy osteoarthritis primary pulmonary hypertension
55501	carbohydrate sulfotransferase 12	CHST12 Aliases: C4S-2 C4ST2 chondroitin 4-sulfotransferase 2	Homo sapiens (human)	hypertension lupus erythematosus systemic lupus erythematosus
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
9486	carbohydrate sulfotransferase 10	CHST10 Aliases: HNK-1ST	Homo sapiens (human)	Japanese encephalitis dengue disease schizophrenia viral infectious disease yellow fever
8534	carbohydrate sulfotransferase 1	CHST1 Aliases: C6ST KSGal6ST Keratan sulfotransferase	Homo sapiens (human)	cataract mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia
9746	calsyntenin 3	CLSTN3	Homo sapiens (human)

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