GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
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GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **12451 - 12475** of **126547** in total

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UniProt ID	Protein Name ▲	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q6PGK7	Carbohydrate sulfotransferase 10	Chst10	Mus musculus (house mouse)	3	0
Q5RBZ6	Carbohydrate sulfotransferase 10	CHST10	Pongo abelii (Sumatran orangutan)	3	0
O54702	Carbohydrate sulfotransferase 10	Chst10	Rattus norvegicus (Norway rat)	3	0
P69478	Carbohydrate sulfotransferase 11	Chst11	Rattus norvegicus (Norway rat)	4	0
Q7T3S3	Carbohydrate sulfotransferase 11	chst11	Danio rerio (zebrafish)	4	0
Q9JME2	Carbohydrate sulfotransferase 11	Chst11	Mus musculus (house mouse)	4	0
Q9NPF2	Carbohydrate sulfotransferase 11	CHST11	Homo sapiens (human)	5	3	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
Q99LL3	Carbohydrate sulfotransferase 12	Chst12	Mus musculus (house mouse)	4	0
Q9NRB3	Carbohydrate sulfotransferase 12	CHST12	Homo sapiens (human)	7	5	lupus erythematosus systemic lupus erythematosus
Q5XHM7	Carbohydrate sulfotransferase 12	chst12	Xenopus laevis (African clawed frog)	5	0
Q8NET6	Carbohydrate sulfotransferase 13	CHST13	Homo sapiens (human)	1	0	arthritis arthropathy osteoarthritis primary pulmonary hypertension
Q8NCH0	Carbohydrate sulfotransferase 14	CHST14 D4ST1	Homo sapiens (human)	6	4	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
Q80V53	Carbohydrate sulfotransferase 14	Chst14 D4st1	Mus musculus (house mouse)	2	0
Q805E5	Carbohydrate sulfotransferase 14	chst14 d4st1	Danio rerio (zebrafish)	2	0
Q91XQ5	Carbohydrate sulfotransferase 15	Chst15 Brag Galnac4s6st Kiaa0598	Mus musculus (house mouse)	5	0
Q7LFX5	Carbohydrate sulfotransferase 15	CHST15 BRAG GALNAC4S6ST KIAA0598	Homo sapiens (human)	4	2	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
Q8CHI9	Carbohydrate sulfotransferase 15	Chst15 Galnac4s6st	Rattus norvegicus (Norway rat)	1	0
Q8WTN9	Carbohydrate sulfotransferase 15 (Fragments)	GALNAC4S6ST	Nototodarus sloanii (Sloane's squid)	2	0
Q9Y4C5	Carbohydrate sulfotransferase 2	CHST2 GN6ST	Homo sapiens (human)	4	1	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
Q80WV3	Carbohydrate sulfotransferase 2	Chst2 Gst2	Mus musculus (house mouse)	4	0
Q92179	Carbohydrate sulfotransferase 3	CHST3	Gallus gallus (chicken)	6	0
Q9QZL2	Carbohydrate sulfotransferase 3	Chst3	Rattus norvegicus (Norway rat)	6	0
O88199	Carbohydrate sulfotransferase 3	Chst3 C6st Gst0	Mus musculus (house mouse)	6	0
Q7LGC8	Carbohydrate sulfotransferase 3	CHST3	Homo sapiens (human)	6	4	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
O93403	Carbohydrate sulfotransferase 3	CHST3 NSIST	Tetronarce californica (Pacific electric ray)	4	0

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