GlyCosmos Portal

GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen, GlyConnect, GlycoProtDB and The O-GlcNAc Database. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **1826 - 1850** of **18496** in total

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UniProt ID	Protein Name ▲	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P31327	Carbamoyl-phosphate synthase [ammonia], mitochondrial	CPS1	Homo sapiens (human)	7	5
A0A7S9TQK2	Carbocypeptidase E	CPE	Homo sapiens (human)	1	0
C9J991	Carbohydrate sulfotransferase (Fragment)	CHST12	Homo sapiens (human)	1	0
O43916	Carbohydrate sulfotransferase 1	CHST1	Homo sapiens (human)	4	0	cataract mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia
O43529	Carbohydrate sulfotransferase 10	CHST10	Homo sapiens (human)	5	3	Japanese encephalitis dengue disease schizophrenia viral infectious disease yellow fever
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
Q9NRB3	Carbohydrate sulfotransferase 12	CHST12	Homo sapiens (human)	7	5	lupus erythematosus systemic lupus erythematosus
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
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
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
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
Q8NCG5	Carbohydrate sulfotransferase 4	CHST4	Homo sapiens (human)	3	0	arthritis arthropathy cancer colitis colon cancer colon carcinoma colon mucinous adenocarcinoma colonic benign neoplasm colorectal cancer gastroenteritis ileitis ileocolitis large intestine cancer osteoarthritis
Q9GZS9	Carbohydrate sulfotransferase 5	CHST5	Homo sapiens (human)	3	1	adenocarcinoma adenoma cribriform carcinoma granular cell carcinoma tubular adenocarcinoma
Q9GZX3	Carbohydrate sulfotransferase 6	CHST6	Homo sapiens (human)	4	1	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
Q9NS84	Carbohydrate sulfotransferase 7	CHST7	Homo sapiens (human)	4	4	bronchus cancer bronchus carcinoma colorectal cancer colorectal carcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma pneumonia
Q9H2A9	Carbohydrate sulfotransferase 8	CHST8	Homo sapiens (human)	8	1	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
Q7L1S5	Carbohydrate sulfotransferase 9	CHST9	Homo sapiens (human)	7	5	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
Q9NP71	Carbohydrate-responsive element-binding protein	MLXIPL BHLHD14 MIO WBSCR14	Homo sapiens (human)	8	1
P00915	Carbonic anhydrase 1	CA1	Homo sapiens (human)	2	1
O43570	Carbonic anhydrase 12	CA12	Homo sapiens (human)	3	1
Q9ULX7	Carbonic anhydrase 14	CA14	Homo sapiens (human)	1	0
P00918	Carbonic anhydrase 2	CA2	Homo sapiens (human)	0	1
P07451	Carbonic anhydrase 3	CA3	Homo sapiens (human)	0	1
Q9Y2D0	Carbonic anhydrase 5B, mitochondrial	CA5B	Homo sapiens (human)	1	1

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