GlyCosmos Portal

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 **15751 - 15775** 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
Q5TEA6	Protein sel-1 homolog 2	SEL1L2 C20orf50	Homo sapiens (human)	1	0
P04278	Sex hormone-binding globulin	SHBG	Homo sapiens (human)	3	23
Q8TC27	Disintegrin and metalloproteinase domain-containing protein 32	ADAM32	Homo sapiens (human)	4	0
Q71SW6	Neuropilin	NRP1	Homo sapiens (human)	2	0
O95256	Interleukin-18 receptor accessory protein	IL18RAP IL1R7	Homo sapiens (human)	4	0	Bannayan-Riley-Ruvalcaba syndrome Burkitt lymphoma Cowden syndrome Crohn's colitis Crohn's disease Graves' disease Richter's syndrome allergic asthma asthma autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis bone marrow disease cancer cardiovascular system disease celiac disease cerebral infarction cerebrovascular disease chronic lymphocytic leukemia degenerative disc disease diabetic ketoacidosis esophageal disease essential hypertension goiter heart disease hypertension hyperthyroidism immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma obsolete type 1 diabetes mellitus 9 rheumatoid arthritis spinal cord disease stomach disease syringomyelia systemic lupus erythematosus thyroid gland disease thyrotoxicosis 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 ulcerative colitis
P00387	NADH-cytochrome b5 reductase 3	CYB5R3 DIA1	Homo sapiens (human)	3	2	acquired polycythemia alternating hemiplegia of childhood autonomic neuropathy bladder urothelial carcinoma brain disease breast cancer breast carcinoma cancer central nervous system disease colon cancer colonic benign neoplasm colorectal cancer contagious pustular dermatitis cowpox dystonia embryoma epilepsy erythema infectiosum erythropoietin polycythemia esotropia essential hypertension exanthema subitum familial erythrocytosis 2 familial hyperlipidemia hypertension hypertropia idiopathic scoliosis intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia locked-in syndrome maple syrup urine disease mechanical strabismus methemoglobinemia microcephaly milker's nodule monocular esotropia movement disease nervous system disease ophthalmoplegia placental insufficiency polycythemia vera polycythemia quadriplegia sickle cell anemia smallpox strabismus stress polycythemia sulfhemoglobinemia syndromic X-linked intellectual disability 94 tarsal-carpal coalition syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma variola major variola minor visual epilepsy
Q9Y487	V-type proton ATPase 116 kDa subunit a 2	ATP6V0A2	Homo sapiens (human)	5	7	Crohn's colitis Crohn's disease Dandy-Walker syndrome Ehlers-Danlos syndrome Hailey-Hailey disease Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Rothmund-Thomson syndrome achondroplasia agnosia alopecia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 autosomal recessive osteopetrosis 7 bacterial sepsis bicuspid aortic valve disease bone disease breast cancer breast carcinoma cancer cartilage disease clubfoot complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease coronary artery disease cortical dysplasia-focal epilepsy syndrome cryptococcosis cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder diabetic cataract diabetic retinopathy encephalitis encephalomyelitis epilepsy essential hypertension generalized atherosclerosis geroderma osteodysplasticum giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hydranencephaly hypertension hypertropia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intracranial aneurysm learning disability lipoatrophic diabetes mellitus lipodystrophy lissencephaly lung disease mal de Meleda male infertility mechanical strabismus microcephaly mixed glioma myelitis myopia omphalocele ophthalmoplegia osteogenesis imperfecta osteopetrosis osteosclerosis placental insufficiency platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pulmonary emphysema renal tubular acidosis restrictive dermopathy scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly status epilepticus strabismus syndromic X-linked intellectual disability Najm type ulcerative colitis umbilical hernia visual epilepsy von Willebrand's disease
Q9BWJ5	Splicing factor 3B subunit 5	SF3B5 SF3B10	Homo sapiens (human)	0	1
P14550	Aldo-keto reductase family 1 member A1	AKR1A1 ALDR1 ALR	Homo sapiens (human)	0	1	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 Barrett's esophagus Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prinzmetal angina Reye syndrome Stargardt disease Wernicke-Korsakoff syndrome acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adrenoleukodystrophy adult fibrosarcoma age related macular degeneration alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis amnestic disorder anaplastic astrocytoma anorectal stricture arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation atrophy of testis autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome background diabetic retinopathy benign ependymoma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma brain cancer brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis cardiovascular system disease cellular ependymoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood ependymoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy dysthymic disorder embryoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential tremor exudative vitreoretinopathy familial periodic paralysis fibrillary astrocytoma fibrosarcoma gallbladder disease gastric cardia adenocarcinoma gemistocytic astrocytoma glucocorticoid-remediable aldosteronism glycogen storage disease II granular cell carcinoma granuloma annulare head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension hypopharynx cancer immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease intrahepatic cholangiocarcinoma juvenile pilocytic astrocytoma kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macular degeneration major depressive disorder malaria malignant astrocytoma marasmus melancholic depression migraine myocardial infarction myopathy myxopapillary ependymoma neurodegenerative disease neuropathy neurotic disorder nicotine dependence non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete constipation obsolete eye and adnexa disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oral candidiasis osteoporosis osteosarcoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary ependymoma papillary renal cell carcinoma perinatal necrotizing enterocolitis peripheral nervous system disease pharynx cancer pilocytic astrocytoma placental insufficiency polyneuropathy proliferative diabetic retinopathy prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma renal carcinoma renal cell carcinoma reticulosarcoma sarcomatoid renal cell carcinoma schizophrenia scurvy sensorineural hearing loss silent myocardial infarction squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tanycytic ependymoma tongue squamous cell carcinoma tracheal disease 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 urinary bladder cancer viral infectious disease vulvovaginal candidiasis
O43556	Epsilon-sarcoglycan	SGCE ESG	Homo sapiens (human)	1	5
Q14106	Protein Tob2	TOB2 KIAA1663 TOB4 TROB2	Homo sapiens (human)	1	1
Q6SJ93	Serine protease FAM111B	FAM111B CANP	Homo sapiens (human)	0	1
Q92185	Alpha-N-acetylneuraminide alpha-2,8-sialyltransferase	ST8SIA1 SIAT8 SIAT8A	Homo sapiens (human)	4	0	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 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer central nervous system cancer cerebral degeneration chronic myeloid leukemia colorectal cancer colorectal carcinoma coronary artery disease endocrine exophthalmos gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma high grade glioma invasive ductal carcinoma large intestine cancer liver disease lung benign neoplasm lung carcinoma melanoma mixed glioma multiple sclerosis neuroblastoma primary immunodeficiency disease secondary Parkinson disease skin melanoma thromboangiitis obliterans toxic encephalopathy
P25054	Adenomatous polyposis coli protein	APC DP2.5	Homo sapiens (human)	7	4
E9PJT6	Solute carrier family 43 member 3 (Fragment)	SLC43A3	Homo sapiens (human)	1	0
A0A7I2YQB3	Cathepsin F	CTSF	Homo sapiens (human)	1	0
C0M120	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
Q96LI9	Uncharacterized protein CXorf58	CXorf58	Homo sapiens (human)	2	1
K7EJY8	Galectin 3 binding protein (Fragment)	LGALS3BP	Homo sapiens (human)	2	0
Q86V42	Protein FAM124A	FAM124A	Homo sapiens (human)	1	1
Q9UKN1	Mucin-12	MUC12 MUC11	Homo sapiens (human)	22	1
Q8NAP3	Zinc finger and BTB domain-containing protein 38	ZBTB38	Homo sapiens (human)	1	1
T2HUW8	Carcinoembryonic antigen-related cell adhesion molecule 5 isoform 3D	CEACAM5	Homo sapiens (human)	1	0
P54098	DNA polymerase subunit gamma-1	POLG MDP1 POLG1 POLGA	Homo sapiens (human)	0	1
Q86VZ1	P2Y purinoceptor 8	P2RY8	Homo sapiens (human)	2	1

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