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 **16276 - 16300** 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
Q53GD3	Choline transporter-like protein 4	SLC44A4 C6orf29 CTL4 NG22 TPPT1	Homo sapiens (human)	7	10
Q8N4M1	Choline transporter-like protein 3	SLC44A3 CTL3	Homo sapiens (human)	5	0
Q8IWA5	Choline transporter-like protein 2	SLC44A2 CTL2	Homo sapiens (human)	4	24
Q8WWI5	Choline transporter-like protein 1	SLC44A1 CD92 CDW92 CTL1	Homo sapiens (human)	3	15
A0A024R798	Choline transporter-like protein	SLC44A2	Homo sapiens (human)	2	0
A0A088QF11	Choline transporter-like protein	SLC44A2	Homo sapiens (human)	2	0
A0A088QCU6	Choline transporter-like protein	SLC44A2	Homo sapiens (human)	2	0
P28329	Choline O-acetyltransferase	CHAT	Homo sapiens (human)	3	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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Balo concentric sclerosis Down syndrome Gilles de la Tourette syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lambert-Eaton myasthenic syndrome Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Rett syndrome Reye syndrome X-linked adrenal hypoplasia congenita acute myocardial infarction adrenoleukodystrophy agnosia allergic asthma amnestic disorder amyloidosis angle-closure glaucoma arthritis arthropathy aspiration pneumonia aspiration pneumonitis asthma atrial fibrillation autism spectrum disorder autistic disorder beriberi bronchus cancer bronchus carcinoma bulbar polio cancer cannabis abuse cannabis dependence central nervous system disease central sleep apnea centronuclear myopathy cerebral degeneration cerebral infarction cerebrovascular disease chronic closed-angle glaucoma chronic fatigue syndrome clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital myasthenic syndrome 21 congenital myasthenic syndrome 6 congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy coronary thrombosis critical illness polyneuropathy dementia depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis differentiating neuroblastoma disease of mental health dissociated nystagmus dry beriberi dysthymic disorder encephalitis encephalomyelitis epilepsy esophagitis esotropia focal epilepsy gastroesophageal reflux disease gastroparesis giant cell glioblastoma glioblastoma hypertropia hypoglycemia idiopathic interstitial pneumonia intellectual disability intrinsic asthma kernicterus due to isoimmunization kernicterus lactic acidosis large intestine cancer learning disability lung benign neoplasm lung cancer lung carcinoma lymphocytic choriomeningitis major depressive disorder mechanical strabismus melancholic depression middle cerebral artery infarction monocular esotropia mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple sclerosis myelitis myocardial infarction narcolepsy nervous system disease neuroblastoma neurodegenerative disease neuromuscular disease neurotic disorder nicotine dependence obsolete constipation obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea olivopontocerebellar atrophy ophthalmoplegia osteoarthritis partial motor epilepsy pathologic nystagmus pellagra peptic esophagitis poliomyelitis polyhydramnios polyneuropathy postinflammatory pulmonary fibrosis primary angle-closure glaucoma progressive bulbar palsy psychotic disorder ptosis pulmonary fibrosis red-green color blindness retinal disease retinitis retrograde amnesia rheumatoid arthritis schizophrenia scoliosis secondary Parkinson disease sensorineural hearing loss silent myocardial infarction situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus sudden infant death syndrome tendinitis thiamine deficiency disease tuberous sclerosis 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 vascular dementia visual epilepsy
A0A0S2Z3F6	Cholesteryl ester transfer protein (Fragment)	CETP	Homo sapiens (human)	1	0
H3BRJ9	Cholesteryl ester transfer protein	CETP	Homo sapiens (human)	1	0
P11597	Cholesteryl ester transfer protein	CETP	Homo sapiens (human)	5	15
Q8WWZ7	Cholesterol transporter ABCA5	ABCA5 KIAA1888	Homo sapiens (human)	3	0
O95992	Cholesterol 25-hydroxylase	CH25H	Homo sapiens (human)	3	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 Balo concentric sclerosis Marfan syndrome Pick's disease Reye syndrome Zika fever adrenoleukodystrophy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis bacterial infectious disease central nervous system disease cerebral degeneration childhood leukemia chronic fatigue syndrome chronic obstructive pulmonary disease colitis coronary artery disease encephalitis encephalomyelitis familial hypercholesterolemia gastroenteritis giant cell glioblastoma glioblastoma hepatitis C high grade glioma ileitis ileocolitis leukemia melanoma microcephaly multiple sclerosis myelitis narcolepsy nervous system disease neuromyelitis optica osteoarthritis plasmacytoma polycythemia vera polycythemia pulmonary emphysema rabies situs inversus skin melanoma tuberous sclerosis type 2 diabetes mellitus
Q9Y6A2	Cholesterol 24-hydroxylase	CYP46A1 CYP46	Homo sapiens (human)	2	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 Creutzfeldt-Jakob disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lennox-Gastaut syndrome Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 age related macular degeneration amyloidosis brain disease cancer cardiac arrest cerebral degeneration cerebrovascular disease chronic fatigue syndrome colorectal cancer colorectal carcinoma degeneration of macula and posterior pole depressive disorder diabetes mellitus dysthymic disorder encephalitis encephalomyelitis giant cell glioblastoma glioblastoma high grade glioma large intestine cancer macular degeneration major depressive disorder melancholic depression multiple sclerosis myelitis neurodegenerative disease neurotic disorder obsolete melancholia primary open angle glaucoma tauopathy type 2 diabetes mellitus
P32238	Cholecystokinin receptor type A	CCKAR CCKRA	Homo sapiens (human)	3	0
P06307	Cholecystokinin	CCK	Homo sapiens (human)	1	0
Q9Y696	Chloride intracellular channel protein 4	CLIC4	Homo sapiens (human)	0	1
O15247	Chloride intracellular channel protein 2	CLIC2	Homo sapiens (human)	0	1
O00299	Chloride intracellular channel protein 1	CLIC1 G6 NCC27	Homo sapiens (human)	3	2
P51801	Chloride channel protein ClC-Kb	CLCNKB	Homo sapiens (human)	1	0
P51788	Chloride channel protein 2	CLCN2	Homo sapiens (human)	1	1
Q96S66	Chloride channel CLIC-like protein 1	CLCC1 KIAA0761 MCLC	Homo sapiens (human)	7	1
P40879	Chloride anion exchanger	SLC26A3 DRA	Homo sapiens (human)	3	0
Q13231	Chitotriosidase-1	CHIT1	Homo sapiens (human)	2	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 Bloch-Sulzberger syndrome Creutzfeldt-Jakob disease Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Krabbe disease Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Wolman disease acute myeloid leukemia adrenoleukodystrophy alkaptonuria allergic asthma allergic rhinitis amyloidosis amyotrophic lateral sclerosis ancylostomiasis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascariasis ascaridiasis aspartylglucosaminuria asthma atherosclerosis bacterial sepsis beta thalassemia bone marrow cancer breast cancer breast carcinoma cancer carotid artery thrombosis carotid stenosis cerebral degeneration cerebral infarction cerebrovascular disease childhood type dermatomyositis cholestasis chronic obstructive pulmonary disease chylomicron retention disease colorectal cancer colorectal carcinoma common variable immunodeficiency complement deficiency coronary artery disease cryptococcosis cystic fibrosis dementia dermatomyositis diabetes mellitus diabetic ketoacidosis embryoma essential thrombocythemia eumycotic mycetoma familial combined hyperlipidemia familial mediterranean fever filariasis follicular lymphoma frontotemporal dementia fucosidosis gastritis glomerulonephritis glycoproteinosis hepatitis C hypomelanosis of Ito idiopathic interstitial pneumonia interstitial lung disease intrinsic asthma juvenile rheumatoid arthritis kidney disease large intestine cancer lipid storage disease liver cirrhosis lung disease lysosomal acid lipase deficiency lysosomal storage disease malaria mevalonic aciduria multiple sclerosis myelofibrosis myeloproliferative neoplasm nephritis nephrosis neurodegenerative disease neuropathy nodal marginal zone lymphoma nutmeg liver obesity obstructive sleep apnea ochronosis osteoarthritis peripheral nervous system disease plasmacytoma polycythemia vera polycythemia polyneuropathy postinflammatory pulmonary fibrosis progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pulmonary fibrosis pyoureter sarcoidosis sialuria sickle cell anemia sphingolipidosis steatotic liver disease thalassemia tuberculosis type 2 diabetes mellitus uveoparotid fever vascular dementia vasomotor rhinitis
Q9BT22	Chitobiosyldiphosphodolichol beta-mannosyltransferase	ALG1 HMAT1 HMT1	Homo sapiens (human)	0	1	B-cell lymphoma Cauda equina syndrome Creutzfeldt-Jakob disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Walker-Warburg syndrome amyotrophic lateral sclerosis type 1 breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cerebral degeneration cerebral infarction cerebrovascular disease colon cancer colonic benign neoplasm congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 diabetes mellitus endomyocardial fibrosis enophthalmos epilepsy familial hypertrophic cardiomyopathy familial nephrotic syndrome focal epilepsy glomerulonephritis goiter hepatocellular carcinoma hyperthyroidism hypertrophic cardiomyopathy hypogonadism kidney disease laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoma malignant pleural mesothelioma microcephaly nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome neurogenic bladder nodular goiter obsolete exophthalmos obsolete ymphosarcoma orbital disease partial motor epilepsy placental insufficiency pyoureter reticulosarcoma schizophrenia scoliosis systemic lupus erythematosus thyroid gland disease thyrotoxicosis type 2 diabetes mellitus urinary tract obstruction visual epilepsy

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