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 **17276 - 17300** 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
Q93052	Lipoma-preferred partner	LPP	Homo sapiens (human)	15	5
Q9BU40	Chordin-like protein 1	CHRDL1 NRLN1	Homo sapiens (human)	5	5
Q96D42	Hepatitis A virus cellular receptor 1	HAVCR1 KIM1 TIM1 TIMD1	Homo sapiens (human)	5	5
P20023	Complement receptor type 2	CR2 C3DR	Homo sapiens (human)	13	5
P26842	CD27 antigen	CD27 TNFRSF7	Homo sapiens (human)	4	5
Q16555	Dihydropyrimidinase-related protein 2	DPYSL2 CRMP2 ULIP2	Homo sapiens (human)	11	5
P23327	Sarcoplasmic reticulum histidine-rich calcium-binding protein	HRC HCP	Homo sapiens (human)	3	5
P36980	Complement factor H-related protein 2	CFHR2 CFHL2 FHR2 HFL3	Homo sapiens (human)	1	5
P27448	MAP/microtubule affinity-regulating kinase 3	MARK3 CTAK1 EMK2	Homo sapiens (human)	3	5
Q86Z14	Beta-klotho	KLB	Homo sapiens (human)	13	5	Clostridium difficile colitis allergic rhinitis autosomal dominant hypophosphatemic rickets breast cancer breast carcinoma cancer cartilage-hair hypoplasia diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism embryoma familial hyperlipidemia gestational diabetes hepatocellular carcinoma intrahepatic cholestasis of pregnancy invasive ductal carcinoma irritable bowel syndrome kidney failure liver cancer lung cancer lung non-small cell carcinoma neurocirculatory asthenia nodular prostate obesity ovarian disease papillary adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma prostatic adenoma steatotic liver disease thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma type 2 diabetes mellitus uremia vasomotor rhinitis
O75970	Multiple PDZ domain protein	MPDZ MUPP1	Homo sapiens (human)	2	5
Q9NRA1	Platelet-derived growth factor C	PDGFC SCDGF	Homo sapiens (human)	3	5
P27824	Calnexin	CANX	Homo sapiens (human)	11	5	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Lyme disease MASA syndrome Marfan syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 absence epilepsy acute myocardial infarction adult medulloblastoma agenesis of the corpus callosum with peripheral neuropathy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system lymphoma cervical squamous cell carcinoma cervix uteri carcinoma in situ childhood absence epilepsy childhood medulloblastoma childhood osteosarcoma cone-rod dystrophy coronary artery disease coronary thrombosis diabetes mellitus diabetic angiopathy diabetic ketoacidosis embryoma exanthema subitum fundus albipunctatus giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperinsulinism interstitial lung disease keratosis follicularis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma mongolian spot monoclonal gammopathy of uncertain significance motor peripheral neuropathy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple myeloma multiple sclerosis myocardial infarction nephrogenic diabetes insipidus neuropathy nodular prostate obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum oculocutaneous albinism type IA oculocutaneous albinism osteosarcoma peripheral nervous system disease platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 polyneuropathy post-traumatic stress disorder progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pseudoachondroplasia pseudoxanthoma elasticum renal tubular acidosis retinitis pigmentosa rubella silent myocardial infarction situs inversus skin melanoma spinal muscular atrophy stomach cancer stomach carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus vitiligo von Willebrand's disease
O75376	Nuclear receptor corepressor 1	NCOR1 KIAA1047	Homo sapiens (human)	82	5
Q86WI1	Fibrocystin-L	PKHD1L1	Homo sapiens (human)	10	6
Q8WZ75	Roundabout homolog 4	ROBO4	Homo sapiens (human)	6	6
Q6UWW8	Carboxylesterase 3	CES3	Homo sapiens (human)	2	6
Q7Z4F1	Low-density lipoprotein receptor-related protein 10	LRP10	Homo sapiens (human)	4	6
P28845	11-beta-hydroxysteroid dehydrogenase 1	HSD11B1 HSD11 HSD11L SDR26C1	Homo sapiens (human)	3	6	ACTH-secreting pituitary adenoma Addison's disease 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 Clostridium difficile colitis Norum disease Pick's disease Reye syndrome Tangier disease Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acidophil adenoma acromegaly actinic keratosis acute myocardial infarction adamantinous craniopharyngioma adenocarcinoma adenoma adrenal cortical hypofunction adrenal gland cancer adrenal gland hyperfunction adrenoleukodystrophy age related macular degeneration allergic contact dermatitis alopecia amnestic disorder amyloidosis apparent mineralocorticoid excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis atrial fibrillation bone osteosarcoma breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma cancer cardiovascular system disease cerebellar ataxia, mental retardation and dysequlibrium syndrome cerebral degeneration cerebrotendinous xanthomatosis childhood osteosarcoma choreaacanthocytosis chronic ethmoiditis chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis colorectal cancer colorectal carcinoma cone-rod dystrophy 2 cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis cortisone reductase deficiency 2 cortisone reductase deficiency craniopharyngioma craniosynostosis cribriform carcinoma degeneration of macula and posterior pole dementia depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism dissociative amnesia dysthymic disorder embryoma essential hypertension familial hyperlipidemia fibromyalgia follicular adenoma functionless pituitary adenoma gallbladder disease gastrointestinal stromal tumor gestational diabetes glaucoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma hyperandrogenism hyperglycemia hyperhomocysteinemia hyperinsulinism hyperpituitarism hypertension hypolipoproteinemia inflammatory bowel disease irritable bowel syndrome large intestine cancer liver cancer liver disease lung cancer macular degeneration major depressive disorder malaria melancholic depression melanoma microcystic adenoma myocardial infarction myositis neurocirculatory asthenia neurotic disorder nutmeg liver obesity obsolete Cushing's syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoarthritis osteoporosis osteosarcoma papillary adenoma papillary craniopharyngioma pituitary-dependent Cushing's disease pleural tuberculosis pneumonia polycystic ovary syndrome postpartum depression pre-eclampsia prediabetes syndrome primary hyperaldosteronism prostate cancer prostate carcinoma psychotic disorder pulmonary tuberculosis retrograde amnesia rheumatoid arthritis seborrheic keratosis silent myocardial infarction skin benign neoplasm skin cancer skin disease skin melanoma status epilepticus steatotic liver disease synovitis systemic lupus erythematosus tenosynovitis tuberculous pneumothorax 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
Q9UQV4	Lysosome-associated membrane glycoprotein 3	LAMP3 DCLAMP TSC403	Homo sapiens (human)	9	6
Q8IUK5	Plexin domain-containing protein 1	PLXDC1 TEM3 TEM7	Homo sapiens (human)	6	6
P30542	Adenosine receptor A1	ADORA1	Homo sapiens (human)	1	6
P08238	Heat shock protein HSP 90-beta	HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB	Homo sapiens (human)	6	6
Q9BWV1	Brother of CDO	BOC	Homo sapiens (human)	10	6
P22695	Cytochrome b-c1 complex subunit 2, mitochondrial	UQCRC2	Homo sapiens (human)	3	6

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