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 **18226 - 18250** 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
Q9BSL1	Ubiquitin-associated domain-containing protein 1	UBAC1 GBDR1 KPC2 UBADC1	Homo sapiens (human)	1	2
Q05209	Tyrosine-protein phosphatase non-receptor type 12	PTPN12	Homo sapiens (human)	15	4
Q9NTK5	Obg-like ATPase 1	OLA1 GTPBP9	Homo sapiens (human)	0	1
A0A4P2ST92	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
A0A7I2V6B0	NODAL modulator 3	NOMO3	Homo sapiens (human)	1	0
Q9UBV2	Protein sel-1 homolog 1	SEL1L TSA305	Homo sapiens (human)	14	47
E7EMM4	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
A0A2X0SR84	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
A3KFI2	NBL1, DAN family BMP antagonist (Fragment)	NBL1	Homo sapiens (human)	1	0
Q8TDV2	Probable G-protein coupled receptor 148	GPR148 BTR PGR6	Homo sapiens (human)	1	0
Q96QD8	Sodium-coupled neutral amino acid symporter 2	SLC38A2 ATA2 KIAA1382 SAT2 SNAT2	Homo sapiens (human)	2	1
P49448	Glutamate dehydrogenase 2, mitochondrial	GLUD2 GLUDP1	Homo sapiens (human)	2	2
P38484	Interferon gamma receptor 2	IFNGR2 IFNGT1	Homo sapiens (human)	6	3
Q9Y446	Plakophilin-3	PKP3	Homo sapiens (human)	0	1
Q6PRD1	Probable G-protein coupled receptor 179	GPR179 GPR158L GPR158L1	Homo sapiens (human)	3	1
P41222	Prostaglandin-H2 D-isomerase	PTGDS PDS	Homo sapiens (human)	8	223	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 Axenfeld-Rieger syndrome Crohn's colitis Crohn's disease Fabry disease Graves' disease Guillain-Barre syndrome Loeffler syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome Parkinson's disease Pendred Syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acrodermatitis acute myocardial infarction acute promyelocytic leukemia adult lymphoma adult medulloblastoma allergic asthma alopecia anaplastic astrocytoma androgenic alopecia angiomatous meningioma aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atopic dermatitis attention deficit hyperactivity disorder autoimmune thyroiditis benign meningioma bipolar disorder brain cancer breast cancer breast carcinoma bronchiolitis bronchitis cancer carcinoma cardiovascular system disease carotid artery disease central nervous system lymphoma cerebral convexity meningioma cerebral degeneration cerebrotendinous xanthomatosis childhood cerebral astrocytoma childhood lymphoma childhood medulloblastoma cholestasis chronic ethmoiditis chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis craniosynostosis cryptorchidism depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma disease of mental health dry eye syndrome dyshormonogenic goiter dysthymic disorder egg allergy embryoma encephalitis encephalomyelitis enterocele eosinophilic pneumonia essential hypertension fibrillary astrocytoma fibrous meningioma gastritis gastroenteritis gemistocytic astrocytoma giant cell glioblastoma glioblastoma glomerulonephritis goiter heart disease high grade glioma hypereosinophilic syndrome hyperglycemia hyperinsulinism hypertension hyperthyroidism hypertrichosis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer intraorbital meningioma intraventricular meningioma intrinsic asthma juvenile pilocytic astrocytoma kidney disease large congenital melanocytic nevus large intestine cancer late onset Parkinson's disease lipid storage disease liver cirrhosis lung benign neoplasm lupus nephritis lymphoma lymphoplasmacyte-rich meningioma major depressive disorder malignant astrocytoma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningioma meningothelial meningioma microcystic meningioma myelitis myocardial infarction nephritis nephrosis neurofibromatosis neurotic disorder nontoxic goiter nutmeg liver obesity obsolete dyspepsia obsolete melancholia obsolete ymphosarcoma obstructive sleep apnea olfactory groove meningioma open-angle glaucoma osteoarthritis ovarian cancer ovarian carcinoma pancytopenia papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma periodontitis pigment dispersion syndrome pilocytic astrocytoma pituitary adenoma pneumonia post-traumatic stress disorder pre-eclampsia prostate cancer prostate carcinoma protoplasmic astrocytoma psammomatous meningioma psychotic disorder pyoureter respiratory syncytial virus infectious disease rhinitis sarcomatoid carcinoma schizophrenia secretory meningioma sensorineural hearing loss silent myocardial infarction sinusitis situs inversus skin melanoma skin squamous cell carcinoma spinal meningioma squamous cell carcinoma stomach cancer stomach carcinoma stuttering subependymal giant cell astrocytoma systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transitional meningioma tuberous sclerosis type 2 diabetes mellitus ulcerative colitis ureteral obstruction vestibular schwannomatosis xerophthalmia
O95528	Solute carrier family 2, facilitated glucose transporter member 10	SLC2A10 GLUT10	Homo sapiens (human)	1	0	Hailey-Hailey disease Legg-Calve-Perthes disease Loeys-Dietz syndrome Moyamoya disease Rothmund-Thomson syndrome X-linked dilated cardiomyopathy acute myocardial infarction adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma aortic aneurysm aortic valve disease 2 aortic valve insufficiency aortic valve stenosis arterial tortuosity syndrome asthma 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 blepharophimosis bone disease breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiomyopathy cartilage disease cataract 32 multiple types cerebral infarction cerebrovascular disease childhood type dermatomyositis chondrosarcoma collagen disease congenital central hypoventilation syndrome congenital diaphragmatic hernia congestive heart failure connective tissue disease corneal disease coronary thrombosis craniosynostosis cribriform carcinoma cutis laxa dermatomyositis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy endomyocardial fibrosis esophagitis essential hypertension familial hypertrophic cardiomyopathy gastroesophageal reflux disease granular cell carcinoma hiatus hernia hypertension hypertrophic cardiomyopathy hypertropia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inguinal hernia intellectual disability intermittent claudication interstitial lung disease intrinsic asthma keratoconus learning disability leukocyte adhesion deficiency 1 leukocyte adhesion deficiency lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma mal de Meleda mechanical strabismus megalocornea myocardial infarction myocarditis myopia newborn respiratory distress syndrome obstructive lung disease omphalocele ophthalmoplegia peptic esophagitis peripheral artery disease peripheral vascular disease pneumonia pulmonary emphysema pyloric stenosis respiratory failure restrictive dermopathy scoliosis silent myocardial infarction strabismus thoracic aortic aneurysm tubular adenocarcinoma type 2 diabetes mellitus umbilical hernia vascular disease
E3Q0Y1	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q08345	Epithelial discoidin domain-containing receptor 1	DDR1 CAK EDDR1 NEP NTRK4 PTK3A RTK6 TRKE	Homo sapiens (human)	6	1
O14514	Adhesion G protein-coupled receptor B1	ADGRB1 BAI1	Homo sapiens (human)	7	3
Q6MZP7	Protein lin-54 homolog	LIN54 CXCDC1 KIAA2037	Homo sapiens (human)	40	2
Q15415	RNA-binding motif protein, Y chromosome, family 1 member F/J	RBMY1F RBMY1J YRRM2	Homo sapiens (human)	1	1
Q9BVA1	Tubulin beta-2B chain	TUBB2B	Homo sapiens (human)	1	1
A0A5F9ZHF5	Biotinidase	BTD	Homo sapiens (human)	1	0
Q8NBH2	Kyphoscoliosis peptidase	KY	Homo sapiens (human)	0	1

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