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 **976 - 1000** 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
P05451	Lithostathine-1-alpha	REG1A PSPS PSPS1 REG	Homo sapiens (human)	1	0
O15405	TOX high mobility group box family member 3	TOX3 CAGF9 TNRC9	Homo sapiens (human)	2	1
F2X624	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q96ET8	Golgi apparatus membrane protein TVP23 homolog C	TVP23C FAM18B2	Homo sapiens (human)	1	1
G3D6C9	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8IX12	Cell division cycle and apoptosis regulator protein 1	CCAR1 CARP1 DIS	Homo sapiens (human)	30	3
Q9UM73	ALK tyrosine kinase receptor	ALK	Homo sapiens (human)	16	1
A0A5H2UF49	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
P06280	Alpha-galactosidase A	GLA	Homo sapiens (human)	3	44	Fabry disease Gaucher's disease Goodpasture syndrome Horner's syndrome Laron syndrome Meckel syndrome Moyamoya disease Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Riley-Day syndrome Takayasu's arteritis X-linked agammaglobulinemia Zollinger-Ellison syndrome achondroplasia acquired hyperkeratosis acute myocardial infarction allergic asthma anemia angiokeratoma anhidrosis antithrombin III deficiency anxiety disorder arthritis arthropathy asthma atrial fibrillation atrioventricular block autosomal dominant polycystic kidney disease bacterial vaginosis breast cancer breast fibrocystic disease brucellosis cancer cardiomyopathy cardiovascular system disease cataract central nervous system origin vertigo cerebral infarction cerebrovascular disease chronic kidney disease chronic obstructive pulmonary disease chylomicron retention disease congenital hypogammaglobulinemia congestive heart failure corneal dystrophy coronary thrombosis cystinuria depressive disorder diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism dysthymic disorder elephantiasis endomyocardial fibrosis epilepsy erythromelalgia essential hypertension familial hyperlipidemia familial hypertrophic cardiomyopathy familial mediterranean fever familial nephrotic syndrome fibromyalgia galactosemia generalized anxiety disorder glaucoma glomerulonephritis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease granulomatosis with polyangiitis heart disease hyperinsulinism hypertension hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy hypoglycemia hypohidrosis influenza inherited metabolic disorder interstitial nephritis intrinsic asthma keratosis follicularis kidney disease kidney failure late onset Parkinson's disease lipid storage disease lipoid nephrosis lung disease lymphedema lysosomal storage disease macrocytic anemia major depressive disorder melancholic depression mevalonic aciduria microglandular adenosis mitral valve insufficiency mitral valve prolapse mongolian spot multiple sclerosis myocardial infarction myositis nephritis nephrosis nephrotic syndrome neurohypophyseal diabetes insipidus neuropathy neurotic disorder obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive lung disease optic atrophy osteoarthritis papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease pneumonia polyarteritis nodosa polyneuropathy priapism protein C deficiency protein S deficiency proteinuria pseudoxanthoma elasticum pyelitis pyelonephritis pyoureter recurrent corneal erosion renal infectious disease sensorineural hearing loss sick sinus syndrome silent myocardial infarction sphingolipidosis thrombophilia thyroid gland papillary carcinoma transient cerebral ischemia tuberculosis 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 uremia vaginitis vascular disease vertebrobasilar insufficiency visual epilepsy vitamin K deficiency bleeding vulvitis vulvovaginal candidiasis vulvovaginitis
Q9UGM3	Deleted in malignant brain tumors 1 protein	DMBT1 GP340	Homo sapiens (human)	26	1
Q8N9H8	Exonuclease mut-7 homolog	EXD3	Homo sapiens (human)	0	1
Q9BUD6	Spondin-2	SPON2 DIL1	Homo sapiens (human)	2	1
Q8WXH0	Nesprin-2	SYNE2 KIAA1011 NUA	Homo sapiens (human)	9	5
Q86YH6	All trans-polyprenyl-diphosphate synthase PDSS2	PDSS2 C6orf210 DLP1	Homo sapiens (human)	0	1
Q6PEJ8	HP protein	HP	Homo sapiens (human)	4	0
Q9GZY8	Mitochondrial fission factor	MFF C2orf33	Homo sapiens (human)	4	1
Q14093	Cylicin-2	CYLC2 CYL2	Homo sapiens (human)	1	1
Q96SK3	Zinc finger protein 607	ZNF607	Homo sapiens (human)	0	1
P62136	Serine/threonine-protein phosphatase PP1-alpha catalytic subunit	PPP1CA PPP1A	Homo sapiens (human)	0	1
Q4VNC0	Probable cation-transporting ATPase 13A5	ATP13A5	Homo sapiens (human)	3	0
Q68DA7	Formin-1	FMN1 FMN LD	Homo sapiens (human)	1	2
A0A1S5QR77	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P32322	Pyrroline-5-carboxylate reductase 1, mitochondrial	PYCR1	Homo sapiens (human)	4	1
P23582	C-type natriuretic peptide	NPPC CNP2	Homo sapiens (human)	1	1
Q8NFP0	Peroxisomal testis-specific protein 1	PXT1 STEPP	Homo sapiens (human)	0	1

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