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 **15101 - 15125** of **18496** in total

« First

‹ Prev

…

601

602

603

604

605

606

607

608

609

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	Disease Ontology
K7EKX1	Protein kinase C substrate 80K-H (Fragment)	PRKCSH	Homo sapiens (human)	1
T1R378	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
H0YJ88	LDL receptor related protein 1 (Fragment)	LRP1	Homo sapiens (human)	1
Q8N4M1	Choline transporter-like protein 3	SLC44A3 CTL3	Homo sapiens (human)	5
Q9NRA2	Sialin	SLC17A5	Homo sapiens (human)	3	Alzheimer's disease Balo concentric sclerosis Crimean-Congo hemorrhagic fever Gilbert syndrome HELLP syndrome IgA glomerulonephritis Japanese encephalitis Lassa fever Parkinson's disease Plasmodium falciparum malaria Reye syndrome Stevens-Johnson syndrome Wilson disease abdominal obesity-metabolic syndrome 1 acrodermatitis acute pancreatitis adrenoleukodystrophy agammaglobulinemia agranulocytosis alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma alternating exotropia amelogenesis imperfecta type 1E amnestic disorder amyotrophic lateral sclerosis type 1 anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune hepatitis autoimmune polyendocrine syndrome bilirubin metabolic disorder cancer cardiovascular system disease cataract 2 multiple types cataract 30 cataract 32 multiple types central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease cholestasis chromosome 17p13.1 deletion syndrome chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer common cold communicating hydrocephalus congenital nystagmus congenital ptosis congestive heart failure coronary artery disease dementia dengue disease dengue hemorrhagic fever depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism disseminated intravascular coagulation dissociated nystagmus dysthymic disorder embryoma epilepsy essential hypertension essential thrombocythemia exotropia familial hyperlipidemia familial nephrotic syndrome fascioliasis fibromyalgia gallbladder disease gingival hypertrophy gingival overgrowth glomerulonephritis glucose intolerance glycogen storage disease II head and neck squamous cell carcinoma heart disease hemochromatosis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hyperglycemia hypertension hypohidrotic ectodermal dysplasia immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome intellectual disability intrahepatic cholestasis of pregnancy intrinsic asthma iron metabolism disease kidney disease kidney failure large intestine cancer late onset Parkinson's disease learning disability leukodystrophy leukopenia lipoid nephrosis lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung cancer lung non-small cell carcinoma lymphopenia lysosomal storage disease macrocytic anemia major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma microphthalmia monocular exotropia myelodysplastic syndrome myocarditis myositis narcolepsy nasopharyngitis nephritis nephrosis nephrotic syndrome neurodegenerative disease neurotic disorder neutropenia obesity obsolete Matthew-Wood syndrome obsolete melancholia obstructive hydrocephalus obstructive sleep apnea osteoarthritis osteomalacia pancreatitis pancytopenia parapsoriasis pathologic nystagmus pneumonia portal vein thrombosis pre-eclampsia prediabetes syndrome primary polycythemia primary sclerosing cholangitis psoriasis ptosis purpura fulminans pustulosis of palm and sole pyoureter retrograde amnesia rheumatoid arthritis rickets sclerosing cholangitis senile degeneration of brain severe congenital neutropenia sialuria sickle cell anemia skin melanoma spontaneous ocular nystagmus steatotic liver disease subcortical band heterotopia thrombocytopenia tuberculosis type 2 diabetes mellitus uremia viral infectious disease visceral leishmaniasis visual epilepsy yellow fever
P15248	Interleukin-9	IL9	Homo sapiens (human)	4
C8CHA8	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
A0A4P2ST97	MHC class I antigen	HLA-C	Homo sapiens (human)	1
O75871	Carcinoembryonic antigen-related cell adhesion molecule 4	CEACAM4 CGM7	Homo sapiens (human)	4
G1ENM5	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
A0A087WWD4	Neural cell adhesion molecule 1	NCAM1	Homo sapiens (human)	1
A0A804HHT8	Voltage-dependent L-type calcium channel subunit alpha (Fragment)	CACNA1C	Homo sapiens (human)	1
F5H3G7	Oxidized low-density lipoprotein receptor 1 (Fragment)	OLR1	Homo sapiens (human)	1
M9PAK0	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
M0QX44	Amino acid transporter (Fragment)	SLC1A5	Homo sapiens (human)	1
B4DNS5	cDNA FLJ54963, highly similar to Tubulointerstitial nephritis antigen-like	TINAGL1	Homo sapiens (human)	1
A0A2U9AEN5	MHC class I protein (Fragment)	HLA-C	Homo sapiens (human)	1
A0A0B7NY93	MHC class I antigen	HLA-C	Homo sapiens (human)	1
V5NQC6	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
G8ZB26	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
A0A7P0TB41	cathepsin X	CTSZ	Homo sapiens (human)	1
Q9Y6U7	RING finger protein 215	RNF215	Homo sapiens (human)	1
Q8N386	Leucine-rich repeat-containing protein 25	LRRC25 MAPA	Homo sapiens (human)	4
A0A0K0K1C4	T cell receptor beta variable 27	TRBV27	Homo sapiens (human)	1
H2BEA0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements