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 **2801 - 2825** of **18496** in total

« First

‹ Prev

…

109

110

111

112

113

114

115

116

117

…

Next ›

Last »
UniProt ID ▲	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
B0FWH6	Sex hormone-binding globulin (Fragment)	SHBG	Homo sapiens (human)	2	0
B0FYL6	MICA protein (Fragment)	MICA	Homo sapiens (human)	3	0
B0FYL7	MICA protein (Fragment)	MICA	Homo sapiens (human)	3	0
B0FZC9	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
B0FZD0	MHC class I polypeptide-related sequence A (Fragment)	MICA	Homo sapiens (human)	3	0
B0I1T2	Unconventional myosin-Ig	MYO1G HA2	Homo sapiens (human)	1	1
B0JF23	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
B0L3P6	Lactosylceramide 4-alpha-galactosyltransferase	A4GALT	Homo sapiens (human)	1	0
B0L3P7	Lactosylceramide 4-alpha-galactosyltransferase	A4GALT	Homo sapiens (human)	1	0
B0YJ32	Laminin alpha-3 chain variant 1	LAMA3	Homo sapiens (human)	3	0
B0YJ81	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1	HACD1 PTPLA	Homo sapiens (human)	1	0	B-cell lymphoma Ehrlich tumor carcinoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Lyme disease Perry syndrome Streptococcus pneumonia T-cell acute lymphoblastic leukemia X-linked dilated cardiomyopathy achondroplasia acute biphenotypic leukemia acute leukemia agnosia allergic asthma allergic rhinitis androgen insensitivity syndrome anthrax disease aplastic anemia arrhythmogenic right ventricular cardiomyopathy asthma autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy beta thalassemia bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma cancer centronuclear myopathy cerebral infarction cerebrovascular disease cervix uteri carcinoma in situ childhood osteosarcoma clubfoot colitis common cold congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital myopathy 4A congenital ptosis congenital structural myopathy cryptococcosis cryptorchidism developmental coordination disorder 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 distal myopathy embryoma epilepsy facioscapulohumeral muscular dystrophy gastroenteritis giant cell glioblastoma glioblastoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma ileitis ileocolitis influenza intellectual disability intrinsic asthma learning disability limb-girdle muscular dystrophy liver cancer liver cirrhosis mantle cell lymphoma megaconial type congenital muscular dystrophy multidrug-resistant tuberculosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy nemaline myopathy obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete ymphosarcoma oculopharyngeal muscular dystrophy ophthalmoplegia osteosarcoma ovarian cancer ovarian carcinoma paroxysmal nocturnal hemoglobinuria pleural empyema pneumonia polycystic ovary syndrome polyhydramnios premature menopause primary ovarian insufficiency prostate cancer prostate carcinoma ptosis recurrent hypersomnia rigid spine muscular dystrophy 1 scoliosis sick sinus syndrome steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder thalassemia thymic carcinoma thymoma tuberculosis type 2 diabetes mellitus type C thymoma vasomotor rhinitis viral infectious disease wheat allergy
B0ZBE2	Angiotensinogen	AGT hFLT1	Homo sapiens (human)	2	0
B1A0K3	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
B1AA54	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
B1AHL2	Fibulin-1	FBLN1	Homo sapiens (human)	3	0
B1AHM6	Fibulin 1 (Fragment)	FBLN1	Homo sapiens (human)	1	0
B1AHM7	Fibulin 1 (Fragment)	FBLN1	Homo sapiens (human)	1	0
B1AHM8	Fibulin 1 (Fragment)	FBLN1	Homo sapiens (human)	1	0
B1AHM9	Fibulin 1 (Fragment)	FBLN1	Homo sapiens (human)	1	0
B1AHN3	Fibulin 1 (Fragment)	FBLN1	Homo sapiens (human)	1	0
B1AJZ9	Forkhead-associated domain-containing protein 1	FHAD1 KIAA1937	Homo sapiens (human)	4	1
B1AKC9	receptor protein-tyrosine kinase	EPHB2	Homo sapiens (human)	1	0
B1AKG0	Complement factor H related 1	CFHR1	Homo sapiens (human)	1	0
B1AKI9	Isthmin-1	ISM1 C20orf82 ISM	Homo sapiens (human)	1	0
B1AL88	NALCN channel auxiliary factor 1	NALF1 FAM155A NLF-1	Homo sapiens (human)	1	0

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements