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 **13351 - 13375** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	Disease Ontology
P52849	Bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 2	NDST2 HSST2	Homo sapiens (human)	6	prostate cancer prostate carcinoma
I6M569	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
D5FZQ0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
Q1EHB4	Sodium-coupled monocarboxylate transporter 2	SLC5A12 SMCT2	Homo sapiens (human)	1
G1FTT7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
A0A078BCJ0	Transforming growth factor, beta 1 (Fragment)	TGFB1	Homo sapiens (human)	1
A0A1B1UUG9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
Q5VV63	Attractin-like protein 1	ATRNL1 KIAA0534	Homo sapiens (human)	8	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 B-cell lymphoma Becker muscular dystrophy Bloom syndrome Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Langerhans-cell histiocytosis Laron syndrome Marfan syndrome Pick's disease Reye syndrome Sjogren's syndrome Wilson disease achondroplasia acromegaly acute myeloid leukemia adult hypophosphatasia allergic asthma amyotrophic lateral sclerosis ankylosing spondylitis 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 bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer cardiovascular system disease cartilage disease cerebral degeneration cerebral palsy childhood osteosarcoma cholestasis choriocarcinoma chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer connective tissue disease craniosynostosis diabetes mellitus distal arthrogryposis distal myopathy embryonal cancer endomyocardial fibrosis esophagitis extrahepatic cholestasis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hyperlipidemia familial hypocalciuric hypercalcemia 1 gallbladder disease gastroesophageal reflux disease germ cell and embryonal cancer germ cell cancer germinoma goiter heart disease hematopoietic system disease hemiplegia hemochromatosis hepatitis C hepatitis hepatocellular carcinoma hereditary elliptocytosis hypercalcemia hyperpituitarism hypogonadism hypophosphatasia infantile hypophosphatasia inflammatory liposarcoma iron metabolism disease isolated cleft palate keratoconjunctivitis sicca kidney failure large intestine cancer limb-girdle muscular dystrophy lipoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma muscular dystrophy myeloproliferative disorder with eosinophilia myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nephrocalcinosis nephrolithiasis neurodegenerative disease non-Hodgkin lymphoma nonpapillary renal cell carcinoma nontoxic goiter 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 constipation obsolete ymphosarcoma oculopharyngeal muscular dystrophy osteoporosis osteosarcoma papillary renal cell carcinoma peptic esophagitis phosphorus metabolism disease placenta cancer pleomorphic lipoma primary biliary cholangitis primary hyperparathyroidism progressive muscular atrophy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis sarcomatoid renal cell carcinoma sclerosing liposarcoma situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy steatotic liver disease subcortical band heterotopia thyroid gland disease tuberous sclerosis type 2 diabetes mellitus uremia uric acid nephrolithiasis vitelliform macular dystrophy well-differentiated liposarcoma
D3U468	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
X5DNF2	Cell adhesion molecule 1 isoform A (Fragment)	CADM1	Homo sapiens (human)	3
R9QZR6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
G0ZMK8	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
A0A6B7FU54	MHC class I antigen	HLA-C	Homo sapiens (human)	1
G1EPS6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
P22459	Potassium voltage-gated channel subfamily A member 4	KCNA4 KCNA4L	Homo sapiens (human)	1
A0A804HJR1	Voltage-dependent L-type calcium channel subunit alpha	CACNA1C	Homo sapiens (human)	1
U4N162	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
D4HPK3	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
A0A0K0KS00	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
A0A5H2UVV9	MHC class I antigen	HLA-C	Homo sapiens (human)	1
D5FZL9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
A0A0A7C500	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
Q12918	Killer cell lectin-like receptor subfamily B member 1	KLRB1 CLEC5B NKRP1A	Homo sapiens (human)	1	Goodpasture syndrome Takayasu's arteritis acquired immunodeficiency syndrome acute promyelocytic leukemia aggressive NK-cell leukemia allergic asthma arthritis arthropathy asthma autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bone disease bronchus cancer bronchus carcinoma cancer cartilage disease cataract connective tissue disease eclampsia embryoma familial multiple nevi flammei granulomatosis with polyangiitis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hidradenitis suppurativa hidradenitis human immunodeficiency virus infectious disease immune system disease influenza intermittent claudication intrinsic asthma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 melanoma mitral valve stenosis multiple myeloma multiple sclerosis myocarditis osteoarthritis peeling skin syndrome periodontitis placental insufficiency pneumonia polyarteritis nodosa pompholyx prostate cancer prostate carcinoma psoriatic arthritis rheumatoid arthritis scleroderma skin melanoma spondyloarthropathy spondylosis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tuberculosis urinary bladder cancer viral infectious disease
Q8NE26	ADAM metallopeptidase with thrombospondin type 1 motif, 1	ADAMTS1	Homo sapiens (human)	3
G1EPJ5	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1

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