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 **851 - 875** 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
P28799	Progranulin	GRN	Homo sapiens (human)	10	31
P51805	Plexin-A3	PLXNA3 PLXN4 SEX	Homo sapiens (human)	10	2
P14616	Insulin receptor-related protein	INSRR IRR	Homo sapiens (human)	10	0
Q96K78	Adhesion G-protein coupled receptor G7	ADGRG7 GPR128	Homo sapiens (human)	10	1
Q96FE5	Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1	LINGO1 LERN1 LRRN6A	Homo sapiens (human)	10	3
P69905	Hemoglobin subunit alpha	HBA1 HBA2	Homo sapiens (human)	10	1
P00740	Coagulation factor IX	F9	Homo sapiens (human)	10	41
P26599	Polypyrimidine tract-binding protein 1	PTBP1 PTB	Homo sapiens (human)	10	2
O14522	Receptor-type tyrosine-protein phosphatase T	PTPRT KIAA0283	Homo sapiens (human)	10	0
Q01196	Runt-related transcription factor 1	RUNX1 AML1 CBFA2	Homo sapiens (human)	10	2
Q8NDC0	MAPK-interacting and spindle-stabilizing protein-like	MAPK1IP1L C14orf32	Homo sapiens (human)	10	2
Q6QNK2	Adhesion G-protein coupled receptor D1	ADGRD1 GPR133 PGR25	Homo sapiens (human)	10	12
Q9NRM1	Enamelin	ENAM	Homo sapiens (human)	10	0
Q13003	Glutamate receptor ionotropic, kainate 3	GRIK3 GLUR7	Homo sapiens (human)	10	0
Q15637	Splicing factor 1	SF1 ZFM1 ZNF162	Homo sapiens (human)	10	2
Q04206	Transcription factor p65	RELA NFKB3	Homo sapiens (human)	10	2
Q9UJA9	Ectonucleotide pyrophosphatase/phosphodiesterase family member 5	ENPP5	Homo sapiens (human)	10	8
P05186	Alkaline phosphatase, tissue-nonspecific isozyme	ALPL	Homo sapiens (human)	10	38	ARC syndrome Ehlers-Danlos syndrome Laron syndrome Loeffler syndrome Werner syndrome achondroplasia acoustic neuroma adult hypophosphatasia allergic asthma anemia angiomatous meningioma ankylosing spondylitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthrogryposis, renal dysfunction, and cholestasis 1 arthropathy asthma atherosclerosis autosomal recessive osteopetrosis 7 benign meningioma bone disease bone osteosarcoma breast cancer breast carcinoma calcinosis calcium metabolism disease campomelic dysplasia cancer cartilage disease cerebral convexity meningioma childhood hypophosphatasia chondrocalcinosis clear cell meningioma colitis connective tissue disease coronary artery disease craniosynostosis dental caries dentin caries depressive disorder diabetes mellitus dysthymic disorder embryoma embryonal carcinoma enophthalmos eosinophilic pneumonia epilepsy fibrous meningioma focal epilepsy gastroenteritis generalized anxiety disorder glomerulonephritis hereditary elliptocytosis hypercalcemia hyperostosis hyperphosphatemic familial tumoral calcinosis hypophosphatasia ileitis ileocolitis infantile hypophosphatasia inherited metabolic disorder intraorbital meningioma intraventricular meningioma intrinsic asthma keratosis follicularis kidney disease macrocytic anemia major depressive disorder melancholic depression meningioma meningothelial meningioma microcystic meningioma mongolian spot mucopolysaccharidosis IV multiple epiphyseal dysplasia musculoskeletal system disease nephritis nephrocalcinosis nephrolithiasis nephrosis neurotic disorder nutmeg liver obesity obsolete exophthalmos obsolete melancholia olfactory groove meningioma orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteomalacia osteopetrosis osteoporosis osteosarcoma osteosclerosis parasagittal meningioma partial motor epilepsy phobic disorder phosphorus metabolism disease pituitary adenoma polyhydramnios progeria prostate cancer prostate carcinoma psammomatous meningioma pseudoxanthoma elasticum pulmonary eosinophilia pyoureter rickets schizophrenia 10 schizophrenia secondary hyperparathyroidism secretory meningioma spinal meningioma transitional meningioma type 2 diabetes mellitus uric acid nephrolithiasis visual epilepsy
O60704	Protein-tyrosine sulfotransferase 2	TPST2	Homo sapiens (human)	10	3
P21583	Kit ligand	KITLG MGF SCF	Homo sapiens (human)	10	3
Q8WUT4	Leucine-rich repeat neuronal protein 4	LRRN4 C20orf75	Homo sapiens (human)	10	6
Q9NS62	Thrombospondin type-1 domain-containing protein 1	THSD1 TMTSP	Homo sapiens (human)	10	2
Q8TCU5	Glutamate receptor ionotropic, NMDA 3A	GRIN3A KIAA1973	Homo sapiens (human)	10	1
Q9UFP1	Golgi-associated kinase 1A	GASK1A C3orf41 FAM198A	Homo sapiens (human)	10	3
Q5ZPR3	CD276 antigen	CD276 B7H3	Homo sapiens (human)	10	78

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