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 **15051 - 15075** 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
Q96FF9	Sororin	CDCA5	Homo sapiens (human)	0	1
Q96GX1	Tectonic-2	TCTN2 C12orf38 TECT2	Homo sapiens (human)	4	0
P35232	Prohibitin 1	PHB1 PHB	Homo sapiens (human)	5	3
P48551	Interferon alpha/beta receptor 2	IFNAR2 IFNABR IFNARB	Homo sapiens (human)	6	9
O75157	TSC22 domain family protein 2	TSC22D2 KIAA0669 TILZ4	Homo sapiens (human)	9	2
P22413	Ectonucleotide pyrophosphatase/phosphodiesterase family member 1	ENPP1 M6S1 NPPS PC1 PDNP1	Homo sapiens (human)	10	45	Ehlers-Danlos syndrome HCL-V Laron syndrome McCune Albright syndrome X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne acquired hyperkeratosis acute myocardial infarction adult astrocytic tumor allergic asthma amelogenesis imperfecta anaplastic astrocytoma anemia angioid streaks ankylosing spondylitis ankylosis aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arterial calcification of infancy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autosomal dominant hypophosphatemic rickets autosomal recessive hypophosphatemic rickets autosomal recessive osteopetrosis 7 bicuspid aortic valve disease bile duct adenocarcinoma bile duct cancer bile duct carcinoma bile duct disease blindness bone disease brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cardiovascular system disease carotid artery disease cartilage disease cerebral infarction cerebrovascular disease childhood astrocytic tumor childhood cerebral astrocytoma cholangiocarcinoma chondrocalcinosis chronic kidney disease colorectal cancer colorectal carcinoma congenital hypothyroidism congenital toxoplasmosis congestive heart failure connective tissue disease coronary artery disease coronary thrombosis craniosynostosis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis endometriosis of ovary endometriosis of uterus endometriosis enthesopathy essential hypertension exanthem fibrillary astrocytoma gemistocytic astrocytoma gestational diabetes giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance hairy cell leukemia heart disease hepatitis C hepatocellular carcinoma hereditary elliptocytosis herpes simplex high grade glioma hypercalcemia hypercementosis hyperglycemia hyperinsulinism hyperphosphatemic familial tumoral calcinosis hypertension hypophosphatemia hypothyroidism insulinoma intermittent claudication intrinsic asthma juvenile pilocytic astrocytoma keratosis follicularis kidney disease kidney failure large intestine cancer linear nevus sebaceous syndrome liver cancer lung benign neoplasm lung cancer lung carcinoma macrocytic anemia malignant astrocytoma melanoma mitral valve insufficiency mitral valve prolapse mongolian spot monoclonal gammopathy of uncertain significance morbid obesity mucopolysaccharidosis IV multiple epiphyseal dysplasia multiple myeloma musculoskeletal system disease myelitis myocardial infarction myopia myxedema nephritis nephrocalcinosis nephrosis neurogenic arthropathy nodular prostate nonepidermolytic palmoplantar keratoderma nutmeg liver obesity obsolete type 1 diabetes mellitus 9 ossification of the posterior longitudinal ligament of spine osteoarthritis osteochondrodysplasia osteogenesis imperfecta osteomalacia osteopetrosis osteoporosis osteosclerosis otitis media palmoplantar keratosis pancreatic cancer pancreatic carcinoma periarthritis perinatal intestinal perforation peripheral artery disease peripheral vascular disease phosphorus metabolism disease pilocytic astrocytoma plasmacytoma pneumocystosis polycystic ovary syndrome polycythemia vera polycythemia postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma pseudoxanthoma elasticum pulmonary valve stenosis pyoureter restrictive cardiomyopathy retinal disease retinitis rheumatoid arthritis rickets sarcomatoid carcinoma scoliosis sensorineural hearing loss silent myocardial infarction skin melanoma spondyloarthropathy spondylosis steatotic liver disease subependymal giant cell astrocytoma suppurative periapical periodontitis tendinitis tropical sprue tympanosclerosis 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 viral infectious disease
E9PMI5	Serpin family H member 1 (Fragment)	SERPINH1	Homo sapiens (human)	2	0
Q0PQ42	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
Q15762	CD226 antigen	CD226 DNAM1	Homo sapiens (human)	8	1
P62750	Large ribosomal subunit protein uL23	RPL23A	Homo sapiens (human)	2	2
Q9BXW7	Haloacid dehalogenase-like hydrolase domain-containing 5	HDHD5 CECR5	Homo sapiens (human)	1	1
O43448	Voltage-gated potassium channel subunit beta-3	KCNAB3 KCNA3B	Homo sapiens (human)	0	1
P43694	Transcription factor GATA-4	GATA4	Homo sapiens (human)	2	1
V9HW77	Creatine kinase B-type	HEL-211	Homo sapiens (human)	0	1
P0DPD8	EEF1AKMT4-ECE2 readthrough transcript protein	EEF1AKMT4-ECE2	Homo sapiens (human)	10	1
Q9NRG4	N-lysine methyltransferase SMYD2	SMYD2 KMT3C	Homo sapiens (human)	0	1
A0A2U7N3G4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8NGL2	Olfactory receptor 5L1	OR5L1	Homo sapiens (human)	2	0
Q9Y6L7	Tolloid-like protein 2	TLL2 KIAA0932	Homo sapiens (human)	10	5
A6NCI4	von Willebrand factor A domain-containing protein 3A	VWA3A	Homo sapiens (human)	1	0
P35408	Prostaglandin E2 receptor EP4 subtype	PTGER4 PTGER2	Homo sapiens (human)	1	0
Q9Y399	Small ribosomal subunit protein uS2m	MRPS2	Homo sapiens (human)	0	1
P30260	Cell division cycle protein 27 homolog	CDC27 ANAPC3 D0S1430E D17S978E	Homo sapiens (human)	4	3
Q8SP64	MHC class I (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q16515	Acid-sensing ion channel 2	ASIC2 ACCN ACCN1 BNAC1 MDEG	Homo sapiens (human)	6	0

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