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 **17626 - 17650** 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
Q99250	Sodium channel protein type 2 subunit alpha	SCN2A HBA NAC2 SCN2A1 SCN2A2	Homo sapiens (human)	10	1
U3KPZ7	RNA-binding protein 27	LOC127814297	Homo sapiens (human)	10	1
Q6P179	Endoplasmic reticulum aminopeptidase 2	ERAP2 LRAP	Homo sapiens (human)	10	43
P30530	Tyrosine-protein kinase receptor UFO	AXL UFO	Homo sapiens (human)	10	17
P21802	Fibroblast growth factor receptor 2	FGFR2 BEK KGFR KSAM	Homo sapiens (human)	10	7
O60500	Nephrin	NPHS1 NPHN	Homo sapiens (human)	10	0
P55268	Laminin subunit beta-2	LAMB2 LAMS	Homo sapiens (human)	10	62
Q9BZV3	Interphotoreceptor matrix proteoglycan 2	IMPG2 IPM200	Homo sapiens (human)	10	0
Q13740	CD166 antigen	ALCAM MEMD	Homo sapiens (human)	10	162
P17813	Endoglin	ENG END	Homo sapiens (human)	10	5
Q96JH7	Deubiquitinating protein VCPIP1	VCPIP1 KIAA1850 VCIP135	Homo sapiens (human)	10	3
P78324	Tyrosine-protein phosphatase non-receptor type substrate 1	SIRPA BIT MFR MYD1 PTPNS1 SHPS1 SIRP	Homo sapiens (human)	10	50
P24928	DNA-directed RNA polymerase II subunit RPB1	POLR2A POLR2	Homo sapiens (human)	10	2
Q7Z442	Polycystin-1-like protein 2	PKD1L2 KIAA1879 PC1L2	Homo sapiens (human)	10	1	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease
Q6AI39	BRD4-interacting chromatin-remodeling complex-associated protein-like	BICRAL GLTSCR1L KIAA0240	Homo sapiens (human)	10	3
Q5XPI4	E3 ubiquitin-protein ligase RNF123	RNF123 KPC1	Homo sapiens (human)	10	2
Q10471	Polypeptide N-acetylgalactosaminyltransferase 2	GALNT2	Homo sapiens (human)	10	3	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 achondroplasia acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease diabetes mellitus embryoma essential hypertension familial hyperlipidemia gastric adenocarcinoma gliosarcoma hepatocellular carcinoma high grade glioma hyperalphalipoproteinemia 1 hyperglycemia hypertension hypochondroplasia inflammatory bowel disease 1 inflammatory bowel disease liver cancer mixed glioma nutmeg liver obesity papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma type 2 diabetes mellitus ulcerative colitis
Q96NR3	Patched domain-containing protein 1	PTCHD1	Homo sapiens (human)	10	0
Q86V15	Zinc finger protein castor homolog 1	CASZ1 CST SRG ZNF693	Homo sapiens (human)	10	1
Q5T0B9	Zinc finger protein 362	ZNF362	Homo sapiens (human)	10	1
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
P0DPD8	EEF1AKMT4-ECE2 readthrough transcript protein	EEF1AKMT4-ECE2	Homo sapiens (human)	10	1
Q9Y6L7	Tolloid-like protein 2	TLL2 KIAA0932	Homo sapiens (human)	10	5
P54578	Ubiquitin carboxyl-terminal hydrolase 14	USP14 TGT	Homo sapiens (human)	10	1
Q9H756	Leucine-rich repeat-containing protein 19	LRRC19	Homo sapiens (human)	10	0

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