GlyCosmos Portal

Displaying entries **13126 - 13150** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q13303	Voltage-gated potassium channel subunit beta-2	KCNAB2 KCNA2B KCNK2	2	1
P21817	Ryanodine receptor 1	RYR1 RYDR	2	2
Q9H2D6	TRIO and F-actin-binding protein	TRIOBP KIAA1662 TARA	2	1
O95977	Sphingosine 1-phosphate receptor 4	S1PR4 EDG6	2	0
Q9NRE1	Matrix metalloproteinase-26	MMP26	2	0
Q969H0	F-box/WD repeat-containing protein 7	FBXW7 FBW7 FBX30 SEL10	2	1
H0YFM8	Adhesion G protein-coupled receptor G6 (Fragment)	ADGRG6	2	0
Q9UKZ9	Procollagen C-endopeptidase enhancer 2	PCOLCE2 PCPE2	2	2
Q7Z3T9	Neuropilin	DKFZp686J1169	2	0
Q8N2K0	Lysophosphatidylserine lipase ABHD12	ABHD12 C20orf22	2	5
Q8NHE4	V-type proton ATPase subunit e 2	ATP6V0E2 ATP6V0E2L C7orf32	2	3
Q496F6	CMRF35-like molecule 2	CD300E CD300LE CLM2 CMRF35A5 IREM2	2	2
Q86WJ1	Chromodomain-helicase-DNA-binding protein 1-like	CHD1L ALC1	2	2
A0A7I2V2T9	Laminin subunit beta 1	LAMB1	2	0
Q7Z406	Myosin-14	MYH14 KIAA2034	2	2
Q96QF7	Germ cell nuclear acidic protein	GCNA ACRC	2	1
A0A3B3ISD7	Complement C4B (Chido blood group) (Fragment)	C4B	2	0
P24723	Protein kinase C eta type	PRKCH PKCL PRKCL	2	4
P08237	ATP-dependent 6-phosphofructokinase, muscle type	PFKM PFKX	2	1	D-bifunctional protein deficiency adenocarcinoma adenoma anemia breast cancer breast carcinoma cancer carcinoma carnitine palmitoyltransferase I deficiency cholecystolithiasis choledocholithiasis cholelithiasis coronary artery disease cribriform carcinoma cystinuria diabetes mellitus embryoma galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease gout granular cell carcinoma hemolytic anemia hepatocellular carcinoma high grade glioma hyperglycemia hyperuricemia liver cancer liver carcinoma macrocytic anemia pancreatic cancer pancreatic carcinoma pseudosarcomatous fibromatosis renal tubular acidosis sarcomatoid carcinoma schizophrenia tuberculosis tubular adenocarcinoma type 2 diabetes mellitus
Q9P109	Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4	GCNT4	2	0
Q9Y2H0	Disks large-associated protein 4	DLGAP4 DAP4 KIAA0964 SAPAP4	2	2
Q8NGE7	Olfactory receptor 9K2	OR9K2	2	0
Q9UKI8	Serine/threonine-protein kinase tousled-like 1	TLK1 KIAA0137	2	2
Q96L58	Beta-1,3-galactosyltransferase 6	B3GALT6	2	7	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease Hirschsprung's disease Laron syndrome Rothmund-Thomson syndrome achondroplasia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease bone disease cartilage disease cherubism chondrodysplasia punctata chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate clubfoot collagen disease collecting duct carcinoma connective tissue disease cutis laxa enophthalmos exostosis heart septal defect hepatocellular carcinoma intellectual disability isolated cleft palate isolated ectopia lentis learning disability liver cancer mal de Meleda mitral valve insufficiency mitral valve prolapse myopia nonpapillary renal cell carcinoma obsolete exophthalmos orbital disease osteogenesis imperfecta osteoporosis papillary renal cell carcinoma paraplegia patent foramen ovale periarthritis renal carcinoma renal cell carcinoma restrictive dermopathy sarcomatoid renal cell carcinoma scoliosis spinal cord disease tendinitis ventricular septal defect
Q17RA0	Interleukin 6 signal transducer (Gp130, oncostatin M receptor)	IL6ST	2	0

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