GlyCosmos Portal

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96LI9	Uncharacterized protein CXorf58	CXorf58	2	1
Q96LI5	CCR4-NOT transcription complex subunit 6-like	CNOT6L CCR4B	1	2
Q96LD1	Zeta-sarcoglycan	SGCZ	2	1
Q96LC7	Sialic acid-binding Ig-like lectin 10	SIGLEC10 SLG2	6	4	B-cell lymphoma cancer childhood leukemia leukemia obsolete ymphosarcoma
Q96LB9	Peptidoglycan recognition protein 3	PGLYRP3 PGRPIA	1	0
Q96LB8	Peptidoglycan recognition protein 4	PGLYRP4 PGRPIB	5	0
Q96LB3	Intraflagellar transport protein 74 homolog	IFT74 CCDC2 CMG1	2	2
Q96LB2	Mas-related G-protein coupled receptor member X1	MRGPRX1 MRGX1 SNSR3 SNSR4	1	0
Q96LA9	Mas-related G-protein coupled receptor member X4	MRGPRX4 MRGX4 SNSR5 SNSR6	2	0
Q96LA6	Fc receptor-like protein 1	FCRL1 FCRH1 IFGP1 IRTA5	1	0
Q96LA5	Fc receptor-like protein 2	FCRL2 FCRH2 IFGP4 IRTA4 SPAP1	5	0
Q96L96	Alpha-protein kinase 3	ALPK3 KIAA1330 MAK	2	1
Q96L92	Sorting nexin-27	SNX27 KIAA0488	0	1
Q96L91	E1A-binding protein p400	EP400 CAGH32 KIAA1498 KIAA1818 TNRC12	57	4
Q96L73	Histone-lysine N-methyltransferase, H3 lysine-36 specific	NSD1 ARA267 KMT3B	2	1
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
Q96L42	Potassium voltage-gated channel subfamily H member 8	KCNH8	2	0
Q96L35	receptor protein-tyrosine kinase	EPHB4	1	0
Q96L34	MAP/microtubule affinity-regulating kinase 4	MARK4 KIAA1860 MARKL1	0	1
Q96L15	Ecto-ADP-ribosyltransferase 5	ART5	3	1	cholera
Q96L12	Calreticulin-3	CALR3 CRT2	2	0	cardiomyopathy cataract endomyocardial fibrosis familial hypertrophic cardiomyopathy hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy vitiligo
Q96L08	Sushi domain-containing protein 3	SUSD3	1	0
Q96KX2	F-actin-capping protein subunit alpha-3	CAPZA3 CAPAA3 GSG3	1	1
Q96KX1	Uncharacterized protein C4orf36	C4orf36	0	1
Q96KW9	Sperm acrosome-associated protein 7	SPACA7 C13orf28	2	0

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