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 **12676 - 12700** of **126547** in total

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UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96LR9	Apolipoprotein L domain-containing protein 1	APOLD1 VERGE	Homo sapiens (human)	3	1
Q96LR5	Ubiquitin-conjugating enzyme E2 E2	UBE2E2 UBCH8	Homo sapiens (human)	0	1
Q96LQ0	Protein phosphatase 1 regulatory subunit 36	PPP1R36 C14orf50	Homo sapiens (human)	0	1
Q96LM1	Putative uncharacterized protein encoded by LINC00615	LINC00615 C12orf37	Homo sapiens (human)	0	1
Q96LL4	Uncharacterized protein C8orf48	C8orf48	Homo sapiens (human)	3	1
Q96LK0	Centrosomal protein of 19 kDa	CEP19 C3orf34	Homo sapiens (human)	0	1
Q96LI9	Uncharacterized protein CXorf58	CXorf58	Homo sapiens (human)	2	1
Q96LI5	CCR4-NOT transcription complex subunit 6-like	CNOT6L CCR4B	Homo sapiens (human)	1	2
Q96LD1	Zeta-sarcoglycan	SGCZ	Homo sapiens (human)	2	1
Q96LC7	Sialic acid-binding Ig-like lectin 10	SIGLEC10 SLG2	Homo sapiens (human)	6	4	B-cell lymphoma cancer childhood leukemia leukemia obsolete ymphosarcoma
Q96LB9	Peptidoglycan recognition protein 3	PGLYRP3 PGRPIA	Homo sapiens (human)	1	0
Q96LB8	Peptidoglycan recognition protein 4	PGLYRP4 PGRPIB	Homo sapiens (human)	5	0
Q96LB3	Intraflagellar transport protein 74 homolog	IFT74 CCDC2 CMG1	Homo sapiens (human)	2	2
Q96LB2	Mas-related G-protein coupled receptor member X1	MRGPRX1 MRGX1 SNSR3 SNSR4	Homo sapiens (human)	1	0
Q96LA9	Mas-related G-protein coupled receptor member X4	MRGPRX4 MRGX4 SNSR5 SNSR6	Homo sapiens (human)	2	0
Q96LA6	Fc receptor-like protein 1	FCRL1 FCRH1 IFGP1 IRTA5	Homo sapiens (human)	1	0
Q96LA5	Fc receptor-like protein 2	FCRL2 FCRH2 IFGP4 IRTA4 SPAP1	Homo sapiens (human)	5	0
Q96L96	Alpha-protein kinase 3	ALPK3 KIAA1330 MAK	Homo sapiens (human)	2	1
Q96L92	Sorting nexin-27	SNX27 KIAA0488	Homo sapiens (human)	0	1
Q96L91	E1A-binding protein p400	EP400 CAGH32 KIAA1498 KIAA1818 TNRC12	Homo sapiens (human)	57	4
Q96L73	Histone-lysine N-methyltransferase, H3 lysine-36 specific	NSD1 ARA267 KMT3B	Homo sapiens (human)	2	1
Q96L58	Beta-1,3-galactosyltransferase 6	B3GALT6	Homo sapiens (human)	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	Homo sapiens (human)	2	0
Q96L35	receptor protein-tyrosine kinase	EPHB4	Homo sapiens (human)	1	0
Q96L34	MAP/microtubule affinity-regulating kinase 4	MARK4 KIAA1860 MARKL1	Homo sapiens (human)	0	1

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