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 **1626 - 1650** 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
O70354	Carbonic anhydrase-related protein 11	Ca11 Car11 Carp2	Mus musculus (house mouse)	3	7
Q9BX67	Junctional adhesion molecule C	JAM3	Homo sapiens (human)	2	7
P04035	3-hydroxy-3-methylglutaryl-coenzyme A reductase	HMGCR	Homo sapiens (human)	5	7
Q9ULC0	Endomucin	EMCN EMCN2 MUC14	Homo sapiens (human)	17	7
Q8IWT6	Volume-regulated anion channel subunit LRRC8A	LRRC8A KIAA1437 LRRC8 SWELL1	Homo sapiens (human)	3	7
Q8K209	Adhesion G-protein coupled receptor G1	Adgrg1 Cyt28 Gpr56	Mus musculus (house mouse)	7	7
Q3UY51	Leucine-rich repeat-containing protein 55	Lrrc55 Gm351	Mus musculus (house mouse)	3	7
P70211	Netrin receptor DCC	Dcc	Mus musculus (house mouse)	8	7
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
P08697	Alpha-2-antiplasmin	SERPINF2 AAP PLI	Homo sapiens (human)	8	7
Q5JS37	NHL repeat-containing protein 3	NHLRC3	Homo sapiens (human)	5	7
A0A2R8VHF1	RIKEN cDNA D430041D05 gene	D430041D05Rik	Mus musculus (house mouse)	6	7
Q3TVI8	Pre-B-cell leukemia transcription factor-interacting protein 1	Pbxip1 Hpip	Mus musculus (house mouse)	2	7
P24592	Insulin-like growth factor-binding protein 6	IGFBP6 IBP6	Homo sapiens (human)	16	7
Q6AYA5	Transmembrane protein 106B	Tmem106b	Rattus norvegicus (Norway rat)	5	7
Q15149	Plectin	PLEC PLEC1	Homo sapiens (human)	11	7
P02649	Apolipoprotein E	APOE	Homo sapiens (human)	11	7
P21802	Fibroblast growth factor receptor 2	FGFR2 BEK KGFR KSAM	Homo sapiens (human)	10	7
Q14114	Low-density lipoprotein receptor-related protein 8	LRP8 APOER2	Homo sapiens (human)	14	7
Q8R4G0	Netrin-G1	Ntng1 Kiaa0976 Lmnt1	Mus musculus (house mouse)	6	7
O60279	Sushi domain-containing protein 5	SUSD5 KIAA0527	Homo sapiens (human)	17	7
Q4ZIN3	Membralin	TMEM259 C19orf6	Homo sapiens (human)	1	7
Q8K2I4	Beta-mannosidase	Manba Bmn	Mus musculus (house mouse)	10	7
Q96FM1	Post-GPI attachment to proteins factor 3	PGAP3 CAB2 PERLD1	Homo sapiens (human)	1	7	Cogan syndrome Crohn's colitis Crohn's disease Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma bipolar disorder blepharospasm breast cancer breast carcinoma bruxism capillary disease congenital diaphragmatic hernia congenital disorder of glycosylation craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated cleft palate learning disability lingual-facial-buccal dyskinesia monocular esotropia movement disease oligohydramnios scoliosis situs inversus stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis ulcerative colitis visual epilepsy
Q86UU0	B-cell CLL/lymphoma 9-like protein	BCL9L DLNB11	Homo sapiens (human)	12	7

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