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 **107251 - 107275** 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
Q9ER88	Small ribosomal subunit protein mS29	Dap3 Mrps29	Mus musculus (house mouse)	0	1
P53611	Geranylgeranyl transferase type-2 subunit beta	RABGGTB GGTB	Homo sapiens (human)	0	1
Q5T442	Gap junction gamma-2 protein	GJC2 GJA12	Homo sapiens (human)	1	1
Q86VR7	V-set and immunoglobulin domain-containing protein 10-like	VSIG10L	Homo sapiens (human)	10	1
Q61656	Probable ATP-dependent RNA helicase DDX5	Ddx5 Tnz2	Mus musculus (house mouse)	2	1
P25648	Mediator of RNA polymerase II transcription subunit 12	SRB8 GIG1 MED12 NUT6 SSN5	Saccharomyces cerevisiae S288C	2	1
Q16891	MICOS complex subunit MIC60	IMMT HMP MIC60 MINOS2	Homo sapiens (human)	0	1
A0A0B4J1E2	SNW domain-containing protein 1	Snw1	Mus musculus (house mouse)	0	1
Q8JZS0	Protein lin-7 homolog A	Lin7a Mals1 Veli1	Mus musculus (house mouse)	3	1
Q9Z2C8	Y-box-binding protein 2	Ybx2 Msy2	Mus musculus (house mouse)	0	1
Q9NVK5	FGFR1 oncogene partner 2	FGFR1OP2	Homo sapiens (human)	0	1
A0A2I3BRL8	Predicted gene 7324	Gm7324	Mus musculus (house mouse)	0	1
Q5VZM2	Ras-related GTP-binding protein B	RRAGB	Homo sapiens (human)	1	1
O60927	E3 ubiquitin-protein ligase PPP1R11	PPP1R11 HCGV TCTE5	Homo sapiens (human)	2	1
O08528	Hexokinase-2	Hk2	Mus musculus (house mouse)	0	1
Q9CPN9	Protease, serine 3B	Prss3b 2210010C04Rik trypsinogen	Mus musculus (house mouse)	0	1
F4JDC2	YTH domain-containing family protein	ECT2	Arabidopsis thaliana (thale cress)	0	1
Q9ES74	Serine/threonine-protein kinase Nek7	Nek7	Mus musculus (house mouse)	0	1
Q8N335	Glycerol-3-phosphate dehydrogenase 1-like protein	GPD1L KIAA0089	Homo sapiens (human)	0	1	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation congestive heart failure coronary artery disease head and neck squamous cell carcinoma nutmeg liver osteoarthritis sick sinus syndrome steatotic liver disease sudden infant death syndrome
P30085	UMP-CMP kinase	CMPK1 CMK CMPK UCK UMK UMPK	Homo sapiens (human)	4	1
Q14207	Protein NPAT	NPAT CAND3 E14	Homo sapiens (human)	4	1
P43897	Elongation factor Ts, mitochondrial	TSFM	Homo sapiens (human)	0	1
Q9BZE4	GTP-binding protein 4	GTPBP4 CRFG NOG1	Homo sapiens (human)	1	1
Q15054	DNA polymerase delta subunit 3	POLD3 KIAA0039	Homo sapiens (human)	3	1
Q01968	Inositol polyphosphate 5-phosphatase OCRL	OCRL OCRL1	Homo sapiens (human)	1	1	Bartter disease Conn's syndrome Dent disease Ehlers-Danlos syndrome Fanconi anemia Fanconi syndrome Laron syndrome Waterhouse-Friderichsen syndrome achondroplasia amblyopia anemia angular cheilitis anxiety disorder arthritis arthropathy attention deficit hyperactivity disorder autistic disorder autoimmune hemolytic anemia azoospermia blindness buphthalmos calcinosis calcium metabolism disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cheilitis chromosome 17p13.1 deletion syndrome chronic kidney disease chronic ulcer of skin congenital nystagmus cryptorchidism cystinosis dental caries dental enamel hypoplasia dentin caries depressive disorder diabetes insipidus dissociated nystagmus dysthymic disorder epilepsy esophagitis fetal erythroblastosis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma gingivitis glaucoma glioblastoma glomerulonephritis high grade glioma hydrocephalus hydrophthalmos hypercalcemia hyperparathyroidism hypertropia hypokalemia hypophosphatemia inguinal hernia intellectual disability isolated elevated serum creatine phosphokinase levels kidney failure learning disability lip disease lissencephaly listeriosis macrocytic anemia major depressive disorder mechanical strabismus melancholic depression microphthalmia neonatal anemia nephritis nephrocalcinosis nephrolithiasis neurohypophyseal diabetes insipidus neurotic disorder obsolete constipation obsolete melancholia oculocerebrorenal syndrome omphalocele ophthalmoplegia osteitis fibrosa osteoarthritis osteogenesis imperfecta osteomalacia otitis media pathologic nystagmus peptic esophagitis periodontitis phosphorus metabolism disease primary hyperaldosteronism proteinuria recurrent corneal erosion renal tubular acidosis rickets scoliosis skin benign neoplasm skin cancer spondyloepimetaphyseal dysplasia, Sponastrime type spontaneous ocular nystagmus stereotypic movement disorder strabismic amblyopia strabismus subcortical band heterotopia thrombocytopenia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue umbilical hernia uremia uric acid nephrolithiasis visual epilepsy

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