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 **3576 - 3600** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
Q96QL5	PSG4 protein	PSG4	Homo sapiens (human)	3	0
P18031	Tyrosine-protein phosphatase non-receptor type 1	PTPN1 PTP1B	Homo sapiens (human)	3	1
Q9UHI7	Solute carrier family 23 member 1	SLC23A1 SVCT1 YSPL3	Homo sapiens (human)	3	0
Q9Y6M0	Testisin	PRSS21 ESP1 TEST1	Homo sapiens (human)	3	4	Behcet's disease Down syndrome acquired immunodeficiency syndrome alcohol dependence alcohol use disorder atrial fibrillation cancer cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood germ cell cancer diabetes mellitus diabetic ketoacidosis disorder of sexual development embryonal cancer germ cell and embryonal cancer germ cell cancer germinoma hepatitis B hermaphroditism human immunodeficiency virus infectious disease monoclonal gammopathy of uncertain significance monoclonal paraproteinemia ovarian cancer ovarian carcinoma plasma cell neoplasm pseudohermaphroditism type 2 diabetes mellitus
Q13304	Uracil nucleotide/cysteinyl leukotriene receptor	GPR17	Homo sapiens (human)	3	0
Q9BXR3	Endogenous retrovirus group K member 6 Pol protein	ERVK-6 ERVK6	Homo sapiens (human)	3	0
C9JH43	Neuronal cell adhesion molecule (Fragment)	NRCAM	Homo sapiens (human)	3	0
Q9BZE9	Tether containing UBX domain for GLUT4	ASPSCR1 ASPL RCC17 TUG UBXD9 UBXN9	Homo sapiens (human)	3	1
Q3YBR2	Transforming growth factor beta regulator 1	TBRG1 NIAM	Homo sapiens (human)	3	1
Q8TCW9	Prokineticin receptor 1	PROKR1 GPR73 PKR1	Homo sapiens (human)	3	0
C1KBH7	Fibroblast growth factor receptor 1 isoform 3	FGFR1	Homo sapiens (human)	3	0
Q5NDL2	EGF domain-specific O-linked N-acetylglucosamine transferase	EOGT AER61 C3orf64 EOGT1	Homo sapiens (human)	3	7	Adams-Oliver syndrome Clouston syndrome alopecia arteriovenous malformation autosomal recessive polycystic kidney disease cataract clubfoot communicating hydrocephalus epilepsy hydrocephalus hypertropia intellectual disability learning disability leukopenia mechanical strabismus microphthalmia obstructive hydrocephalus ophthalmoplegia periventricular leukomalacia polycystic kidney disease 4 portal hypertension primary pulmonary hypertension senile degeneration of brain strabismus tetralogy of Fallot thrombocytopenia visual epilepsy
Q13087	Protein disulfide-isomerase A2	PDIA2 PDIP	Homo sapiens (human)	3	8
Q9BQ87	F-box-like/WD repeat-containing protein TBL1Y	TBL1Y TBL1	Homo sapiens (human)	3	1
Q8N3Y3	Xylosyl- and glucuronyltransferase LARGE2	LARGE2 GYLTL1B	Homo sapiens (human)	3	5	Duchenne muscular dystrophy acute myocardial infarction autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cancer congenital muscular dystrophy coronary thrombosis distal myopathy embryoma facioscapulohumeral muscular dystrophy limb-girdle muscular dystrophy muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy prostate cancer prostate carcinoma rippling muscle disease 2 silent myocardial infarction transitional cell carcinoma
P80723	Brain acid soluble protein 1	BASP1 NAP22	Homo sapiens (human)	3	1
P28288	ATP-binding cassette sub-family D member 3	ABCD3 PMP70 PXMP1	Homo sapiens (human)	3	1
Q86VY4	Testis-specific Y-encoded-like protein 5	TSPYL5 KIAA1750	Homo sapiens (human)	3	1
Q9UNQ2	Probable dimethyladenosine transferase	DIMT1 DIMT1L	Homo sapiens (human)	3	1
Q96EB1	Elongator complex protein 4	ELP4 C11orf19 PAXNEB	Homo sapiens (human)	3	2
Q8N370	Large neutral amino acids transporter small subunit 4	SLC43A2 LAT4	Homo sapiens (human)	3	1
P53621	Coatomer subunit alpha	COPA	Homo sapiens (human)	3	5
Q8IUC8	Polypeptide N-acetylgalactosaminyltransferase 13	GALNT13 KIAA1918	Homo sapiens (human)	3	2	cancer chronic obstructive pulmonary disease lung benign neoplasm lung carcinoma sickle cell anemia
Q99705	Melanin-concentrating hormone receptor 1	MCHR1 GPR24 SLC1	Homo sapiens (human)	3	0
P13224	Platelet glycoprotein Ib beta chain	GP1BB	Homo sapiens (human)	3	1

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