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 **14651 - 14675** 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
Q4DDN8	Vesicle-associated membrane protein, putative	Tc00.1047053507811.60	Trypanosoma cruzi strain CL Brener	0	1
K2NC20	Vesicle-associated membrane protein, putative	MOQ_009723	Trypanosoma cruzi marinkellei	0	1
Q8BH80	Vesicle-associated membrane protein, associated protein B and C	Vapb	Mus musculus (house mouse)	0	1
Q15836	Vesicle-associated membrane protein 3	VAMP3 SYB3	Homo sapiens (human)	0	1
P63044	Vesicle-associated membrane protein 2	Vamp2 Syb2	Mus musculus (house mouse)	2	2
O88384	Vesicle transport through interaction with t-SNAREs homolog 1B	Vti1b Vti1l1	Mus musculus (house mouse)	2	3
Q9UEU0	Vesicle transport through interaction with t-SNAREs homolog 1B	VTI1B VTI1 VTI1L VTI1L1 VTI2	Homo sapiens (human)	2	1
Q8WV19	Vesicle transport protein SFT2A	SFT2D1 C6orf83	Homo sapiens (human)	0	1
Q6QD59	Vesicle transport protein SEC20	Bnip1 Sec20 Sec20l	Mus musculus (house mouse)	1	2
Q12981	Vesicle transport protein SEC20	BNIP1 NIP1 SEC20L	Homo sapiens (human)	0	1
Q9NZ01	Very-long-chain enoyl-CoA reductase	TECR GPSN2 SC2	Homo sapiens (human)	2	1	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
Q9CY27	Very-long-chain enoyl-CoA reductase	Tecr Gpsn2	Mus musculus (house mouse)	2	1
Q3ZCD7	Very-long-chain enoyl-CoA reductase	TECR GPSN2	Bos taurus (cattle)	2	0
Q55C17	Very-long-chain enoyl-CoA reductase	gpsn2	Dictyostelium discoideum	2	0
Q64232	Very-long-chain enoyl-CoA reductase	Tecr Gpsn2	Rattus norvegicus (Norway rat)	2	0
Q53GQ0	Very-long-chain 3-oxoacyl-CoA reductase	HSD17B12 SDR12C1	Homo sapiens (human)	2	2	breast cancer breast carcinoma cancer carcinoma cardiovascular system disease diabetes mellitus disease of mental health embryoma head and neck squamous cell carcinoma heart disease idiopathic scoliosis intellectual disability invasive ductal carcinoma learning disability melanoma neuroblastoma ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma psychotic disorder sarcomatoid carcinoma schizophrenia skin melanoma type 2 diabetes mellitus
O70503	Very-long-chain 3-oxoacyl-CoA reductase	Hsd17b12 Kik1	Mus musculus (house mouse)	0	1
Q9P035	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 3	HACD3 BIND1 PTPLAD1	Homo sapiens (human)	1	2	depressive disorder dysthymic disorder major depressive disorder melancholic depression neurotic disorder obsolete melancholia
Q8K2C9	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 3	Hacd3 Ptplad1	Mus musculus (house mouse)	1	2
Q5RBK3	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2	HACD2 PTPLB	Pongo abelii (Sumatran orangutan)	1	0
Q2KIP8	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2	HACD2 PTPLB	Bos taurus (cattle)	1	0
Q6Y1H2	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2	HACD2 PTPLB	Homo sapiens (human)	1	1
Q9D3B1	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2	Hacd2 Ptplb	Mus musculus (house mouse)	1	1
Q4W1W1	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1	HACD1 PTPLA	Canis lupus familiaris (dog)	1	0
B0YJ81	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1	HACD1 PTPLA	Homo sapiens (human)	1	0	B-cell lymphoma Ehrlich tumor carcinoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Lyme disease Perry syndrome Streptococcus pneumonia T-cell acute lymphoblastic leukemia X-linked dilated cardiomyopathy achondroplasia acute biphenotypic leukemia acute leukemia agnosia allergic asthma allergic rhinitis androgen insensitivity syndrome anthrax disease aplastic anemia arrhythmogenic right ventricular cardiomyopathy asthma 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 beta thalassemia bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma cancer centronuclear myopathy cerebral infarction cerebrovascular disease cervix uteri carcinoma in situ childhood osteosarcoma clubfoot colitis common cold congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital myopathy 4A congenital ptosis congenital structural myopathy cryptococcosis cryptorchidism developmental coordination disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy embryoma epilepsy facioscapulohumeral muscular dystrophy gastroenteritis giant cell glioblastoma glioblastoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma ileitis ileocolitis influenza intellectual disability intrinsic asthma learning disability limb-girdle muscular dystrophy liver cancer liver cirrhosis mantle cell lymphoma megaconial type congenital muscular dystrophy multidrug-resistant tuberculosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy nemaline myopathy 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 obsolete ymphosarcoma oculopharyngeal muscular dystrophy ophthalmoplegia osteosarcoma ovarian cancer ovarian carcinoma paroxysmal nocturnal hemoglobinuria pleural empyema pneumonia polycystic ovary syndrome polyhydramnios premature menopause primary ovarian insufficiency prostate cancer prostate carcinoma ptosis recurrent hypersomnia rigid spine muscular dystrophy 1 scoliosis sick sinus syndrome steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder thalassemia thymic carcinoma thymoma tuberculosis type 2 diabetes mellitus type C thymoma vasomotor rhinitis viral infectious disease wheat allergy

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