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 **14951 - 14975** 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
Q8N7K0	Zinc finger protein 433	ZNF433	Homo sapiens (human)	0	1
Q86T90	Protein hinderin	KIAA1328	Homo sapiens (human)	0	1
Q5SRE5	Nucleoporin NUP188	NUP188 KIAA0169	Homo sapiens (human)	1	1
Q4V339	Zinc-regulated GTPase metalloprotein activator 1F	ZNG1F CBWD6 CBWD7	Homo sapiens (human)	0	1
B6KP76	Mitochondrial carrier domain-containing protein	BN1205_039580	Toxoplasma gondii VEG	0	1
B9PXE4	40S ribosomal protein S4	BN1205_040740	Toxoplasma gondii VEG	0	1
A0JNY3	Gephyrin	Gphn	Mus musculus (house mouse)	0	1
Q4DHG7	MIF4G domain-containing protein	Tc00.1047053506445.20	Trypanosoma cruzi strain CL Brener	0	1
Q9P055	JNK1/MAPK8-associated membrane protein	JKAMP C14orf100 JAMP	Homo sapiens (human)	2	1
Q3U276	Succinate dehydrogenase assembly factor 1, mitochondrial	Sdhaf1 Lyrm8	Mus musculus (house mouse)	0	1
O88600	Heat shock 70 kDa protein 4	Hspa4 Hsph2 Irp94	Rattus norvegicus (Norway rat)	0	1
P32900	Protein SKG6	SKG6	Saccharomyces cerevisiae S288C	5	1
Q9Y4X5	E3 ubiquitin-protein ligase ARIH1	ARIH1 ARI MOP6 UBCH7BP	Homo sapiens (human)	0	1
Q9Y259	Choline/ethanolamine kinase	CHKB CHETK CHKL	Homo sapiens (human)	1	1	Balo concentric sclerosis Bell's palsy Duchenne muscular dystrophy X-linked dilated cardiomyopathy adrenoleukodystrophy agnosia 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 bronchus cancer bronchus carcinoma campomelic dysplasia central nervous system disease centronuclear myopathy 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 muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy craniometaphyseal dysplasia cytochrome-c oxidase deficiency disease developmental coordination disorder 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 facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy inherited metabolic disorder isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy microcephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcolepsy 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 oculopharyngeal muscular dystrophy recurrent hypersomnia restless legs syndrome rigid spine muscular dystrophy 1 rippling muscle disease 2
Q9R1X4	Protein timeless homolog	Timeless Tim1 Timeless1	Mus musculus (house mouse)	1	1
Q6ZSJ8	Uncharacterized protein C1orf122	C1orf122	Homo sapiens (human)	0	1
Q86U86	Protein polybromo-1	PBRM1 BAF180 PB1	Homo sapiens (human)	3	1
Q8NEJ9	Neuroguidin	NGDN C14orf120	Homo sapiens (human)	0	1
Q4D0E4	Uncharacterized protein	Tc00.1047053510031.30	Trypanosoma cruzi strain CL Brener	0	1
A2AGK3	Butyrobetaine (gamma), 2-oxoglutarate dioxygenase 1 (gamma-butyrobetaine hydroxylase) (Fragment)	Bbox1	Mus musculus (house mouse)	0	1
P30613	Pyruvate kinase PKLR	PKLR PK1 PKL	Homo sapiens (human)	0	1	Gaucher's disease acquired polycythemia anemia breast cancer breast carcinoma cancer cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis colorectal cancer colorectal carcinoma congenital hemolytic anemia congenital nonspherocytic hemolytic anemia depressive disorder diabetes mellitus diabetic ketoacidosis episodic kinesigenic dyskinesia 1 erythropoietin polycythemia familial erythrocytosis 1 familial erythrocytosis 2 favism gallbladder cancer gallbladder carcinoma hematopoietic system disease hemoglobinopathy hemolytic anemia hepatocellular carcinoma hereditary elliptocytosis hereditary sensory neuropathy type 4 hereditary sensory neuropathy hyperglycemia large intestine cancer liver cancer lung benign neoplasm macrocytic anemia major depressive disorder malaria melancholic depression obsolete melancholia optic atrophy 1 optic atrophy pancreatic cancer pancreatic carcinoma polycythemia vera polycythemia primary polycythemia prostate cancer prostate carcinoma pyruvate kinase deficiency of red cells sensory peripheral neuropathy stress polycythemia thalassemia type 2 diabetes mellitus
Q7TSH3	Zinc finger protein 516	Znf516 Kiaa0222 Zfp516	Mus musculus (house mouse)	0	1
V5BRQ8	Alcohol dehydrogenase	TCDM_02375	Trypanosoma cruzi Dm28c	0	1
Q4D1I7	Uncharacterized protein	Tc00.1047053509721.10	Trypanosoma cruzi strain CL Brener	0	1
Q9Z2I0	Mitochondrial proton/calcium exchanger protein	Letm1	Mus musculus (house mouse)	0	1

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