GlyCosmos Portal

GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen, GlyConnect, GlycoProtDB and The O-GlcNAc Database. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

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 **16251 - 16275** 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
Q9HAN9	Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1	NMNAT1 NMNAT	Homo sapiens (human)	0	1
Q86XT4	E3 ubiquitin-protein ligase TRIM50	TRIM50 TRIM50A	Homo sapiens (human)	0	1
P40926	Malate dehydrogenase, mitochondrial	MDH2	Homo sapiens (human)	2	2	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome acute myocardial infarction adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma agnosia aniridia brain ischemia bronchiolo-alveolar adenocarcinoma brucellosis cancer carcinoma cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma cocaine dependence collecting duct carcinoma congenital adrenal hyperplasia congestive heart failure coronary thrombosis depressive disorder developmental and epileptic encephalopathy 51 diabetes mellitus diabetic ketoacidosis duodenum cancer dysthymic disorder dystonia embryoma endometrial cancer endometrial carcinoma epilepsy gastritis glomerulonephritis heart cancer heroin dependence hypercalcemia hypertensive retinopathy hypertropia kidney disease lung cancer lung non-small cell carcinoma major depressive disorder mechanical strabismus melancholic depression melanoma morphine dependence myocardial infarction nephritis nephrocalcinosis nephrosis neurotic disorder obsolete constipation obsolete melancholia ophthalmoplegia opiate dependence ovarian carcinoma panic disorder papillary renal cell carcinoma paraganglioma pheochromocytoma phosphorus metabolism disease prostate cancer prostate carcinoma proteinuria pyoureter renal carcinoma renal cell carcinoma renal osteodystrophy sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma small intestine cancer strabismus substance abuse substance-related disorder uterine cancer uterine corpus cancer visual epilepsy
W6S1K2	MHC class I polypeptide-related sequence A (Fragment)	MICA	Homo sapiens (human)	3	0
Q9UM22	Mammalian ependymin-related protein 1	EPDR1 MERP1 UCC1	Homo sapiens (human)	4	2
Q96M89	Coiled-coil domain-containing protein 138	CCDC138	Homo sapiens (human)	2	4
O00571	ATP-dependent RNA helicase DDX3X	DDX3X DBX DDX3	Homo sapiens (human)	8	2
O94892	Zinc finger protein 432	ZNF432 KIAA0798	Homo sapiens (human)	1	2
P49767	Vascular endothelial growth factor C	VEGFC	Homo sapiens (human)	4	3
P31943	Heterogeneous nuclear ribonucleoprotein H	HNRNPH1 HNRPH HNRPH1	Homo sapiens (human)	7	6
Q8NBL1	Protein O-glucosyltransferase 1	POGLUT1 C3orf9 CLP46 KTELC1 MDSRP	Homo sapiens (human)	5	23	Dowling-Degos disease Duchenne muscular dystrophy T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia acute myeloid leukemia 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 childhood T-cell acute lymphoblastic leukemia childhood leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital muscular dystrophy distal myopathy embryoma essential thrombocythemia facioscapulohumeral muscular dystrophy hematopoietic system disease isolated elevated serum creatine phosphokinase levels keratosis follicularis large intestine cancer leukemia limb-girdle muscular dystrophy lung cancer lung non-small cell carcinoma mongolian spot muscular dystrophy myelodysplastic syndrome 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 primary biliary cholangitis pseudoxanthoma elasticum reticulate acropigmentation of Kitamura rippling muscle disease 2
Q9NWR8	Calcium uniporter regulatory subunit MCUb, mitochondrial	MCUB CCDC109B	Homo sapiens (human)	0	1
Q5H943	Kita-kyushu lung cancer antigen 1	CT83 CXorf61 KKLC1	Homo sapiens (human)	1	0
Q9ULU8	Calcium-dependent secretion activator 1	CADPS CAPS CAPS1 KIAA1121	Homo sapiens (human)	1	1
O75445	Usherin	USH2A	Homo sapiens (human)	67	2
P62851	Small ribosomal subunit protein eS25	RPS25	Homo sapiens (human)	0	1
Q6P7N7	Transmembrane protein 81	TMEM81	Homo sapiens (human)	2	1
Q9NQW7	Xaa-Pro aminopeptidase 1	XPNPEP1 XPNPEPL XPNPEPL1	Homo sapiens (human)	1	1
Q8NGC8	Olfactory receptor 11H7	OR11H7 OR11H7P	Homo sapiens (human)	1	0
Q13510	Acid ceramidase	ASAH1 ASAH	Homo sapiens (human)	8	123	Albright's hereditary osteodystrophy Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Beckwith-Wiedemann syndrome Bell's palsy CLOVES syndrome Erdheim-Chester disease Ewing sarcoma Fabry disease Farber lipogranulomatosis IGSF1 deficiency syndrome Krabbe disease Laron syndrome Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Perlman syndrome Pick's disease Reye syndrome Sotos syndrome Turner syndrome Unverricht-Lundborg syndrome Usher syndrome type 2 Usher syndrome type 3 Usher syndrome Wolman disease achondroplasia acute monocytic leukemia acute myeloid leukemia adult medulloblastoma agnosia amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease arthritis arthropathy atrial fibrillation autosomal recessive distal hereditary motor neuronopathy 1 benign ependymoma benign epilepsy with centrotemporal spikes blepharospasm brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cellular ependymoma cerebral degeneration childhood ependymoma childhood medulloblastoma chylomicron retention disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined saposin deficiency congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus cystic fibrosis dementia dentatorubral-pallidoluysian atrophy developmental coordination disorder dissociated nystagmus early myoclonic encephalopathy embryoma epilepsy facial nerve disease facial paralysis focal hand dystonia gastroenteritis gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gonadal dysgenesis head and neck cancer head and neck squamous cell carcinoma herpes simplex high grade glioma hyperglycemia hypoparathyroidism hypothyroidism idiopathic generalized epilepsy idiopathic interstitial pneumonia ileitis ileocolitis intellectual disability invasive ductal carcinoma large intestine cancer lateral sclerosis learning disability lipid storage disease lung benign neoplasm lung cancer lung carcinoma lysosomal storage disease measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma motor neuron disease myxedema myxopapillary ependymoma neonatal diabetes neurodegenerative disease neuroectodermal tumor obesity ocular melanoma osteoporosis pancreatic cancer pancreatic carcinoma papillary carcinoma papillary ependymoma pathologic nystagmus pneumonia postinflammatory pulmonary fibrosis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma pseudohypoparathyroidism type IB pseudohypoparathyroidism pseudopseudohypoparathyroidism pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent corneal erosion retinitis pigmentosa-deafness syndrome retinoblastoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis sensorineural hearing loss skin melanoma speech disorder spinal muscular atrophy with progressive myoclonic epilepsy spinal muscular atrophy spontaneous ocular nystagmus tanycytic ependymoma thyroid adenoma thyroid cancer thyroid gland carcinoma transient neonatal diabetes mellitus viral infectious disease
P46779	Large ribosomal subunit protein eL28	RPL28	Homo sapiens (human)	1	2
P30711	Glutathione S-transferase theta-1	GSTT1	Homo sapiens (human)	0	1
Q9UNW1	Multiple inositol polyphosphate phosphatase 1	MINPP1 MIPP	Homo sapiens (human)	7	15	actinic keratosis cancer carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer head and neck cancer large intestine cancer multiple myeloma nodular goiter papillary adenocarcinoma papillary renal cell carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis skin disease spinal cord disease thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma
W0NW49	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
A0A1C4HDW6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0

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