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 **17326 - 17350** 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
Q8WUT4	Leucine-rich repeat neuronal protein 4	LRRN4 C20orf75	Homo sapiens (human)	10	6
Q14264	Endogenous retrovirus group 3 member 1 Env polyprotein	ERV3-1 ERV3	Homo sapiens (human)	9	6
P17858	ATP-dependent 6-phosphofructokinase, liver type	PFKL	Homo sapiens (human)	3	6	Down syndrome Lafora disease Unverricht-Lundborg syndrome arteriosclerotic cardiovascular disease atherosclerosis bipolar disorder coronary artery disease cystinuria dentatorubral-pallidoluysian atrophy early myoclonic encephalopathy galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma liver cancer mood disorder obsolete major affective disorder 1 obsolete major affective disorder 2 progressive myoclonus epilepsy 1A progressive myoclonus epilepsy tetralogy of Fallot ventricular septal defect
Q5VU97	VWFA and cache domain-containing protein 1	CACHD1 KIAA1573 VWCD1	Homo sapiens (human)	5	6
O76061	Stanniocalcin-2	STC2	Homo sapiens (human)	8	6
Q14697	Neutral alpha-glucosidase AB	GANAB G2AN KIAA0088	Homo sapiens (human)	3	6	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic liver disease
Q9P2J2	Protein turtle homolog A	IGSF9 IGSF9A KIAA1355 NRT1	Homo sapiens (human)	5	6
P36268	Inactive glutathione hydrolase 2	GGT2P GGT2	Homo sapiens (human)	7	6
Q9H1E5	Thioredoxin-related transmembrane protein 4	TMX4 KIAA1162 TXNDC13	Homo sapiens (human)	2	6
A2VDJ0	Transmembrane protein 131-like	TMEM131L KIAA0922	Homo sapiens (human)	13	6
O14638	Ectonucleotide pyrophosphatase/phosphodiesterase family member 3	ENPP3 PDNP3	Homo sapiens (human)	13	6	acute myeloid leukemia adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma allergic rhinitis benign mastocytoma bile duct adenocarcinoma bile duct cancer bile duct carcinoma cancer carcinoma cholangiocarcinoma choriocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer embryoma endometriosis of ovary endometriosis of uterus endometriosis extracutaneous mastocytoma hepatocellular carcinoma idiopathic scoliosis large intestine cancer liver cancer mast cell neoplasm mast-cell leukemia mastocytosis papillary renal cell carcinoma placenta cancer renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma urticaria pigmentosa vasomotor rhinitis wheat allergy
P13727	Bone marrow proteoglycan	PRG2 MBP	Homo sapiens (human)	7	6	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 Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 Pick's disease Reye syndrome allergic asthma asthma 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 breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration cholera colorectal cancer colorectal carcinoma congenital muscular dystrophy dermatophytosis dilated cardiomyopathy 1A dilated cardiomyopathy distal myopathy embryoma endometrial cancer endometrial carcinoma eosinophilic esophagitis facioscapulohumeral muscular dystrophy fungal infectious disease intrinsic asthma large intestine cancer limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma muscular dystrophy myelofibrosis myofibrillar myopathy 1 myofibrillar myopathy 3 nodular prostate 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 prostatic adenoma rippling muscle disease 2 uterine corpus cancer
P05783	Keratin, type I cytoskeletal 18	KRT18 CYK18	Homo sapiens (human)	20	6
P22079	Lactoperoxidase	LPO SAPX	Homo sapiens (human)	4	6
Q03167	Transforming growth factor beta receptor type 3	TGFBR3	Homo sapiens (human)	9	6
P18850	Cyclic AMP-dependent transcription factor ATF-6 alpha	ATF6	Homo sapiens (human)	9	6
Q9H4D0	Calsyntenin-2	CLSTN2 CS2	Homo sapiens (human)	6	6
P45877	Peptidyl-prolyl cis-trans isomerase C	PPIC CYPC	Homo sapiens (human)	1	6
Q68BL7	Olfactomedin-like protein 2A	OLFML2A	Homo sapiens (human)	2	6
Q2WGJ9	Fer-1-like protein 6	FER1L6 C8orfK23	Homo sapiens (human)	3	6
Q13002	Glutamate receptor ionotropic, kainate 2	GRIK2 GLUR6	Homo sapiens (human)	9	6
Q86YD3	Transmembrane protein 25	TMEM25	Homo sapiens (human)	8	6
Q9GZR5	Very long chain fatty acid elongase 4	ELOVL4	Homo sapiens (human)	2	6	Kuhnt-Junius degeneration Leber congenital amaurosis Sjogren-Larsson syndrome Stargardt disease achromatopsia acquired color blindness acquired hyperkeratosis acute myocardial infarction age related macular degeneration alternating hemiplegia of childhood angioedema anhidrosis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis blindness blue color blindness cancer cardiac arrest central nervous system disease cerebellar ataxia cerebellar disease color blindness cone-rod dystrophy 2 cone-rod dystrophy 7 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis dissociated nystagmus dry eye syndrome epilepsy erythrokeratodermia variabilis et progressiva 1 erythrokeratodermia variabilis eye disease fundus albipunctatus glycogen storage disease II granuloma annulare hepatocellular carcinoma hypertropia hypohidrosis ichthyosis inguinal hernia keratosis follicularis liver cancer locked-in syndrome macular degeneration mechanical strabismus mongolian spot myocardial infarction nervous system disease neurodegenerative disease night blindness obsolete congenital ichthyosiform erythroderma ophthalmoplegia pathologic nystagmus pseudoxanthoma elasticum quadriplegia red color blindness red-green color blindness retinitis pigmentosa 25 retinitis pigmentosa 30 retinitis pigmentosa silent myocardial infarction skin disease spinocerebellar ataxia type 34 spontaneous ocular nystagmus strabismus thrombocytopenia type 2 diabetes mellitus urticaria visual epilepsy xerophthalmia
O14524	Nuclear envelope integral membrane protein 1	NEMP1 KIAA0286 TMEM194 TMEM194A	Homo sapiens (human)	2	6
P40197	Platelet glycoprotein V	GP5	Homo sapiens (human)	8	6

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