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 **15151 - 15175** 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
A0A2H4RN79	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q9P2X0	Dolichol-phosphate mannosyltransferase subunit 3	DPM3	Homo sapiens (human)	2	2	Duchenne muscular dystrophy 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 cardiomyopathy clubfoot congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy muscular dystrophy 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 rippling muscle disease 2
P54578	Ubiquitin carboxyl-terminal hydrolase 14	USP14 TGT	Homo sapiens (human)	10	1
B1AMP9	Sulfatase 2 (Fragment)	SULF2	Homo sapiens (human)	1	0
C0KJW4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q7Z410	Transmembrane protease serine 9	TMPRSS9	Homo sapiens (human)	4	0
Q92564	DCN1-like protein 4	DCUN1D4 KIAA0276	Homo sapiens (human)	1	2
P23246	Splicing factor, proline- and glutamine-rich	SFPQ PSF	Homo sapiens (human)	3	1
G0ZMJ9	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A0A7C4N8	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A5H2UFL9	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q9UEL6	Myelin protein zero like 1 (Fragment)	MPZL1	Homo sapiens (human)	1	0
Q8NA70	Protein FAM47B	FAM47B	Homo sapiens (human)	0	1
Q9H5K3	Protein O-mannose kinase	POMK SGK196	Homo sapiens (human)	5	9	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome 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 bilateral optic nerve hypoplasia blindness cardiomyopathy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly lung small cell carcinoma mechanical strabismus megalocornea microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopia 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly strabismus syndromic X-linked intellectual disability Najm type visual epilepsy
Q95IE1	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q13435	Splicing factor 3B subunit 2	SF3B2 SAP145	Homo sapiens (human)	0	1
P00338	L-lactate dehydrogenase A chain	LDHA	Homo sapiens (human)	3	7	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 B-cell lymphoma Ewing sarcoma Kawasaki disease Kennedy's disease Pick's disease Reye syndrome X-linked dilated cardiomyopathy acoustic neuroma acute myocardial infarction adenocarcinoma adenoma adult hepatocellular carcinoma adult medulloblastoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bile duct adenocarcinoma bile duct carcinoma bipolar disorder bladder carcinoma bone osteosarcoma borderline personality disorder brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cellular leiomyoma central nervous system cancer central nervous system lymphoma cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood hepatocellular carcinoma childhood leukemia childhood medulloblastoma childhood osteosarcoma cholangiocarcinoma chondrosarcoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma cutaneous Paget's disease cystinuria degenerative disc disease depressive disorder diabetes mellitus 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 arthrogryposis dysthymic disorder embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endomyocardial fibrosis esophagus squamous cell carcinoma essential thrombocythemia eye disease familial periodic paralysis familial retinoblastoma fibromyalgia galactosemia gallbladder cancer gallbladder carcinoma gastrointestinal stromal tumor gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma 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 goiter granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hyperglycemia hypertrophic cardiomyopathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis impetigo herpetiformis intellectual disability intermittent explosive disorder intrahepatic cholangiocarcinoma isolated elevated serum creatine phosphokinase levels kidney cancer kidney failure kwashiorkor large intestine cancer lateral meningocele syndrome learning disability leukemia liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lymphoma major depressive disorder marasmus medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningioma middle cerebral artery infarction mixed glioma mood disorder multiple myeloma multiple sclerosis myelitis myelofibrosis myocardial infarction myoglobinuria myopathy myositis nasopharynx carcinoma neuroblastoma neurotic disorder nodular prostate nonpapillary renal cell carcinoma nontoxic goiter nutrition disease obsolete melancholia obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma oxyphilic adenoma pancreatic cancer pancreatic carcinoma panic disorder papillary adenocarcinoma papillary renal cell carcinoma peptic ulcer disease pituitary adenoma pituitary cancer pituitary carcinoma postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma prostatic adenoma protein-energy malnutrition pseudosarcomatous fibromatosis pulmonary fibrosis renal carcinoma renal cell carcinoma renal oncocytoma retinoblastoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma trilateral retinoblastoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer uterine corpus sarcoma viral infectious disease
A0A2U3RU45	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
Q9NP73	UDP-N-acetylglucosamine transferase subunit ALG13	ALG13 CXorf45 GLT28D1	Homo sapiens (human)	0	1	Bell's palsy Meckel's diverticulum West syndrome agnosia attention deficit hyperactivity disorder autistic disorder blindness cerebral degeneration choreatic disease clubfoot congenital disorder of glycosylation type I congenital disorder of glycosylation congenital nystagmus craniosynostosis developmental and epileptic encephalopathy 36 dissociated nystagmus epilepsy facial nerve disease facial paralysis focal segmental glomerulosclerosis hypophosphatemia intellectual disability learning disability lung cancer lung non-small cell carcinoma microcephaly non-syndromic X-linked intellectual disability obesity obsolete infantile epileptic encephalopathy optic atrophy pathologic nystagmus placental insufficiency pyloric stenosis spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
G1ENH6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q14210	Lymphocyte antigen 6D	LY6D E48	Homo sapiens (human)	0	1
Q8N5J2	Ubiquitin carboxyl-terminal hydrolase MINDY-1	MINDY1 FAM63A KIAA1390	Homo sapiens (human)	0	1
A0A0K1NWU9	MHC class I polypeptide-related sequence A (Fragment)	MICA	Homo sapiens (human)	3	0
Q9Y450	HBS1-like protein	HBS1L HBS1 KIAA1038	Homo sapiens (human)	3	1
D5L9D8	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0

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