GlyCosmos Portal

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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 **118701 - 118725** 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
Q642U8	Pre-glycoprotein polyprotein GP complex	GPC	Mammarenavirus juninense	7	0
P43096	Secreted aspartic protease 7	SAP7	Candida albicans	7	0
B4QMF4	Protein cueball	cue	Drosophila simulans	7	0
A2AI20	Glutamate receptor	Grin1	Mus musculus (house mouse)	7	0
P40002	Transcriptional regulator MIT1	MIT1	Saccharomyces cerevisiae S288C	7	1
Q9WTQ2	Podocalyxin	Podxl Pclp1	Rattus norvegicus (Norway rat)	7	0
Q03600	Integrin alpha ina-1	ina-1	Caenorhabditis elegans	7	0
P16546	Spectrin alpha chain, non-erythrocytic 1	Sptan1 Spna2 Spta2	Mus musculus (house mouse)	7	7
O14514	Adhesion G protein-coupled receptor B1	ADGRB1 BAI1	Homo sapiens (human)	7	3
O54826	Protein AF-10	Mllt10 Af10	Mus musculus (house mouse)	7	1
Q16656	Nuclear respiratory factor 1	NRF1	Homo sapiens (human)	7	2
P24807	Signal transducer CD24	Cd24 Cd24a Ly-52	Mus musculus (house mouse)	7	0
Q3UR55	Sodium/potassium-transporting ATPase subunit beta	Atp1b2	Mus musculus (house mouse)	7	0
Q9M3D8	L-type lectin-domain containing receptor kinase I.3	LECRK13 AtLecRK2 SR1	Arabidopsis thaliana (thale cress)	7	0
O43426	Synaptojanin-1	SYNJ1 KIAA0910	Homo sapiens (human)	7	1	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 Creutzfeldt-Jakob disease Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 1 Parkinson's disease 20 Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia amnestic disorder amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autistic disorder 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 bipolar disorder blepharospasm blindness borderline personality disorder brain disease cerebral degeneration cone-rod dystrophy congenital muscular dystrophy congenital nystagmus congenital ptosis dementia developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 53 dissociated nystagmus distal myopathy dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset Parkinson's disease epilepsy esophagitis facioscapulohumeral muscular dystrophy focal hand dystonia fundus albipunctatus gastroesophageal reflux disease giant cell glioblastoma glioblastoma high grade glioma intellectual disability intermittent explosive disorder isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia locked-in syndrome microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma neurodegenerative disease 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 infantile epileptic encephalopathy oculopharyngeal muscular dystrophy optic atrophy pathologic nystagmus peptic esophagitis progressive muscular atrophy ptosis quadriplegia retinal degeneration retinitis pigmentosa retrograde amnesia rhabdomyosarcoma rippling muscle disease 2 scoliosis secondary Parkinson disease spontaneous ocular nystagmus status epilepticus tauopathy tooth agenesis visual epilepsy
Q9C8E7	Glutamate receptor 3.3	GLR3.3	Arabidopsis thaliana (thale cress)	7	0
Q9P0X4	Voltage-dependent T-type calcium channel subunit alpha-1I	CACNA1I KIAA1120	Homo sapiens (human)	7	1
P0C959	Dipeptidyl-peptidase 5	AFUA_2G09030	Aspergillus fumigatus Af293	7	0
Q22398	Zinc metalloproteinase nas-22	nas-22	Caenorhabditis elegans	7	0
E6XTV3	Hemagglutinin	HA	Influenza A virus (A/Netherlands/002P1/1951(H1N1))	7	0
P26572	Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	MGAT1 GGNT1 GLCT1 GLYT1 MGAT	Homo sapiens (human)	7	2	Balo concentric sclerosis adrenoleukodystrophy breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease central nervous system cancer central nervous system disease complex partial epilepsy congestive heart failure cystinuria diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health disease of metabolism embryoma endomyocardial fibrosis epilepsy galactokinase deficiency galactosemia gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycine encephalopathy glycogen storage disease Ia glycogen storage disease heart disease hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease liver cancer mixed glioma multiple sclerosis narcolepsy nervous system disease obesity obsolete type 1 diabetes mellitus 9 prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder temporal lobe epilepsy type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus visual epilepsy
D2CFR5	Pre-glycoprotein polyprotein GP complex	GPC	Mammarenavirus juninense	7	0
Q8R332	Nucleoporin p58/p45	Nup58 Nupl1	Mus musculus (house mouse)	7	1
P16067	Atrial natriuretic peptide receptor 2	Npr2	Rattus norvegicus (Norway rat)	7	0
B1XLD2	beta-N-acetylhexosaminidase	SYNPCC7002_A0075	Picosynechococcus sp. PCC 7002	7	0

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