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 **115801 - 115825** 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
P12555	Hemagglutinin-neuraminidase	HN	Newcastle disease virus strain D26/76	6	0
Q4WUK7	Lytic polysaccharide monooxygenase-like protein X325	X325	Aspergillus fumigatus Af293	6	0
A9JR10	Pre-glycoprotein polyprotein GP complex	GPC	Mammarenavirus machupoense	6	0
P06870	Kallikrein-1	KLK1	Homo sapiens (human)	6	28
Q9FWX7	ABC transporter B family member 11	ABCB11 MDR8 PGP11	Arabidopsis thaliana (thale cress)	6	0
C4QZV7	Pheromone-processing carboxypeptidase KEX1	KEX1	Komagataella phaffii GS115	6	0
Q63028	Alpha-adducin	Add1	Rattus norvegicus (Norway rat)	6	1
A0A0G2JL69	Complement C2	C2	Homo sapiens (human)	6	0
P04663	Hemagglutinin (Fragment)	HA	Influenza A virus (A/Queensland/7/70(H3N2))	6	0
Q4V3B3	Beta-glucosidase 28	BGLU28	Arabidopsis thaliana (thale cress)	6	0
E9ESM3	Pheromone-processing carboxypeptidase KEX1	KEX1	Metarhizium robertsii ARSEF 23	6	0
A2A863	Integrin beta-4	Itgb4	Mus musculus (house mouse)	6	2
Q07977	Alpha-2,8-sialyltransferase 8B	St8sia2 Siat8b Stx	Rattus norvegicus (Norway rat)	6	0
P29341	Polyadenylate-binding protein 1	Pabpc1 Pabp1	Mus musculus (house mouse)	6	1
Q92186	Alpha-2,8-sialyltransferase 8B	ST8SIA2 SIAT8B STX	Homo sapiens (human)	6	0	adenocarcinoma adenoma allergic rhinitis anaplastic astrocytoma autism spectrum disorder autistic disorder bipolar disorder breast cancer breast carcinoma cancer childhood cerebral astrocytoma colitis cribriform carcinoma diarrhea disease of mental health embryoma epilepsy fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma granular cell carcinoma hemolytic-uremic syndrome high grade glioma ileitis ileocolitis intestinal infectious disease juvenile pilocytic astrocytoma lung cancer lung non-small cell carcinoma malignant astrocytoma mood disorder neuroblastoma pilocytic astrocytoma protoplasmic astrocytoma psychotic disorder rhabdomyosarcoma schizophrenia shigellosis subependymal giant cell astrocytoma tubular adenocarcinoma vasomotor rhinitis
Q9XSY9	Osteopontin	SPP1 OPN	Ovis aries (sheep)	6	0
Q8K021	Secretory carrier-associated membrane protein 1	Scamp1	Mus musculus (house mouse)	6	3
P68756	Hemagglutinin (Fragment)	HA	Influenza B virus (strain B/finland/146/90)	6	0
Q84NC9	Tricyclene synthase 1e20, chloroplastic	1e20	Antirrhinum majus (snapdragon)	6	0
P0DN87	Choriogonadotropin subunit beta 7	CGB7	Homo sapiens (human)	6	0
O00451	GDNF family receptor alpha-2	GFRA2 GDNFRB RETL2 TRNR2	Homo sapiens (human)	6	6	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease adenocarcinoma adenoma bipolar disorder cancer colorectal cancer colorectal carcinoma follicular adenoma frontotemporal dementia hepatocellular carcinoma large intestine cancer lingual-facial-buccal dyskinesia liver cancer microcystic adenoma neuroblastoma neuropathy pancreatic cancer pancreatic carcinoma papillary adenoma peripheral nervous system disease polyneuropathy preretinal fibrosis schizophrenia secondary Parkinson disease
Q9H6E4	Coiled-coil domain-containing protein 134	CCDC134	Homo sapiens (human)	6	2
A0A0F7IQ06	Alpha v integrin	Itgav	Mus musculus (house mouse)	6	0
Q07837	Amino acid transporter heavy chain SLC3A1	SLC3A1 NBAT	Homo sapiens (human)	6	37	IgA glomerulonephritis Marfan syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction 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 bulimia nervosa calcinosis calcium metabolism disease cancer chronic kidney disease colon carcinoma colorectal cancer congenital myasthenic syndrome 22 congenital ptosis coronary thrombosis cystinuria diabetes mellitus diabetic ketoacidosis distal myopathy epilepsy essential hypertension facioscapulohumeral muscular dystrophy galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease high grade glioma hypercalcemia hypertension hypoglycemia hypogonadism hypotonia-cystinuria syndrome interstitial nephritis kidney failure lactic acidosis limb-girdle muscular dystrophy muscular dystrophy myocardial infarction nephrocalcinosis nephrolithiasis nephrosclerosis 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 panic disorder phosphorus metabolism disease primary pulmonary hypertension prostate cancer prostate carcinoma ptosis pyelitis pyelonephritis renal hypertension renal infectious disease silent myocardial infarction situs inversus synovial sarcoma tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis urinary tract obstruction vesicoureteral reflux visual epilepsy
Q9NIV1	Eukaryotic translation initiation factor 2-alpha kinase	PEK EIF2AK3	Drosophila melanogaster (fruit fly)	6	0

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