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 **125201 - 125225** 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
Q7TQA1	Immunoglobulin superfamily member 1	Igsf1 Kiaa0364	Mus musculus (house mouse)	12	9
P08F94	Fibrocystin	PKHD1 FCYT TIGM1	Homo sapiens (human)	66	9
Q04721	Neurogenic locus notch homolog protein 2	NOTCH2	Homo sapiens (human)	17	9
O95450	A disintegrin and metalloproteinase with thrombospondin motifs 2	ADAMTS2 PCINP PCPNI	Homo sapiens (human)	11	9
Q0VBD0	Integrin beta-8	Itgb8	Mus musculus (house mouse)	6	9
P26012	Integrin beta-8	ITGB8	Homo sapiens (human)	7	9
P22304	Iduronate 2-sulfatase	IDS SIDS	Homo sapiens (human)	9	9	Balo concentric sclerosis Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome Fabry disease Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Griscelli syndrome Laron syndrome Marfan syndrome Sveinsson chorioretinal atrophy Waardenburg syndrome type 3 X-linked ichthyosis achondroplasia adrenoleukodystrophy agammaglobulinemia allergic asthma alternating hemiplegia of childhood amnestic disorder antiphospholipid syndrome asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer brain disease breast cancer breast carcinoma cancer central nervous system disease centronuclear myopathy X-linked centronuclear myopathy cerebral infarction cerebrovascular disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital adrenal hyperplasia congenital central hypoventilation syndrome congenital ptosis congenital structural myopathy congestive heart failure craniosynostosis cystinuria depressive disorder diarrhea dysthymic disorder embryoma epilepsy fragile X syndrome galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease glycoproteinosis heart valve disease hydrocephalus hypercalcemia hypertrichosis hypoglycemia inguinal hernia intellectual disability intrinsic asthma learning disability lipid storage disease lung benign neoplasm lung carcinoma lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis myeloproliferative neoplasm myocarditis myotonic disease myotonic dystrophy type 2 narcolepsy nephrocalcinosis nervous system disease neurotic disorder obsolete intestinal pseudo-obstruction obsolete melancholia obstructive hydrocephalus obstructive sleep apnea ocular albinism with sensorineural deafness oculocutaneous albinism omphalocele optic papillitis osteochondrodysplasia ovarian cancer ovarian carcinoma pancytopenia papilledema paralytic ileus phosphorus metabolism disease post-traumatic stress disorder ptosis retinal edema retrograde amnesia rumination disorder senile degeneration of brain sensorineural hearing loss sick sinus syndrome situs inversus sleep apnea sudden infant death syndrome trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis umbilical hernia visual epilepsy
F1MAN8	Laminin subunit alpha 5	Lama5	Rattus norvegicus (Norway rat)	9	9
Q9R013	Cathepsin F	Ctsf	Mus musculus (house mouse)	6	9
Q61625	Glutamate receptor ionotropic, delta-2	Grid2	Mus musculus (house mouse)	6	9
P15509	Granulocyte-macrophage colony-stimulating factor receptor subunit alpha	CSF2RA CSF2R CSF2RY	Homo sapiens (human)	11	9
P06797	Procathepsin L	Ctsl Ctsl1	Mus musculus (house mouse)	3	9
Q9Z2G6	Protein sel-1 homolog 1	Sel1l Sel1h	Mus musculus (house mouse)	8	9
Q3V346	Low density lipoprotein receptor-related protein 2	Lrp2	Mus musculus (house mouse)	4	9
Q13508	Ecto-ADP-ribosyltransferase 3	ART3 TMART	Homo sapiens (human)	2	9	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
Q64449	C-type mannose receptor 2	Mrc2 Kiaa0709	Mus musculus (house mouse)	14	9
Q80TR1	Adhesion G protein-coupled receptor L1	Adgrl1 Kiaa0821 Lec2 Lphn1	Mus musculus (house mouse)	8	9
Q9NXH8	Torsin-4A	TOR4A C9orf167	Homo sapiens (human)	1	9
Q8VBZ3	Putative lipid scramblase CLPTM1	Clptm1 N14	Mus musculus (house mouse)	6	9
Q69ZQ1	Myogenesis-regulating glycosidase	Myorg Kiaa1161 Net37	Mus musculus (house mouse)	8	9
P70275	Semaphorin-3E	Sema3e Semah Semh	Mus musculus (house mouse)	5	9
P28351	Alpha-galactosidase A	aglA	Aspergillus niger	7	9
Q8BXA5	Lipid scramblase CLPTM1L	Clptm1l	Mus musculus (house mouse)	3	9
Q9NTN9	Semaphorin-4G	SEMA4G KIAA1619	Homo sapiens (human)	6	9
Q53F39	Metallophosphoesterase 1	MPPE1 PGAP5	Homo sapiens (human)	1	9	bipolar disorder borderline personality disorder cancer cerebral malaria chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis B hepatitis influenza intermittent explosive disorder malaria melanoma papillary renal cell carcinoma pneumonia renal cell carcinoma sarcomatoid renal cell carcinoma skin melanoma

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