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 **5726 - 5750** 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
Q9UPZ3	BLOC-2 complex member HPS5	HPS5 AIBP63 KIAA1017	Homo sapiens (human)	0	1
A0A0U1RQT3	Heparan sulfate proteoglycan 2 (Fragment)	HSPG2	Homo sapiens (human)	2	0
A0A493QP75	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q14520	Hyaluronan-binding protein 2	HABP2 HGFAL PHBP	Homo sapiens (human)	8	3
Q8N7Z5	Ankyrin repeat domain-containing protein 31	ANKRD31	Homo sapiens (human)	0	1
Q86TZ1	Tetratricopeptide repeat protein 6	TTC6 C14orf25 NCRNA00291	Homo sapiens (human)	1	1
Q5PT55	Sodium/bile acid cotransporter 5	SLC10A5	Homo sapiens (human)	3	0
O94953	Lysine-specific demethylase 4B	KDM4B JHDM3B JMJD2B KIAA0876	Homo sapiens (human)	0	1
P54803	Galactocerebrosidase	GALC	Homo sapiens (human)	6	5	Evans' syndrome Fabry disease Farber lipogranulomatosis Gaucher's disease Krabbe disease Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wolman disease amblyopia autoimmune thrombocytopenic purpura bipolar disorder blindness bronchus cancer bronchus carcinoma cancer cerebellar ataxia cerebellar disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital nystagmus demyelinating disease depressive disorder disease of metabolism dissociated nystagmus dysthymic disorder embryoma epilepsy glycogen storage disease II head and neck cancer head and neck squamous cell carcinoma hydrocephalus hypertropia inflammatory bowel disease laryngeal disease late onset Parkinson's disease leukodystrophy lipid storage disease low tension glaucoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease major depressive disorder mechanical strabismus melancholic depression metachromatic leukodystrophy multiple sclerosis nasopharynx carcinoma neurodegenerative disease neurotic disorder obsolete melancholia obstructive hydrocephalus ophthalmoplegia optic atrophy osteomalacia paraplegia pathologic nystagmus placental insufficiency primary open angle glaucoma relapsing fever rickets schizophrenia senile degeneration of brain sensorineural hearing loss sphingolipidosis spontaneous ocular nystagmus squamous cell carcinoma status epilepticus strabismic amblyopia strabismus systemic lupus erythematosus tongue squamous cell carcinoma tracheal disease visual epilepsy
A0A0E3DCU9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
S5DHQ4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9H444	Charged multivesicular body protein 4b	CHMP4B C20orf178 SHAX1	Homo sapiens (human)	0	1
P47890	Olfactory receptor 1G1	OR1G1 OR1G2	Homo sapiens (human)	1	0
Q6ZTR5	Cilia- and flagella-associated protein 47	CFAP47 CHDC2 CXorf22 CXorf30 CXorf59	Homo sapiens (human)	3	1
Q9BXP2	Solute carrier family 12 member 9	SLC12A9 CCC6 CIP1	Homo sapiens (human)	2	3
P62745	Rho-related GTP-binding protein RhoB	RHOB ARH6 ARHB	Homo sapiens (human)	2	0
Q63ZY3	KN motif and ankyrin repeat domain-containing protein 2	KANK2 ANKRD25 KIAA1518 MXRA3 SIP	Homo sapiens (human)	2	1
X5D7A8	Cell adhesion molecule 1 isoform A (Fragment)	CADM1	Homo sapiens (human)	3	0
Q5TH69	Brefeldin A-inhibited guanine nucleotide-exchange protein 3	ARFGEF3 BIG3 C6orf92 KIAA1244	Homo sapiens (human)	1	1
P0C6S8	Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3	LINGO3 LERN2 LRRN6B	Homo sapiens (human)	9	4
P37837	Transaldolase	TALDO1 TAL TALDO TALDOR	Homo sapiens (human)	0	1	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease T-cell acute lymphoblastic leukemia acatalasia allergic asthma anemia asthma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer capillary disease childhood T-cell acute lymphoblastic leukemia childhood leukemia chronic kidney disease diabetes mellitus diabetic ketoacidosis disease of metabolism gallbladder disease head and neck squamous cell carcinoma hemangioma of liver hepatocellular carcinoma hereditary hemorrhagic telangiectasia immune system disease intrinsic asthma leukemia liver cancer liver cirrhosis liver disease macrocytic anemia multiple sclerosis obsolete T-cell lymphoblastic leukemia/lymphoma oligohydramnios osteomalacia pancytopenia patent ductus arteriosus patent foramen ovale placental insufficiency rickets sensorineural hearing loss sickle cell anemia skin benign neoplasm skin cancer squamous cell carcinoma telangiectasis thrombocytopenia tongue squamous cell carcinoma type 2 diabetes mellitus ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
P61165	Transmembrane protein 258	TMEM258 C11orf10	Homo sapiens (human)	0	1
Q9BWU0	Kanadaptin	SLC4A1AP	Homo sapiens (human)	1	1
Q9Y5S9	RNA-binding protein 8A	RBM8A RBM8	Homo sapiens (human)	0	1
A0A1W1B5J9	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0

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