GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **16651 - 16675** 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
Q9NPY3	Complement component C1q receptor	CD93 C1QR1 MXRA4	Homo sapiens (human)	5	2	Kuhnt-Junius degeneration acute leukemia acute myocardial infarction allergic asthma asthma cancer central nervous system cancer chronic fatigue syndrome coronary artery disease coronary thrombosis embryoma encephalitis encephalomyelitis giant cell glioblastoma glioblastoma gliosarcoma high grade glioma intrinsic asthma lung cancer lung non-small cell carcinoma mixed glioma myelitis myocardial infarction nasopharynx carcinoma parapsoriasis psoriasis pustulosis of palm and sole silent myocardial infarction vascular cancer
Q9NPZ5	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2	B3GAT2 GLCATS KIAA1963	Homo sapiens (human)	2	0	Barrett's esophagus schizophrenia thrombophilia
Q9NQ03	Transcriptional repressor scratch 2	SCRT2	Homo sapiens (human)	0	1
Q9NQ11	Polyamine-transporting ATPase 13A2	ATP13A2 PARK9	Homo sapiens (human)	2	1
Q9NQ25	SLAM family member 7	SLAMF7 CS1	Homo sapiens (human)	6	1
Q9NQ29	Putative RNA-binding protein Luc7-like 1	LUC7L LUC7L1	Homo sapiens (human)	0	1
Q9NQ30	Endothelial cell-specific molecule 1	ESM1	Homo sapiens (human)	1	0
Q9NQ32	Uncharacterized protein C11orf16	C11orf16	Homo sapiens (human)	0	1
Q9NQ34	Transmembrane protein 9B	TMEM9B C11orf15	Homo sapiens (human)	3	0
Q9NQ35	Nuclear receptor-interacting protein 3	NRIP3 C11orf14	Homo sapiens (human)	1	2
Q9NQ36	Signal peptide, CUB and EGF-like domain-containing protein 2	SCUBE2 CEGP1	Homo sapiens (human)	4	3
Q9NQ40	Solute carrier family 52, riboflavin transporter, member 3	SLC52A3 C20orf54 RFT2 RFVT3	Homo sapiens (human)	4	2
Q9NQ50	Large ribosomal subunit protein mL40	MRPL40 NLVCF URIM	Homo sapiens (human)	0	1
Q9NQ60	Equatorin	EQTN AFAF C9orf11	Homo sapiens (human)	2	1
Q9NQ66	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1	PLCB1 KIAA0581	Homo sapiens (human)	4	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 Chagas disease Hirschsprung's disease Kawasaki disease Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome Unverricht-Lundborg syndrome West syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult oligodendroglioma amyotrophic lateral sclerosis anaplastic astrocytoma autism spectrum disorder autistic disorder benign epilepsy with centrotemporal spikes bipolar disorder blepharospasm brain disease breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer cerebral degeneration childhood cerebral astrocytoma childhood oligodendroglioma chromosome 17p13.1 deletion syndrome colon adenocarcinoma colon cancer colonic benign neoplasm colorectal cancer coronary aneurysm coronary thrombosis cribriform carcinoma depressive disorder developmental and epileptic encephalopathy 12 developmental and epileptic encephalopathy 1 diabetes mellitus diabetic ketoacidosis early infantile epileptic encephalopathy early myoclonic encephalopathy endometriosis of uterus endometriosis epilepsy essential thrombocythemia fibrillary astrocytoma focal epilepsy focal hand dystonia gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma infertility juvenile pilocytic astrocytoma large intestine cancer lissencephaly liver cancer major depressive disorder malignant astrocytoma melancholic depression mixed glioma mixed oligodendroglioma-astrocytoma mood disorder myelodysplastic syndrome myocardial infarction myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 neuroblastoma neurotic disorder nicotine dependence obsolete infantile epileptic encephalopathy obsolete melancholia obstructive sleep apnea oligodendroglioma partial motor epilepsy pilocytic astrocytoma poikiloderma with neutropenia prediabetes syndrome primary biliary cholangitis progressive muscular atrophy protoplasmic astrocytoma schizophrenia silent myocardial infarction subependymal giant cell astrocytoma substance abuse substance-related disorder trypanosomiasis tubular adenocarcinoma visual epilepsy
Q9NQ75	Cas scaffolding protein family member 4	CASS4 C20orf32 HEFL	Homo sapiens (human)	0	1
Q9NQ76	Matrix extracellular phosphoglycoprotein	MEPE	Homo sapiens (human)	4	1
Q9NQ79	Cartilage acidic protein 1	CRTAC1 ASPIC1 CEP68	Homo sapiens (human)	7	3
Q9NQ84	G-protein coupled receptor family C group 5 member C	GPRC5C RAIG3	Homo sapiens (human)	1	0
Q9NQ88	Fructose-2,6-bisphosphatase TIGAR	TIGAR C12orf5	Homo sapiens (human)	0	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 Fanconi anemia complementation group A Fanconi anemia Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute pancreatitis adult T-cell leukemia/lymphoma adult lymphoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood leukemia childhood lymphoma chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease dementia embryoma epilepsy esophagus squamous cell carcinoma familial retinoblastoma giant cell glioblastoma glioblastoma gliosarcoma hemiplegia hepatocellular carcinoma high grade glioma hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer isolated cleft palate large intestine cancer lateral sclerosis leukemia liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma mixed glioma motor neuron disease nasopharynx carcinoma neurodegenerative disease nonpapillary renal cell carcinoma obesity obsolete ymphosarcoma pancreatitis papillary renal cell carcinoma primary cutaneous T-cell non-Hodgkin lymphoma renal carcinoma renal cell carcinoma retinoblastoma sarcomatoid renal cell carcinoma schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy stomach cancer stomach carcinoma trilateral retinoblastoma ulcerative colitis
Q9NQ90	Anoctamin-2	ANO2 C12orf3 TMEM16B	Homo sapiens (human)	7	1
Q9NQ92	Coordinator of PRMT5 and differentiation stimulator	COPRS C17orf79 COPR5	Homo sapiens (human)	0	1
Q9NQ94	APOBEC1 complementation factor	A1CF ACF ASP	Homo sapiens (human)	0	1
Q9NQA5	Transient receptor potential cation channel subfamily V member 5	TRPV5 ECAC1	Homo sapiens (human)	1	0
Q9NQC3	Reticulon-4	RTN4 KIAA0886 NOGO	Homo sapiens (human)	6	2

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