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 **118626 - 118650** 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
O75150	E3 ubiquitin-protein ligase BRE1B	RNF40 BRE1B KIAA0661	Homo sapiens (human)	1	1
Q6ZQE4	Nuclear envelope integral membrane protein 1	Nemp1 Kiaa0286 Tmem194 Tmem194a	Mus musculus (house mouse)	1	1
P32570	Mediator of RNA polymerase II transcription subunit 22	SRB6 MED22	Saccharomyces cerevisiae S288C	1	1
Q4E4N8	Secretory carrier-associated membrane protein	Tc00.1047053506925.100	Trypanosoma cruzi strain CL Brener	0	1
O94854	Microtubule-actin cross-linking factor 1, isoforms 6/7	MACF1 KIAA0754	Homo sapiens (human)	0	1
M7ZJP3	Tetratricopeptide repeat protein 7B	TRIUR3_19169	Triticum urartu	0	1
P0C617	Olfactory receptor 5AL1	OR5AL1 OR5AL1P	Homo sapiens (human)	1	1
Q14003	Potassium voltage-gated channel subfamily C member 3	KCNC3	Homo sapiens (human)	3	1
P09497	Clathrin light chain B	CLTB	Homo sapiens (human)	0	1
Q8NDZ4	Divergent protein kinase domain 2A	DIPK2A C3orf58 DIA1	Homo sapiens (human)	1	1
Q9CAJ9	BTB/POZ domain-containing protein At1g63850	At1g63850	Arabidopsis thaliana (thale cress)	0	1
Q9DBY8	Nuclear valosin-containing protein-like	Nvl	Mus musculus (house mouse)	0	1
Q8TD06	Anterior gradient protein 3	AGR3 BCMP11 PDIA18	Homo sapiens (human)	3	1
V4Z8Z4	Putative vacuolar protein sorting-associated protein 26	TGVEG_263500	Toxoplasma gondii VEG	0	1
Q641P0	Actin-related protein 3B	Actr3b	Mus musculus (house mouse)	0	1
P06241	Tyrosine-protein kinase Fyn	FYN	Homo sapiens (human)	0	1
Q13416	Origin recognition complex subunit 2	ORC2 ORC2L	Homo sapiens (human)	2	1
Q03426	Mevalonate kinase	MVK	Homo sapiens (human)	1	1
Q9Y6G3	Large ribosomal subunit protein mL42	MRPL42 MRPL31 MRPS32 RPML31	Homo sapiens (human)	0	1
V5B0Q8	Hexosyltransferase	TCDM_11325	Trypanosoma cruzi Dm28c	0	1
P32873	GTPase-activating protein BEM3	BEM3	Saccharomyces cerevisiae S288C	13	1
P00558	Phosphoglycerate kinase 1	PGK1 PGKA	Homo sapiens (human)	6	1	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Gilbert syndrome Kawasaki disease Menkes disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wiskott-Aldrich syndrome X-linked cleft palate with or without ankyloglossia X-linked distal spinal muscular atrophy 3 X-linked dystonia-parkinsonism X-linked severe combined immunodeficiency adenosquamous carcinoma agenesis of the corpus callosum with peripheral neuropathy amyotrophic lateral sclerosis anaplastic astrocytoma anemia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome bilirubin metabolic disorder blindness brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer childhood cerebral astrocytoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined T cell and B cell immunodeficiency congestive heart failure cystinuria embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endomyocardial fibrosis epilepsy esophageal cancer esophageal carcinoma essential thrombocythemia familial periodic paralysis fibrillary astrocytoma fundus dystrophy galactosemia gallbladder cancer gallbladder carcinoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hereditary spherocytosis high grade glioma hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia intellectual disability juvenile pilocytic astrocytoma kidney failure large intestine cancer learning disability liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus macrocytic anemia malignant astrocytoma melanoma microphthalmia migraine mixed glioma motor peripheral neuropathy myelodysplastic syndrome myoglobinuria myopathy neuroblastoma nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum occipital horn syndrome ovarian cancer ovarian carcinoma oxyphilic adenoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma pilocytic astrocytoma progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma pseudosarcomatous fibromatosis pulmonary large cell neuroendocrine carcinoma pure red-cell aplasia renal carcinoma renal cell carcinoma retinitis pigmentosa 10 rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia skin melanoma spinal muscular atrophy stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic lupus erythematosus thyroid gland papillary carcinoma uterine corpus cancer visual epilepsy
Q5W0V3	FHF complex subunit HOOK interacting protein 2A	FHIP2A FAM160B1 KIAA1600	Homo sapiens (human)	0	1
Q14123	Dual specificity calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1C	PDE1C	Homo sapiens (human)	0	1
Q9Z0H7	B-cell lymphoma/leukemia 10	Bcl10 Ciper Clap	Mus musculus (house mouse)	0	1

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