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 **124201 - 124225** of **126547** in total

« First

‹ Prev

…

4965

4966

4967

4968

4969

4970

4971

4972

4973

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P19221	Prothrombin	F2 Cf2	Mus musculus (house mouse)	4	4
Q8VE98	CD276 antigen	Cd276 B7h3	Mus musculus (house mouse)	4	4
Q6MZW2	Follistatin-related protein 4	FSTL4 KIAA1061	Homo sapiens (human)	8	4
O94910	Adhesion G protein-coupled receptor L1	ADGRL1 KIAA0821 LEC2 LPHN1	Homo sapiens (human)	9	4
Q8IW45	ATP-dependent (S)-NAD(P)H-hydrate dehydratase	NAXD CARKD	Homo sapiens (human)	2	4
Q8NBI5	Equilibrative nucleobase transporter 1	SLC43A3 ENBT1	Homo sapiens (human)	4	4
Q15596	Nuclear receptor coactivator 2	NCOA2 BHLHE75 SRC2 TIF2	Homo sapiens (human)	3	4
P98153	Integral membrane protein DGCR2/IDD	DGCR2 IDD KIAA0163	Homo sapiens (human)	2	4	Bannayan-Riley-Ruvalcaba syndrome Baraitser-Winter syndrome Cowden syndrome DiGeorge syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Nezelof syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia acromegaly acute myocardial infarction adrenal gland cancer amyloidosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bipolar disorder blepharophimosis branchiootic syndrome cancer cervix disease chronic interstitial cystitis congenital heart disease coronary thrombosis craniosynostosis degenerative disc disease delusional disorder diabetes mellitus diabetic ketoacidosis double outlet right ventricle duodenum cancer embryoma epilepsy heart cancer hyperpituitarism hypoparathyroidism-deafness-renal disease syndrome hypoparathyroidism immune system disease intellectual disability interstitial cystitis learning disability microcephaly myocardial infarction myotonic dystrophy type 1 neuroblastoma obsolete type 1 diabetes mellitus 9 orofaciodigital syndrome I orofaciodigital syndrome X osteoporosis paranoid schizophrenia pheochromocytoma primary biliary cholangitis prune belly syndrome pseudohypoparathyroidism schizophrenia silent myocardial infarction small intestine cancer type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus velocardiofacial syndrome ventricular septal defect visual epilepsy
O14976	Cyclin-G-associated kinase	GAK DNAJC26	Homo sapiens (human)	3	4
Q3UMW8	Bis(monoacylglycero)phosphate synthase CLN5	Cln5 Bmps	Mus musculus (house mouse)	7	4
Q8BYR5	Calcium-dependent secretion activator 2	Cadps2 Caps2	Mus musculus (house mouse)	4	4
P17405	Sphingomyelin phosphodiesterase	SMPD1 ASM	Homo sapiens (human)	8	4	Alzheimer's disease Chagas disease Evans' syndrome Fabry disease Gaucher's disease Laron syndrome Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wilson disease achondroplasia acute myocardial infarction acute promyelocytic leukemia adrenal gland cancer adult fibrosarcoma adult respiratory distress syndrome aggressive systemic mastocytosis alcohol dependence alcohol use disorder alcoholic hepatitis allergic asthma alternating hemiplegia of childhood amnestic disorder antithrombin III deficiency anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autoimmune thrombocytopenic purpura autonomic neuropathy bacterial sepsis bipolar disorder botryoid rhabdomyosarcoma cancer cataract 32 multiple types central nervous system cancer central nervous system disease cerebral infarction cerebrovascular disease cholecystolithiasis choledocholithiasis cholelithiasis chronic fatigue syndrome chronic obstructive pulmonary disease chylomicron retention disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis cystic fibrosis depressive disorder diabetes mellitus diabetic angiopathy diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy disease of mental health disease of metabolism dissociated nystagmus duodenum cancer dysthymic disorder embryoma embryonal rhabdomyosarcoma encephalitis encephalomyelitis familial adenomatous polyposis 1 familial adenomatous polyposis fibrosarcoma gastroenteritis generalized anxiety disorder gliosarcoma head and neck squamous cell carcinoma heart cancer hemochromatosis hepatitis hepatocellular carcinoma herpes simplex high grade glioma hyperhomocysteinemia hypersplenism ileitis ileocolitis indolent systemic mastocytosis inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease intrinsic asthma iron metabolism disease islet cell tumor kwashiorkor large intestine cancer late onset Parkinson's disease lipid storage disease liver cancer liver carcinoma liver cirrhosis lung cancer lung non-small cell carcinoma lysosomal storage disease major depressive disorder marasmus mast-cell leukemia mastocytosis melancholic depression melanoma metachromatic leukodystrophy microcytic anemia mixed glioma multiple myeloma multiple sclerosis myelitis myocardial infarction nasopharynx carcinoma nervous system disease neuronal ceroid lipofuscinosis 6A neuropathy neurotic disorder newborn respiratory distress syndrome nutmeg liver nutrition disease obesity obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia osteoporosis ovarian cancer ovarian carcinoma pathologic nystagmus periodontal disease peripheral nervous system disease pheochromocytoma pneumonia prostate cancer prostate carcinoma protein C deficiency protein S deficiency protein-energy malnutrition psychotic disorder respiratory syncytial virus infectious disease retrograde amnesia rheumatoid arthritis sea-blue histiocytosis sickle cell anemia silent myocardial infarction skin melanoma small intestine cancer sphingolipidosis splenic disease splenic infarction spontaneous ocular nystagmus steatotic liver disease systemic lupus erythematosus systemic mastocytosis thrombophilia trypanosomiasis tuberculosis type 2 diabetes mellitus ulcerative colitis urinary bladder cancer viral infectious disease xanthomatosis
Q9P0T7	Proton-transporting V-type ATPase complex assembly regulator TMEM9	TMEM9 DERP4 TMEM9A	Homo sapiens (human)	6	4
E9PZP8	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	Herc1	Mus musculus (house mouse)	4	4
Q15365	Poly(rC)-binding protein 1	PCBP1	Homo sapiens (human)	9	4
Q9NYQ7	Cadherin EGF LAG seven-pass G-type receptor 3	CELSR3 CDHF11 EGFL1 FMI1 KIAA0812 MEGF2	Homo sapiens (human)	20	4
Q15652	Probable JmjC domain-containing histone demethylation protein 2C	JMJD1C JHDM2C KIAA1380 TRIP8	Homo sapiens (human)	41	4
O95158	Neurexophilin-4	NXPH4 NPH4	Homo sapiens (human)	4	4
E9Q8I0	Complement component factor h	Cfh	Mus musculus (house mouse)	6	4
A8K2U0	Alpha-2-macroglobulin-like protein 1	A2ML1 CPAMD9	Homo sapiens (human)	6	4
Q9P244	Leucine-rich repeat and fibronectin type III domain-containing protein 1	LRFN1 KIAA1484 SALM2	Homo sapiens (human)	4	4
Q925J9	Mediator of RNA polymerase II transcription subunit 1	Med1 Crsp210 Drip205 Pbp Pparbp Trap220 Trip2	Mus musculus (house mouse)	4	4
Q80WQ6	Inactive rhomboid protein 2	Rhbdf2 Irhom2 Rhbdl6 Rhor	Mus musculus (house mouse)	3	4
Q16790	Carbonic anhydrase 9	CA9 G250 MN	Homo sapiens (human)	2	4
P35658	Nuclear pore complex protein Nup214	NUP214 CAIN CAN KIAA0023	Homo sapiens (human)	219	4

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements