GlyCosmos Portal

Displaying entries **701 - 725** of **18496** in total

« First

‹ Prev

…

25

26

27

28

29

30

31

32

33

…

Next ›

Last »
UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9Y226	Solute carrier family 22 member 13	SLC22A13 OCTL1 ORCTL3	4	1
Q9Y224	RNA transcription, translation and transport factor protein	RTRAF C14orf166	0	1
Q9Y219	Protein jagged-2	JAG2	5	0
Q9Y217	Myotubularin-related protein 6	MTMR6	3	2	cancer
Q9Y210	Short transient receptor potential channel 6	TRPC6 TRP6	5	5
Q9WJR5	Endogenous retrovirus group K member 19 Pol protein	ERVK-19	1	1
Q9UQV4	Lysosome-associated membrane glycoprotein 3	LAMP3 DCLAMP TSC403	9	6
Q9UQR1	Zinc finger protein 148	ZNF148 ZBP89	8	1
Q9UQR0	Sex comb on midleg-like protein 2	SCML2	4	1
Q9UQQ1	Aminopeptidase NAALADL1	NAALADL1 NAALADASEL NAALADL	7	0
Q9UQP3	Tenascin-N	TNN TNW	4	15
Q9UQN3	Charged multivesicular body protein 2b	CHMP2B	1	1
Q9UQM7	Calcium/calmodulin-dependent protein kinase type II subunit alpha	CAMK2A CAMKA KIAA0968	1	1
Q9UQK1	Protein phosphatase 1 regulatory subunit 3C	PPP1R3C PPP1R5	0	1	antithrombin III deficiency breast cancer cancer colorectal cancer colorectal carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma head and neck cancer hepatocellular carcinoma large intestine cancer liver cancer major depressive disorder melancholic depression neurotic disorder obsolete melancholia post-traumatic stress disorder protein C deficiency protein S deficiency steatotic liver disease thrombophilia type 2 diabetes mellitus
Q9UQF2	C-Jun-amino-terminal kinase-interacting protein 1	MAPK8IP1 IB1 JIP1 PRKM8IP	1	1
Q9UQF0	Syncytin-1	ERVW-1 ERVWE1	7	0
Q9UQE7	Structural maintenance of chromosomes protein 3	SMC3 BAM BMH CSPG6 SMC3L1	2	1	Burkitt lymphoma Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome 2 Cornelia de Lange syndrome 3 Cornelia de Lange syndrome Dubowitz syndrome Laron syndrome Marfan syndrome Meckel syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Peters anomaly Prader-Willi syndrome Roberts syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Turner syndrome X-linked Aarskog syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adult lymphoma allergic asthma anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis 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 attention deficit hyperactivity disorder atypical chronic myeloid leukemia, BCR-ABL1 negative autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome blepharitis blind hypotensive eye bone cancer bone osteosarcoma bronchus cancer bronchus carcinoma cancer carcinoma cataract 32 multiple types cataract central nervous system lymphoma childhood lymphoma choanal atresia chondrodysplasia-pseudohermaphroditism syndrome chronic interstitial cystitis chronic monocytic leukemia cleft palate cleidocranial dysplasia clubfoot colon carcinoma colorectal cancer cone-rod dystrophy congenital diaphragmatic hernia congenital nystagmus congenital ptosis cornea plana coronary artery disease craniosynostosis cribriform carcinoma cryptorchidism dissociated nystagmus embryoma epilepsy esophagitis fundus albipunctatus gastroesophageal reflux disease generalized anxiety disorder gingivitis glaucoma gonadal dysgenesis granular cell carcinoma hepatocellular carcinoma humeroradial synostosis hydrocephalus hypertrichosis hypertropia hypospadias inguinal hernia intellectual disability interstitial cystitis intestinal benign neoplasm intestinal cancer intestinal volvulus intrinsic asthma isolated cleft palate kidney failure kwashiorkor large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoid leukemia lymphoma marasmus mechanical strabismus megacolon microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly myeloid leukemia myopia neuropathy nutrition disease obsolete SC phocomelia syndrome obsolete ymphosarcoma ophthalmoplegia osteosarcoma patent foramen ovale pathologic nystagmus peptic esophagitis periodontitis peripheral nervous system disease placental insufficiency pneumonia prostate cancer prostate carcinoma protein-energy malnutrition prune belly syndrome ptosis pulmonary valve stenosis pyloric stenosis radioulnar synostosis retinitis pigmentosa sarcomatoid carcinoma sensorineural hearing loss situs inversus speech disorder spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 thromboangiitis obliterans toxic megacolon trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis tubular adenocarcinoma ventricular septal defect vesicoureteral reflux visual epilepsy
Q9UQD0	Sodium channel protein type 8 subunit alpha	SCN8A MED	8	1
Q9UQC9	Calcium-activated chloride channel regulator 2	CLCA2 CACC3	10	13
Q9UQB8	BAR/IMD domain-containing adapter protein 2	BAIAP2	1	4
Q9UQB3	Catenin delta-2	CTNND2 NPRAP	13	1
Q9UQ90	Mitochondrial inner membrane m-AAA protease component paraplegin	SPG7 CAR CMAR PGN	0	1
Q9UQ88	Cyclin-dependent kinase 11A	CDK11A CDC2L2 CDC2L3 PITSLREB	1	1
Q9UQ84	Exonuclease 1	EXO1 EXOI HEX1	2	1
Q9UQ80	Proliferation-associated protein 2G4	PA2G4 EBP1	1	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements