GlyCosmos Portal

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Displaying entries **6251 - 6275** 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
Q9UQV4	Lysosome-associated membrane glycoprotein 3	LAMP3 DCLAMP TSC403	Homo sapiens (human)	9	6
Q9UQR1	Zinc finger protein 148	ZNF148 ZBP89	Homo sapiens (human)	8	1
Q9UQR0	Sex comb on midleg-like protein 2	SCML2	Homo sapiens (human)	4	1
Q9UQQ1	Aminopeptidase NAALADL1	NAALADL1 NAALADASEL NAALADL	Homo sapiens (human)	7	0
Q9UQP3	Tenascin-N	TNN TNW	Homo sapiens (human)	4	15
Q9UQN3	Charged multivesicular body protein 2b	CHMP2B	Homo sapiens (human)	1	1
Q9UQM7	Calcium/calmodulin-dependent protein kinase type II subunit alpha	CAMK2A CAMKA KIAA0968	Homo sapiens (human)	1	1
Q9UQK1	Protein phosphatase 1 regulatory subunit 3C	PPP1R3C PPP1R5	Homo sapiens (human)	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	Homo sapiens (human)	1	1
Q9UQF0	Syncytin-1	ERVW-1 ERVWE1	Homo sapiens (human)	7	0
Q9UQE7	Structural maintenance of chromosomes protein 3	SMC3 BAM BMH CSPG6 SMC3L1	Homo sapiens (human)	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	Homo sapiens (human)	8	1
Q9UQC9	Calcium-activated chloride channel regulator 2	CLCA2 CACC3	Homo sapiens (human)	10	13
Q9UQB8	BAR/IMD domain-containing adapter protein 2	BAIAP2	Homo sapiens (human)	1	4
Q9UQB3	Catenin delta-2	CTNND2 NPRAP	Homo sapiens (human)	13	1
Q9UQ90	Mitochondrial inner membrane m-AAA protease component paraplegin	SPG7 CAR CMAR PGN	Homo sapiens (human)	0	1
Q9UQ88	Cyclin-dependent kinase 11A	CDK11A CDC2L2 CDC2L3 PITSLREB	Homo sapiens (human)	1	1
Q9UQ84	Exonuclease 1	EXO1 EXOI HEX1	Homo sapiens (human)	2	1
Q9UQ80	Proliferation-associated protein 2G4	PA2G4 EBP1	Homo sapiens (human)	1	1
Q9UQ74	Pregnancy-specific beta-1-glycoprotein 8	PSG8	Homo sapiens (human)	7	0
Q9UQ72	Pregnancy-specific beta-1-glycoprotein 11	PSG11 PSG13 PSG14	Homo sapiens (human)	4	1
Q9UQ53	Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B	MGAT4B	Homo sapiens (human)	6	3	cancer depressive disorder embryoma major depressive disorder melancholic depression obsolete melancholia
Q9UQ52	Contactin-6	CNTN6	Homo sapiens (human)	14	4	Gilles de la Tourette syndrome Hirschsprung's disease Parkinson's disease 2 acquired immunodeficiency syndrome adenoid cystic carcinoma alcohol dependence alcohol use disorder anorexia nervosa attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder breast cancer communicating hydrocephalus cone-rod dystrophy 2 cone-rod dystrophy differentiated thyroid gland carcinoma epilepsy hydrocephalus intellectual disability learning disability obstructive hydrocephalus ovarian carcinoma salivary gland adenoid cystic carcinoma schizophrenia senile degeneration of brain systemic lupus erythematosus
Q9UQ35	Serine/arginine repetitive matrix protein 2	SRRM2 KIAA0324 SRL300 SRM300	Homo sapiens (human)	46	2
Q9UQ26	Regulating synaptic membrane exocytosis protein 2	RIMS2 KIAA0751 RAB3IP3 RIM2	Homo sapiens (human)	2	2

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