GlyCosmos Portal

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GlyConnect	April 19, 2023
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **2501 - 2525** 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
Q92540	Nonsense-mediated mRNA decay factor SMG7	SMG7 C1orf16 EST1C KIAA0250	Homo sapiens (human)	4	2
Q86US8	Telomerase-binding protein EST1A	SMG6 C17orf31 EST1A KIAA0732	Homo sapiens (human)	1	2
Q96Q15	Serine/threonine-protein kinase SMG1	SMG1 ATX KIAA0421 LIP	Homo sapiens (human)	2	2
Q9H4I9	Essential MCU regulator, mitochondrial	SMDT1 C22orf32 EMRE	Homo sapiens (human)	1	1
Q8TEV9	Guanine nucleotide exchange protein SMCR8	SMCR8	Homo sapiens (human)	3	2
A2RU48	Single-pass membrane and coiled-coil domain-containing protein 3	SMCO3 C12orf69	Homo sapiens (human)	1	1
A6NFE2	Single-pass membrane and coiled-coil domain-containing protein 2	SMCO2 C12orf70	Homo sapiens (human)	0	1
A6NHR9	Structural maintenance of chromosomes flexible hinge domain-containing protein 1	SMCHD1 KIAA0650	Homo sapiens (human)	1	1
Q96SB8	Structural maintenance of chromosomes protein 6	SMC6 SMC6L1	Homo sapiens (human)	3	2
Q8IY18	Structural maintenance of chromosomes protein 5	SMC5 KIAA0594 SMC5L1	Homo sapiens (human)	1	2
Q9NTJ3	Structural maintenance of chromosomes protein 4	SMC4 CAPC SMC4L1	Homo sapiens (human)	2	4
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
O95347	Structural maintenance of chromosomes protein 2	SMC2 CAPE SMC2L1	Homo sapiens (human)	6	1
Q8NDV3	Structural maintenance of chromosomes protein 1B	SMC1B SMC1L2	Homo sapiens (human)	1	1
Q14683	Structural maintenance of chromosomes protein 1A	SMC1A DXS423E KIAA0178 SB1.8 SMC1 SMC1L1	Homo sapiens (human)	3	2
Q96JZ5	Transmembrane 9 superfamily member	SMBP	Homo sapiens (human)	1	0
Q969G3	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1	SMARCE1 BAF57	Homo sapiens (human)	0	1
Q6STE5	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3	SMARCD3 BAF60C	Homo sapiens (human)	0	1
Q92925	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 2	SMARCD2 BAF60B	Homo sapiens (human)	1	2
Q96GM5	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 1	SMARCD1 BAF60A	Homo sapiens (human)	1	1
Q8TAQ2	SWI/SNF complex subunit SMARCC2	SMARCC2 BAF170	Homo sapiens (human)	0	1
Q92922	SWI/SNF complex subunit SMARCC1	SMARCC1 BAF155	Homo sapiens (human)	3	3
Q12824	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1	SMARCB1 BAF47 INI1 SNF5L1	Homo sapiens (human)	1	1
Q9NZC9	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1	SMARCAL1 HARP	Homo sapiens (human)	2	3
Q9H4L7	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1	SMARCAD1 KIAA1122	Homo sapiens (human)	0	1

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