GlyCosmos Portal

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GlyConnect	April 19, 2023
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The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **118726 - 118750** 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
Q96FX7	tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit TRMT61A	TRMT61A C14orf172 TRM61	Homo sapiens (human)	0	1
Q60634	Flotillin-2	Flot2 Esa1 M17s1	Mus musculus (house mouse)	0	1
Q9GZR7	ATP-dependent RNA helicase DDX24	DDX24	Homo sapiens (human)	2	1
Q9NZK7	Group IIE secretory phospholipase A2	PLA2G2E	Homo sapiens (human)	1	1	atopic dermatitis benign mastocytoma dermatitis extracutaneous mastocytoma indolent systemic mastocytosis mast cell neoplasm mastocytosis obesity
Q15633	RISC-loading complex subunit TARBP2	TARBP2 TRBP	Homo sapiens (human)	0	1
V5DQM2	Aldehyde dehydrogenase	TCDM_01424	Trypanosoma cruzi Dm28c	0	1
P41235	Hepatocyte nuclear factor 4-alpha	HNF4A HNF4 NR2A1 TCF14	Homo sapiens (human)	0	1
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
Q8WVH0	Complexin-3	CPLX3	Homo sapiens (human)	0	1
E9PZ00	Prosaposin	Psap	Mus musculus (house mouse)	4	1
P35321	Cornifin-A	SPRR1A	Homo sapiens (human)	0	1
Q9NRX2	Large ribosomal subunit protein bL17m	MRPL17 LIP2	Homo sapiens (human)	0	1
P21917	D(4) dopamine receptor	DRD4	Homo sapiens (human)	4	1
A0A1B0GUW6	Uncharacterized protein SPEM3	SPEM3	Homo sapiens (human)	0	1
V5BJY2	RanBP2-type domain-containing protein	TCDM_03227	Trypanosoma cruzi Dm28c	0	1
Q8TDN2	Potassium voltage-gated channel subfamily V member 2	KCNV2	Homo sapiens (human)	3	1
Q9D051	Pyruvate dehydrogenase E1 component subunit beta, mitochondrial	Pdhb	Mus musculus (house mouse)	0	1
Q6ICG6	Uncharacterized protein KIAA0930	KIAA0930 C22orf9	Homo sapiens (human)	3	1
A4D2G3	Olfactory receptor 2A25	OR2A25 OR2A25P OR2A27	Homo sapiens (human)	1	1
Q9ER74	Sal-like protein 1	Sall1 Sal3	Mus musculus (house mouse)	7	1
Q4DC65	GRIP domain-containing protein	Tc00.1047053506777.110	Trypanosoma cruzi strain CL Brener	0	1
P62867	Small ribosomal subunit protein eS30	Fau	Mus spicilegus (steppe mouse)	0	1
V5BD50	Uncharacterized protein	TCDM_08028	Trypanosoma cruzi Dm28c	0	1
O35654	DNA polymerase delta subunit 2	Pold2	Mus musculus (house mouse)	3	1
Q9ESW4	Acylglycerol kinase, mitochondrial	Agk Mulk	Mus musculus (house mouse)	0	1

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