GlyCosmos Portal

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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 **2826 - 2850** 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
Q8TDD5	Mucolipin-3	MCOLN3	Homo sapiens (human)	4	4
E7ETB4	Clusterin (Fragment)	CLU	Homo sapiens (human)	4	0
Q9Y5E3	Protocadherin beta-6	PCDHB6	Homo sapiens (human)	4	0
O76094	Signal recognition particle subunit SRP72	SRP72	Homo sapiens (human)	4	3
J3KTH9	Angiotensin-converting enzyme	ACE	Homo sapiens (human)	4	0
Q15056	Eukaryotic translation initiation factor 4H	EIF4H KIAA0038 WBSCR1 WSCR1	Homo sapiens (human)	4	1
Q9H1V8	Sodium-dependent neutral amino acid transporter SLC6A17	SLC6A17 NTT4	Homo sapiens (human)	4	3
P20700	Lamin-B1	LMNB1 LMN2 LMNB	Homo sapiens (human)	4	3
Q96KV6	Putative butyrophilin subfamily 2 member A3	BTN2A3P BTN2A3	Homo sapiens (human)	4	0
Q9H3S1	Semaphorin-4A	SEMA4A SEMAB SEMB	Homo sapiens (human)	4	7
P05060	Secretogranin-1	CHGB SCG1	Homo sapiens (human)	4	2
Q9BYC5	Alpha-(1,6)-fucosyltransferase	FUT8	Homo sapiens (human)	4	1	Laron syndrome achondroplasia adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma buphthalmos cancer chronic fatigue syndrome chronic myeloid leukemia chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congenital disorder of glycosylation coronary artery disease embryoma encephalitis encephalomyelitis epilepsy follicular adenoma glaucoma hepatitis A hepatitis C hepatitis hepatocellular carcinoma hydrophthalmos idiopathic interstitial pneumonia intellectual disability juvenile glaucoma large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma microcephaly microcystic adenoma myelitis ovarian cancer ovarian carcinoma pancreatic ductal adenocarcinoma pancreatic intraductal papillary-mucinous neoplasm papillary adenoma papillary carcinoma placental insufficiency polyhydramnios postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pseudomyxoma peritonei pulmonary emphysema pulmonary fibrosis schizophrenia scoliosis skin melanoma visual epilepsy
O75534	Cold shock domain-containing protein E1	CSDE1 D1S155E KIAA0885 NRU UNR	Homo sapiens (human)	4	2
O00584	Ribonuclease T2	RNASET2 RNASE6PL	Homo sapiens (human)	4	24
P51689	Arylsulfatase D	ARSD	Homo sapiens (human)	4	10	Asperger syndrome Bannayan-Riley-Ruvalcaba syndrome Beckwith-Wiedemann syndrome CLOVES syndrome Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Cowden syndrome Down syndrome Dubowitz syndrome Lown-Ganong-Levine syndrome Marfan syndrome Mowat-Wilson 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 Perlman syndrome Prader-Willi syndrome Rett syndrome Richter's syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Sotos syndrome Williams-Beuren syndrome Wolff-Parkinson-White syndrome X-linked Aarskog syndrome acute kidney tubular necrosis acute myeloid leukemia acute promyelocytic leukemia adult respiratory distress syndrome alexia amnestic disorder aniridia anxiety disorder aortic valve disease 1 aortic valve disease 2 aortic valve stenosis argininosuccinic aciduria arteriosclerotic cardiovascular disease 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 atrioventricular block atrioventricular septal defect attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bicuspid aortic valve disease breast cancer breast carcinoma buphthalmos cardiomyopathy cardiovascular system disease cerebral palsy chondrodysplasia-pseudohermaphroditism syndrome chronic lymphocytic leukemia citrullinemia communication disorder conduct disorder congenital heart disease congestive heart failure coronary artery disease depressive disorder developmental coordination disorder disease of mental health dyslexia dysthymic disorder eating disorder endocarditis endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy essential hypertension excessive tearing familial hypertrophic cardiomyopathy fragile X syndrome generalized anxiety disorder glaucoma heart disease hemiplegia hydrophthalmos hyperargininemia hypertension hypertrophic cardiomyopathy hypospadias immune system disease infective endocarditis intellectual disability juvenile glaucoma lacrimal apparatus disease language disorder learning disability major depressive disorder melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia neurotic disorder newborn respiratory distress syndrome nicotine dependence obesity obsolete melancholia patent ductus arteriosus patent foramen ovale phobic disorder polycystic ovary syndrome post-traumatic stress disorder primary open angle glaucoma psychotic disorder pulmonary valve stenosis retrograde amnesia schizophrenia sclerocornea situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy subacute bacterial endocarditis substance abuse substance-related disorder supravalvular aortic stenosis syndromic X-linked intellectual disability 94 tuberous sclerosis ventricular septal defect visual epilepsy
Q9H5Y7	SLIT and NTRK-like protein 6	SLITRK6	Homo sapiens (human)	4	1
Q16602	Calcitonin gene-related peptide type 1 receptor	CALCRL CGRPR	Homo sapiens (human)	4	18
G3XAM2	Complement factor I	CFI	Homo sapiens (human)	4	0
Q9BWF2	E3 ubiquitin-protein ligase TRAIP	TRAIP RNF206 TRIP	Homo sapiens (human)	4	3
P42857	Neuronal vesicle trafficking-associated protein 1	NSG1 D4S234 NEEP21	Homo sapiens (human)	4	1
Q9UPW6	DNA-binding protein SATB2	SATB2 KIAA1034	Homo sapiens (human)	4	3
Q9BQ16	Testican-3	SPOCK3 TICN3	Homo sapiens (human)	4	1
Q5VUB5	Protein FAM171A1	FAM171A1 APCN C10orf38	Homo sapiens (human)	4	1
P36578	Large ribosomal subunit protein uL4	RPL4 RPL1	Homo sapiens (human)	4	3
Q9Y5E7	Protocadherin beta-2	PCDHB2	Homo sapiens (human)	4	1

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