GlyCosmos Portal

Source	Last Updated
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 **1501 - 1525** 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
Q9NR12	PDZ and LIM domain protein 7	PDLIM7 ENIGMA	Homo sapiens (human)	13	4
Q7LGC8	Carbohydrate sulfotransferase 3	CHST3	Homo sapiens (human)	6	4	Bannayan-Riley-Ruvalcaba syndrome Bartter disease Conn's syndrome Cowden syndrome Desbuquois dysplasia Hailey-Hailey disease Laron syndrome Larsen syndrome Larsen-like syndrome B3GAT3 type Ollier disease Rothmund-Thomson syndrome SOST-related sclerosing bone dysplasia Schwartz-Jampel syndrome 1 Silverman-Handmaker type dyssegmental dysplasia Sjogren's syndrome Waterhouse-Friderichsen syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia acute promyelocytic leukemia adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adrenoleukodystrophy adult fibrosarcoma agnosia alcoholic hepatitis alcoholic liver cirrhosis amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve insufficiency aortic valve stenosis apparent mineralocorticoid excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis 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 atrophy of testis autoimmune hepatitis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease blastomycosis breast cancer breast carcinoma buphthalmos cancer cardiomyopathy cardiovascular system disease choriocarcinoma cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital adrenal hyperplasia coronary artery disease craniosynostosis cutis laxa cystadenoma dermatitis developmental coordination disorder diabetes mellitus diabetic ketoacidosis diastrophic dysplasia embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis enterocele esotropia essential hypertension fibrosarcoma follicular adenoma heart disease hepatitis hereditary multiple exostoses humeroradial synostosis hydrocephalus hydrophthalmos hyperopia hypertension hypertrophic cardiomyopathy hypogonadotropic hypogonadism 23 with or without anosmia inclusion body myositis intrahepatic cholestasis isolated cleft palate juvenile glaucoma keratoconjunctivitis sicca leiomyoma liver cirrhosis lung small cell carcinoma mal de Meleda microcystic adenoma mitral valve insufficiency mitral valve prolapse mitral valve stenosis monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia myofibroma neurogenic arthropathy obesity obsolete type 1 diabetes mellitus 9 obstructive hydrocephalus osteochondrodysplasia osteoporosis ovarian cancer ovarian carcinoma ovarian hyperstimulation syndrome papillary adenoma paracoccidioidomycosis patent foramen ovale placenta cancer polycystic ovary syndrome postural orthostatic tachycardia syndrome primary hyperaldosteronism primary pulmonary hypertension progressive familial intrahepatic cholestasis progressive pseudorheumatoid arthropathy of childhood pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss spondyloepiphyseal dysplasia congenita spondyloepiphyseal dysplasia with congenital joint dislocations strabismic amblyopia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tricuspid valve insufficiency tricuspid valve stenosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uterine corpus cancer uterine fibroid varicose veins ventricular septal defect
P09429	High mobility group protein B1	HMGB1 HMG1	Homo sapiens (human)	5	4
P05787	Keratin, type II cytoskeletal 8	KRT8 CYK8	Homo sapiens (human)	22	4
O75446	Histone deacetylase complex subunit SAP30	SAP30	Homo sapiens (human)	2	4
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
Q96HC4	PDZ and LIM domain protein 5	PDLIM5 ENH	Homo sapiens (human)	30	4
Q7Z6E9	E3 ubiquitin-protein ligase RBBP6	RBBP6 P2PR PACT RBQ1	Homo sapiens (human)	12	4
Q9H9K5	Endogenous retroviral envelope protein HEMO	ERVMER34-1 HEMO	Homo sapiens (human)	11	4
Q8N139	ATP-binding cassette sub-family A member 6	ABCA6	Homo sapiens (human)	6	4
Q01668	Voltage-dependent L-type calcium channel subunit alpha-1D	CACNA1D CACH3 CACN4 CACNL1A2 CCHL1A2	Homo sapiens (human)	6	4
Q96NU0	Contactin-associated protein-like 3B	CNTNAP3B CASPR3B	Homo sapiens (human)	4	4
Q6UWY0	Arylsulfatase K	ARSK TSULF	Homo sapiens (human)	7	4	lysosomal storage disease
Q96DZ1	Endoplasmic reticulum lectin 1	ERLEC1 C2orf30 XTP3TPB	Homo sapiens (human)	4	4	anorexia nervosa bronchus cancer bronchus carcinoma cancer cholestasis lung benign neoplasm lung cancer lung carcinoma spinal cord disease syringomyelia
Q9NTU7	Cerebellin-4	CBLN4 CBLNL1	Homo sapiens (human)	2	4
P19021	Peptidyl-glycine alpha-amidating monooxygenase	PAM	Homo sapiens (human)	13	4
P21453	Sphingosine 1-phosphate receptor 1	S1PR1 CHEDG1 EDG1	Homo sapiens (human)	5	4
P47972	Neuronal pentraxin-2	NPTX2	Homo sapiens (human)	3	4
O14513	Nck-associated protein 5	NCKAP5 ERIH NAP5	Homo sapiens (human)	6	4
Q6ZQN7	Solute carrier organic anion transporter family member 4C1	SLCO4C1 OATP4C1 OATPX SLC21A20	Homo sapiens (human)	2	4
Q9NTJ3	Structural maintenance of chromosomes protein 4	SMC4 CAPC SMC4L1	Homo sapiens (human)	2	4
Q14596	Next to BRCA1 gene 1 protein	NBR1 1A13B KIAA0049 M17S2	Homo sapiens (human)	0	4
Q7L1W4	Volume-regulated anion channel subunit LRRC8D	LRRC8D LRRC5	Homo sapiens (human)	10	4
P25054	Adenomatous polyposis coli protein	APC DP2.5	Homo sapiens (human)	7	4
Q0VF96	Cingulin-like protein 1	CGNL1 JACOP KIAA1749	Homo sapiens (human)	1	4

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