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 **14151 - 14175** of **18496** in total

« First

‹ Prev

…

563

564

565

566

567

568

569

570

571

…

Next ›

Last »
UniProt ID	Protein Name ▼	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9BZE4	GTP-binding protein 4	GTPBP4 CRFG NOG1	Homo sapiens (human)	1	1
A4D1E9	GTP-binding protein 10	GTPBP10 OBGH2	Homo sapiens (human)	0	1
O00178	GTP-binding protein 1	GTPBP1	Homo sapiens (human)	3	2
P62826	GTP-binding nuclear protein Ran	RAN ARA24	Homo sapiens (human)	0	1
Q9H4S2	GS homeobox 1	GSX1 GSH1	Homo sapiens (human)	1	1
Q4V328	GRIP1-associated protein 1	GRIPAP1 KIAA1167	Homo sapiens (human)	1	1
Q8IWJ2	GRIP and coiled-coil domain-containing protein 2	GCC2 KIAA0336 RANBP2L4	Homo sapiens (human)	0	1
Q9C091	GREB1-like protein	GREB1L C18orf6 KIAA1772	Homo sapiens (human)	0	1
Q2WGN9	GRB2-associated-binding protein 4	GAB4	Homo sapiens (human)	1	2
Q13480	GRB2-associated-binding protein 1	GAB1	Homo sapiens (human)	2	1
Q6Y7W6	GRB10-interacting GYF protein 2	GIGYF2 KIAA0642 PERQ2 TNRC15	Homo sapiens (human)	8	2
O75420	GRB10-interacting GYF protein 1	GIGYF1 CDS2 PERQ1	Homo sapiens (human)	2	1
B7ZL93	GPR107 protein (Fragment)	GPR107	Homo sapiens (human)	1	0
Q9UHW5	GPN-loop GTPase 3	GPN3 ATPBD1C	Homo sapiens (human)	0	1
P52961	GPI-linked NAD(P)(+)--arginine ADP-ribosyltransferase 1	ART1	Homo sapiens (human)	2	0	arthritis arthropathy astigmatism cancer central nervous system cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liver cancer mixed glioma nasopharynx carcinoma nephritis pancreatic cancer pancreatic carcinoma squamous cell carcinoma tongue squamous cell carcinoma tuberculosis
Q92643	GPI-anchor transamidase	PIGK GPI8	Homo sapiens (human)	3	1	adult lymphoma cancer central nervous system lymphoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer lymphoma obsolete ymphosarcoma
Q969N2	GPI transamidase component PIG-T	PIGT	Homo sapiens (human)	5	16	Marfan syndrome angioedema blindness brain disease breast cancer breast carcinoma calcinosis calcium metabolism disease cerebral degeneration congenital nystagmus craniosynostosis cystic kidney disease dermatographia diarrhea dissociated nystagmus epilepsy esotropia fibromyalgia hemolytic anemia hypercalcemia hyperopia hypertropia hypophosphatasia mechanical strabismus monocular esotropia multiple congenital anomalies-hypotonia-seizures syndrome 3 myositis nephrocalcinosis non-congenital cyst of kidney ophthalmoplegia osteoporosis paroxysmal nocturnal hemoglobinuria patent ductus arteriosus pathologic nystagmus phosphorus metabolism disease restrictive cardiomyopathy scoliosis situs inversus spontaneous ocular nystagmus strabismus tuberous sclerosis urticaria visual epilepsy
Q96S52	GPI transamidase component PIG-S	PIGS	Homo sapiens (human)	4	7	breast cancer cancer congenital nystagmus dissociated nystagmus embryoma epilepsy fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gingival hypertrophy gingival overgrowth hepatocellular carcinoma liver cancer microcephaly omphalocele pathologic nystagmus spontaneous ocular nystagmus umbilical hernia visual epilepsy
Q92521	GPI mannosyltransferase 3	PIGB	Homo sapiens (human)	2	0	axonal neuropathy epilepsy intellectual disability learning disability visual epilepsy
Q75T13	GPI inositol-deacylase	PGAP1	Homo sapiens (human)	4	6	Burkitt lymphoma Laron syndrome achondroplasia agnosia autosomal recessive intellectual developmental disorder brain disease cerebral degeneration choreatic disease congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy factor XII deficiency focal epilepsy fundus dystrophy holoprosencephaly 1 holoprosencephaly intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia paroxysmal nocturnal hemoglobinuria partial motor epilepsy stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
Q8TEQ8	GPI ethanolamine phosphate transferase 3	PIGO	Homo sapiens (human)	4	2	Cogan syndrome Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome absence epilepsy blepharospasm capillary disease childhood absence epilepsy cleft palate colorectal cancer colorectal carcinoma craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability monocular esotropia nonepidermolytic palmoplantar keratoderma oligohydramnios palmoplantar keratosis scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis visual epilepsy
Q5H8A4	GPI ethanolamine phosphate transferase 2	PIGG GPI7	Homo sapiens (human)	1	0	cerebral degeneration epilepsy intellectual disability learning disability placental insufficiency visual epilepsy
O95427	GPI ethanolamine phosphate transferase 1	PIGN MCD4	Homo sapiens (human)	4	8	Dandy-Walker syndrome Hirschsprung's disease Marfan syndrome Meckel syndrome Miller-Dieker lissencephaly syndrome Paget's disease of bone acute monocytic leukemia acute myeloid leukemia amblyopia 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 autosomal dominant polycystic kidney disease basal ganglia disease blepharitis blepharospasm cerebral degeneration chromosome 17p13.1 deletion syndrome chronic recurrent multifocal osteomyelitis cleft palate colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital nystagmus cryptorchidism dissociated nystagmus duodenal atresia epilepsy esophagitis esotropia essential thrombocythemia focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth heart septal defect holoprosencephaly 1 holoprosencephaly hydrocephalus hydronephrosis hypospadias idiopathic interstitial pneumonia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability lingual-facial-buccal dyskinesia lissencephaly lung adenocarcinoma lung cancer mammary Paget's disease microphthalmia monocular esotropia movement disease multiple congenital anomalies-hypotonia-seizures syndrome 1 myelodysplastic syndrome omphalocele patent ductus arteriosus patent foramen ovale pathologic nystagmus peptic esophagitis polyhydramnios postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary fibrosis recurrent corneal erosion renal agenesis situs inversus spontaneous ocular nystagmus strabismic amblyopia tetralogy of Fallot tuberous sclerosis umbilical hernia vesicoureteral reflux visual epilepsy
Q8IXQ4	GPALPP motifs-containing protein 1	GPALPP1 KIAA1704 LSR7	Homo sapiens (human)	4	2
Q3T8J9	GON-4-like protein	GON4L GON4 KIAA1606	Homo sapiens (human)	1	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements