GlyCosmos Portal

Displaying entries **4901 - 4925** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
P40198	Carcinoembryonic antigen-related cell adhesion molecule 3	CEACAM3 CD66D CGM1	2	0
Q5JWQ4	Neuropilin 1	NRP1	2	0
A0A7I2YQ92	Cathepsin H	CTSH	2	0
Q9BZF9	Uveal autoantigen with coiled-coil domains and ankyrin repeats	UACA KIAA1561	2	2
O43292	Glycosylphosphatidylinositol anchor attachment 1 protein	GPAA1 GAA1	2	0	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Cogan syndrome Friedreich ataxia 1 Friedreich ataxia Pick's disease Reye syndrome agnosia apraxia bladder carcinoma blindness breast cancer breast carcinoma cancer cerebral degeneration colorectal cancer colorectal carcinoma congenital nystagmus diffuse interstitial keratitis dissociated nystagmus embryoma epilepsy head and neck squamous cell carcinoma hepatocellular carcinoma intellectual disability large intestine cancer learning disability liver cancer liver cirrhosis myopia optic atrophy osteoporosis pathologic nystagmus spontaneous ocular nystagmus squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma tongue squamous cell carcinoma urinary bladder cancer visual epilepsy
Q15403	Pregnancy-specific protein (Fragment)	SP1	2	0
Q9BPZ7	Target of rapamycin complex 2 subunit MAPKAP1	MAPKAP1 MIP1 SIN1	2	1
Q8NHX9	Two pore channel protein 2	TPCN2 TPC2	2	0
Q93097	Protein Wnt-2b	WNT2B WNT13	2	0
P63010	AP-2 complex subunit beta	AP2B1 ADTB2 CLAPB1	2	1
P54296	Myomesin-2	MYOM2	2	1
Q9Y6D5	Brefeldin A-inhibited guanine nucleotide-exchange protein 2	ARFGEF2 ARFGEP2 BIG2	2	2
Q9ULD6	Protein inturned	INTU KIAA1284 PDZD6 PDZK6	2	1
P48546	Gastric inhibitory polypeptide receptor	GIPR	2	0
P0C7P4	Putative cytochrome b-c1 complex subunit Rieske-like protein 1	UQCRFS1P1 UQCRFSL1	2	1
Q9NR23	Growth/differentiation factor 3	GDF3	2	0
Q05086	Ubiquitin-protein ligase E3A	UBE3A E6AP EPVE6AP HPVE6A	2	2
O60927	E3 ubiquitin-protein ligase PPP1R11	PPP1R11 HCGV TCTE5	2	1
P35410	Mas-related G-protein coupled receptor MRG	MAS1L MRG	2	0
H0YA68	Alpha-mannosidase (Fragment)	MAN2B2	2	0
Q9H7U1	Serine-rich coiled-coil domain-containing protein 2	CCSER2 FAM190B KIAA1128	2	1
E9PP43	Sortilin related receptor 1	SORL1	2	0
Q93063	Exostosin-2	EXT2	2	2	Alzheimer's disease Cenani-Lenz syndactyly syndrome Dent disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Marfan syndrome Ollier disease Pick's disease Reye syndrome achondroplasia adenosarcoma agnosia anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease cerebral degeneration cherubism chondrosarcoma cleidocranial dysplasia clubfoot congenital hypothyroidism congenital nystagmus connective tissue disease cranial nerve disease cranial nerve palsy craniosynostosis cryptorchidism developmental and epileptic encephalopathy 36 developmental coordination disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus epilepsy esophagitis essential hypertension exostosis familial hypercholesterolemia frontotemporal dementia gastroesophageal reflux disease hereditary multiple exostoses humeroradial synostosis hyperostosis hypertension hypertropia hypothyroidism immune system disease intellectual disability large intestine cancer learning disability lupus nephritis macrocytic anemia mechanical strabismus membranous glomerulonephritis metachondromatosis microcephaly mucopolysaccharidosis III mucopolysaccharidosis type IIIA myxedema nephroblastoma nonsyndromic congenital nail disorder 9 obsolete constipation ophthalmoplegia osteoarthritis osteonecrosis osteosarcoma parietal foramina pathologic nystagmus peptic esophagitis periarthritis radioulnar synostosis scoliosis situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus tendinitis tuberous sclerosis type 2 diabetes mellitus ventricular septal defect visual epilepsy
Q99680	G-protein coupled receptor 22	GPR22	2	0
Q9NRH2	SNF-related serine/threonine-protein kinase	SNRK KIAA0096 SNFRK	2	1

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