GlyCosmos Portal

Displaying entries **14626 - 14650** of **18496** in total

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q92956	Tumor necrosis factor receptor superfamily member 14	TNFRSF14 HVEA HVEM	3	1
Q92959	Solute carrier organic anion transporter family member 2A1	SLCO2A1 OATP2A1 SLC21A2	3	0
Q92973	Transportin-1	TNPO1 KPNB2 MIP1 TRN	1	1
Q92974	Rho guanine nucleotide exchange factor 2	ARHGEF2 KIAA0651 LFP40	1	1
Q92979	Ribosomal RNA small subunit methyltransferase NEP1	EMG1 C2F	0	1
Q92982	Ninjurin-1	NINJ1	1	0
Q92985	Interferon regulatory factor 7	IRF7	1	1
Q92990	Glomulin	GLMN FAP48 FAP68 VMGLOM	2	1
Q92993	Histone acetyltransferase KAT5	KAT5 HTATIP TIP60	0	1
Q92994	Transcription factor IIIB 90 kDa subunit	BRF1 BRF GTF3B TAF3B2 TAF3C	0	1
Q92995	Ubiquitin carboxyl-terminal hydrolase 13	USP13 ISOT3	0	1
Q92997	Segment polarity protein dishevelled homolog DVL-3	DVL3 KIAA0208	6	1
Q93008	Ubiquitin carboxyl-terminal hydrolase 9X	USP9X DFFRX FAM USP9	0	1
Q93009	Ubiquitin carboxyl-terminal hydrolase 7	USP7 HAUSP	3	2
Q93033	Immunoglobulin superfamily member 2	CD101 EWI101 IGSF2 V7	4	2
Q93034	Cullin-5	CUL5 VACM1	1	2
Q93038	Tumor necrosis factor receptor superfamily member 25	TNFRSF25 APO3 DDR3 DR3 TNFRSF12 WSL WSL1	8	1
Q93045	Stathmin-2	STMN2 SCG10 SCGN10	0	1
Q93050	V-type proton ATPase 116 kDa subunit a 1	ATP6V0A1 ATP6N1 ATP6N1A VPP1	1	4
Q93052	Lipoma-preferred partner	LPP	15	5
Q93062	RNA-binding protein with multiple splicing	RBPMS HERMES	0	1
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
Q93070	Ecto-ADP-ribosyltransferase 4	ART4 DO DOK1	5	23	carotid artery thrombosis carotid stenosis conjunctivitis
Q93073	Selenocysteine insertion sequence-binding protein 2-like	SECISBP2L KIAA0256	1	1
Q93074	Mediator of RNA polymerase II transcription subunit 12	MED12 ARC240 CAGH45 HOPA KIAA0192 TNRC11 TRAP230	0	1

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