GlyCosmos Portal

Displaying entries **2101 - 2125** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
O94901	SUN domain-containing protein 1	SUN1 KIAA0810 UNC84A	5	15
Q6P4Q7	Metal transporter CNNM4	CNNM4 ACDP4 KIAA1592	5	13
Q7Z3X3	N-acetylglucosamine-6-sulfatase	DKFZp686E12166	5	0
Q13263	Transcription intermediary factor 1-beta	TRIM28 KAP1 RNF96 TIF1B	5	2
Q9BXX3	Ankyrin repeat domain-containing protein 30A	ANKRD30A	5	1
O75044	SLIT-ROBO Rho GTPase-activating protein 2	SRGAP2 ARHGAP34 FNBP2 KIAA0456 SRGAP2A	5	1
Q496J9	Synaptic vesicle glycoprotein 2C	SV2C KIAA1054	5	1
Q13698	Voltage-dependent L-type calcium channel subunit alpha-1S	CACNA1S CACH1 CACN1 CACNL1A3	5	1
Q2MV58	Tectonic-1	TCTN1 TECT1	5	4
Q9Y6R4	Mitogen-activated protein kinase kinase kinase 4	MAP3K4 KIAA0213 MAPKKK4 MEKK4 MTK1	5	1
Q8N183	NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2	NDUFAF2 NDUFA12L	5	1
P38606	V-type proton ATPase catalytic subunit A	ATP6V1A ATP6A1 ATP6V1A1 VPP2	5	1	American histoplasmosis Dandy-Walker syndrome Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Unverricht-Lundborg syndrome achondroplasia agnosia angioma serpiginosum anodontia aspergillosis 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 attention deficit hyperactivity disorder autistic disorder autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID black piedra blepharophimosis blepharospasm brain disease capillary hemangioma cardiomyopathy cataract cavernous hemangioma cerebral degeneration clubfoot coccidioidomycosis coloboma colorectal cancer colorectal carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital nystagmus congenital ptosis congestive heart failure cortical dysplasia-focal epilepsy syndrome cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder dissociated nystagmus dystonia early myoclonic encephalopathy endomyocardial fibrosis entropion epilepsy esophagitis familial hypertrophic cardiomyopathy focal hand dystonia gastroesophageal reflux disease histoplasmosis hydranencephaly hyperopia hypertrophic cardiomyopathy hypertropia inguinal hernia intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia lipoatrophic diabetes mellitus lipodystrophy lissencephaly mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy ophthalmoplegia optic atrophy patent foramen ovale pathologic nystagmus peptic esophagitis placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 ptosis retinal degeneration schizophrenia septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly spontaneous ocular nystagmus sporotrichosis status epilepticus stomach cancer stomach carcinoma strabismus superficial mycosis syndromic X-linked intellectual disability Najm type tooth agenesis visual epilepsy white piedra
Q9H7M9	V-type immunoglobulin domain-containing suppressor of T-cell activation	VSIR C10orf54 SISP1 VISTA	5	15
Q9C0B0	RING finger protein unkempt homolog	UNK KIAA1753 ZC3H5 ZC3HDC5	5	2
Q15032	R3H domain-containing protein 1	R3HDM1 KIAA0029 R3HDM	5	2
O95388	CCN family member 4	CCN4 WISP1	5	1
P48029	Sodium- and chloride-dependent creatine transporter 1	SLC6A8	5	3
Q8NCW0	Kremen protein 2	KREMEN2 KRM2	5	1
Q92478	C-type lectin domain family 2 member B	CLEC2B AICL CLECSF2 IFNRG1	5	1	cancer hepatocellular carcinoma liver cancer
Q9UMR5	Lysosomal thioesterase PPT2	PPT2	5	8	cancer cerebellar ataxia cerebellar disease embryoma histiocytosis membranous glomerulonephritis multiple myeloma multiple sclerosis neuroblastoma neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis
Q8TDB8	Solute carrier family 2, facilitated glucose transporter member 14	SLC2A14 GLUT14	5	2
Q92878	DNA repair protein RAD50	RAD50	5	1
Q16832	Discoidin domain-containing receptor 2	DDR2 NTRKR3 TKT TYRO10	5	0
Q0JRZ9	F-BAR domain only protein 2	FCHO2	5	1
Q9H4F1	Alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase	ST6GALNAC4 SIAT3C SIAT7D	5	3	Guillain-Barre syndrome Miller Fisher syndrome cancer thyroid gland follicular carcinoma

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