GlyCosmos Portal

Displaying entries **301 - 325** of **18496** in total

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9Y6J0	Calcineurin-binding protein cabin-1	CABIN1 KIAA0330	1	1
Q9Y6I9	Testis-expressed protein 264	TEX264 ZSIG11	2	3
Q9Y6I8	Peroxisomal membrane protein 4	PXMP4 PMP24	2	0
Q9Y6I3	Epsin-1	EPN1	4	2
Q9Y6H6	Potassium voltage-gated channel subfamily E member 3	KCNE3	3	0
Q9Y6H5	Synphilin-1	SNCAIP	1	1
Q9Y6H3	Mitochondrial inner membrane protease ATP23 homolog	ATP23 KUB3 XRCC6BP1	0	1
Q9Y6G9	Cytoplasmic dynein 1 light intermediate chain 1	DYNC1LI1 DNCLI1	8	1
Q9Y6G5	COMM domain-containing protein 10	COMMD10	0	1
Q9Y6G3	Large ribosomal subunit protein mL42	MRPL42 MRPL31 MRPS32 RPML31	0	1
Q9Y6F9	Protein Wnt-6	WNT6	2	0
Q9Y6E2	eIF5-mimic protein 1	BZW2 5MP1	2	1
Q9Y6E0	Serine/threonine-protein kinase 24	STK24 MST3 STK3	1	1
Q9Y6D9	Mitotic spindle assembly checkpoint protein MAD1	MAD1L1 MAD1 TXBP181	0	1
Q9Y6D6	Brefeldin A-inhibited guanine nucleotide-exchange protein 1	ARFGEF1 ARFGEP1 BIG1	1	3
Q9Y6D5	Brefeldin A-inhibited guanine nucleotide-exchange protein 2	ARFGEF2 ARFGEP2 BIG2	2	2
Q9Y6C9	Mitochondrial carrier homolog 2	MTCH2 MIMP	0	1
Q9Y6C5	Protein patched homolog 2	PTCH2	2	1
Q9Y6C2	EMILIN-1	EMILIN1 EMI	16	60
Q9Y6A9	Signal peptidase complex subunit 1	SPCS1 SPC12	0	1
Q9Y6A5	Transforming acidic coiled-coil-containing protein 3	TACC3 ERIC1	3	1
Q9Y6A4	Cilia- and flagella-associated protein 20	CFAP20 BUG22 C16orf80 GTL3	0	1
Q9Y6A2	Cholesterol 24-hydroxylase	CYP46A1 CYP46	2	1	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 Creutzfeldt-Jakob disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lennox-Gastaut syndrome Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 age related macular degeneration amyloidosis brain disease cancer cardiac arrest cerebral degeneration cerebrovascular disease chronic fatigue syndrome colorectal cancer colorectal carcinoma degeneration of macula and posterior pole depressive disorder diabetes mellitus dysthymic disorder encephalitis encephalomyelitis giant cell glioblastoma glioblastoma high grade glioma large intestine cancer macular degeneration major depressive disorder melancholic depression multiple sclerosis myelitis neurodegenerative disease neurotic disorder obsolete melancholia primary open angle glaucoma tauopathy type 2 diabetes mellitus
Q9Y6A1	Protein O-mannosyl-transferase 1	POMT1	5	8	Axenfeld-Rieger syndrome Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia blindness brain cancer brain disease buphthalmos campomelic dysplasia cardiomyopathy cataract centronuclear myopathy cleft lip cleft palate clubfoot coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy cornea plana cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus albipunctatus fundus dystrophy glaucoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hypertrophic cardiomyopathy hypertropia imperforate anus intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly locked-in syndrome mechanical strabismus megaconial type congenital muscular dystrophy megalocornea meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia myositis nemaline myopathy neuromuscular disease obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy oligohydramnios ophthalmoplegia optic atrophy peripheral retinal degeneration placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 quadriplegia recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rigid spine muscular dystrophy 1 rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type tuberous sclerosis visual epilepsy
Q9Y698	Voltage-dependent calcium channel gamma-2 subunit	CACNG2	1	1

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