GlyCosmos Portal

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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 **5101 - 5125** of **126547** in total

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UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9Y6A1	Protein O-mannosyl-transferase 1	POMT1	Homo sapiens (human)	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	Homo sapiens (human)	1	1
Q9Y697	Cysteine desulfurase	NFS1 NIFS	Homo sapiens (human)	0	1
Q9Y696	Chloride intracellular channel protein 4	CLIC4	Homo sapiens (human)	0	1
Q9Y694	Solute carrier family 22 member 7	SLC22A7 NLT OAT2	Homo sapiens (human)	2	2
Q9Y692	Glucocorticoid modulatory element-binding protein 1	GMEB1	Homo sapiens (human)	13	2
Q9Y691	Calcium-activated potassium channel subunit beta-2	KCNMB2	Homo sapiens (human)	3	0
Q9Y680	Peptidyl-prolyl cis-trans isomerase FKBP7	FKBP7 FKBP23	Homo sapiens (human)	1	8
Q9Y678	Coatomer subunit gamma-1	COPG1 COPG	Homo sapiens (human)	18	1
Q9Y676	Small ribosomal subunit protein mS40	MRPS18B C6orf14	Homo sapiens (human)	0	1
Q9Y673	Dolichyl-phosphate beta-glucosyltransferase	ALG5	Homo sapiens (human)	1	1
Q9Y672	Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase	ALG6	Homo sapiens (human)	1	0	antithrombin III deficiency congenital disorder of glycosylation Ia congenital disorder of glycosylation Ic congenital disorder of glycosylation type I congenital disorder of glycosylation epilepsy hypertropia mechanical strabismus ophthalmoplegia protein C deficiency protein S deficiency strabismus thrombophilia visual epilepsy
Q9Y666	Solute carrier family 12 member 7	SLC12A7 KCC4	Homo sapiens (human)	3	7
Q9Y663	Heparan sulfate glucosamine 3-O-sulfotransferase 3A1	HS3ST3A1 3OST3A1 HS3ST3A	Homo sapiens (human)	2	0	breast cancer breast carcinoma
Q9Y662	Heparan sulfate glucosamine 3-O-sulfotransferase 3B1	HS3ST3B1 3OST3B1 HS3ST3B	Homo sapiens (human)	5	1	bladder carcinoma breast cancer endometriosis of ovary endometriosis of uterus endometriosis hepatitis B lung cancer lung non-small cell carcinoma pancreatic cancer pancreatic carcinoma urinary bladder cancer
Q9Y661	Heparan sulfate glucosamine 3-O-sulfotransferase 4	HS3ST4 3OST4	Homo sapiens (human)	4	0	acute lymphoblastic leukemia age related macular degeneration amphetamine abuse degeneration of macula and posterior pole lymphoblastic lymphoma macular degeneration
Q9Y657	Spindlin-1	SPIN1 OCR SPIN	Homo sapiens (human)	0	1
Q9Y653	Adhesion G-protein coupled receptor G1	ADGRG1 GPR56 TM7LN4 TM7XN1	Homo sapiens (human)	10	30
Q9Y646	Carboxypeptidase Q	CPQ LCH1 PGCP	Homo sapiens (human)	5	83
Q9Y644	Beta-1,3-N-acetylglucosaminyltransferase radical fringe	RFNG	Homo sapiens (human)	2	2
Q9Y639	Neuroplastin	NPTN SDFR1 SDR1	Homo sapiens (human)	8	37
Q9Y625	Glypican-6	GPC6	Homo sapiens (human)	3	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 Pick's disease Reye syndrome Simpson-Golabi-Behmel syndrome type 1 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 blepharophimosis breast cancer breast carcinoma cancer cardiovascular system disease cavernous hemangioma cerebral degeneration chorioangioma colorectal cancer colorectal carcinoma craniosynostosis cryptorchidism degenerative disc disease dissociative disorder embryoma enterocele familial retinoblastoma glomus tumor heart disease hemangioma histiocytoid hemangioma intellectual disability intramuscular hemangioma large intestine cancer learning disability lymphangioma melanoma neurotic disorder omodysplasia omphalocele osteoporosis ovarian cancer ovarian carcinoma patent foramen ovale pterygium reflex sympathetic dystrophy retinoblastoma schizophrenia skin melanoma trilateral retinoblastoma umbilical hernia ventricular septal defect
Q9Y624	Junctional adhesion molecule A	F11R JAM1 JCAM	Homo sapiens (human)	4	16
Q9Y623	Myosin-4	MYH4	Homo sapiens (human)	0	1
Q9Y620	DNA repair and recombination protein RAD54B	RAD54B	Homo sapiens (human)	0	1

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