GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **4126 - 4150** 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
E9PZD0	Signal-regulatory protein beta 1C	Sirpb1c	Mus musculus (house mouse)	1	0
V5DLG6	U-box domain protein	TCDM_03040	Trypanosoma cruzi Dm28c	0	1
A0A6J5UCJ9	Xyloglucan endotransglucosylase/hydrolase	CURHAP_LOCUS22142	Prunus armeniaca (apricot)	1	0
A0A669Q5K7	Angiotensin-converting enzyme	ACE2	Phasianus colchicus (Ring-necked pheasant)	1	0
F6W3Q8	Procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 (Fragment)	Plod3	Mus musculus (house mouse)	1	0
E9Q6A3	Sorbin and SH3 domain containing 1	Sorbs1	Mus musculus (house mouse)	2	1
Q92508	Piezo-type mechanosensitive ion channel component 1	PIEZO1 FAM38A KIAA0233	Homo sapiens (human)	3	10
A0A851SBB8	Hyaluronidase (Fragment)	Hyal	Certhia familiaris (Eurasian tree-creeper)	1	0
Q9ERZ4	Muscarinic acetylcholine receptor M2	Chrm2 Chrm-2	Mus musculus (house mouse)	3	0
B2YG98	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q8NAT1	Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2	POMGNT2 AGO61 C3orf39 EOGTL GTDC2	Homo sapiens (human)	6	8	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome acute myeloid leukemia 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 cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly malaria microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
A0A7K6LF24	Fibroblast growth factor receptor 2 (Fragment)	Fgfr2	Falcunculus frontatus (Eastern shriketit)	8	0
Q6VF02	Rhodopsin (Fragment)	Rhod	Boophis luteus	1	0
P59684	Tumor necrosis factor	TNF TNFA TNFSF2	Bos indicus (zebu cattle)	1	0
O95297	Myelin protein zero-like protein 1	MPZL1 PZR	Homo sapiens (human)	5	55
P0C0S8	Histone H2A type 1	H2AC11 H2AC13 H2AC15 H2AC16 H2AC17 H2AFC H2AFD H2AFI H2AFN H2AFP HIST1H2AG HIST1H2AI HIST1H2AK HIST1H2AL HIST1H2AM	Homo sapiens (human)	1	1
B6KDN4	Kinesin heavy chain, putative	BN1205_020810	Toxoplasma gondii VEG	0	1
Q07DX7	Protein Wnt-2	WNT2	Nomascus leucogenys (northern white-cheeked gibbon)	1	0
Q59288	Chondroitinase-AC	cslA chnAC	Pedobacter heparinus DSM 2366	2	0
A0A674NE63	Proto-oncogene tyrosine-protein kinase receptor Ret	ret	Takifugu rubripes (torafugu)	1	0
Q9M1E7	Tetraspanin-3	TET3	Arabidopsis thaliana (thale cress)	2	0
A0A852GJJ3	Angiotensin-converting enzyme (Fragment)	Ace	Larus smithsonianus (American herring gull)	3	0
A0A7J0E1Z3	Xyloglucan endotransglucosylase/hydrolase	Acr_01g0003320	Actinidia rufa	1	0
Q95121	Pigment epithelium-derived factor	SERPINF1 PEDF	Bos taurus (cattle)	1	0
A0A4D5ZBE7	Pre-glycoprotein polyprotein GP complex	GPC	Mammarenavirus lassaense	11	0

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