GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9H0U3	Magnesium transporter protein 1	MAGT1 IAG2	1	2
Q13029	PR domain zinc finger protein 2	PRDM2 KMT8 RIZ	3	2
O60883	G-protein coupled receptor 37-like 1	GPR37L1 ETBRLP2	7	2
P30153	Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform	PPP2R1A	2	2
Q8TEJ3	E3 ubiquitin-protein ligase SH3RF3	SH3RF3 POSH2 SH3MD4	3	2
P51531	Probable global transcription activator SNF2L2	SMARCA2 BAF190B BRM SNF2A SNF2L2	7	2
Q12849	G-rich sequence factor 1	GRSF1	4	2
Q8IZP0	Abl interactor 1	ABI1 SSH3BP1	1	2
Q9UJU2	Lymphoid enhancer-binding factor 1	LEF1	1	2
Q9BSJ8	Extended synaptotagmin-1	ESYT1 FAM62A KIAA0747 MBC2	2	2
Q14573	Inositol 1,4,5-trisphosphate receptor type 3	ITPR3	4	2
O43189	PHD finger protein 1	PHF1 PCL1	1	2
Q9Y2X9	Zinc finger protein 281	ZNF281 GZP1 ZBP99	30	2
P61758	Prefoldin subunit 3	VBP1 PFDN3	1	2
O00231	26S proteasome non-ATPase regulatory subunit 11	PSMD11	1	2
Q9NSC7	Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	ST6GALNAC1 SIAT7A	11	2	acute myocardial infarction bladder carcinoma breast cancer cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary thrombosis embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer myocardial infarction ovarian cancer ovarian carcinoma schizophrenia silent myocardial infarction stomach cancer stomach carcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer
P63261	Actin, cytoplasmic 2	ACTG1 ACTG	10	2
Q15075	Early endosome antigen 1	EEA1 ZFYVE2	4	2
Q9Y2B1	Ribitol-5-phosphate xylosyltransferase 1	RXYLT1 TMEM5	4	2	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Turner syndrome Walker-Warburg syndrome 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 disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A10 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma gonadal dysgenesis hydranencephaly hydrocephalus intellectual disability learning disability limb-girdle muscular dystrophy lissencephaly 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
Q16204	Coiled-coil domain-containing protein 6	CCDC6 D10S170 TST1	5	2
Q9BPX7	UPF0415 protein C7orf25	C7orf25	1	2
O15409	Forkhead box protein P2	FOXP2 CAGH44 TNRC10	2	2
O60610	Protein diaphanous homolog 1	DIAPH1 DIAP1	6	2
P55010	Eukaryotic translation initiation factor 5	EIF5	2	2
Q04941	Proteolipid protein 2	PLP2 A4	5	2

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