GlyCosmos Portal

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8NA70	Protein FAM47B	FAM47B	0	1
Q8NA72	Centrosomal protein POC5	POC5 C5orf37	1	2
Q8NA82	Probable E3 ubiquitin-protein ligase MARCHF10	MARCHF10 MARCH10 RNF190	3	1
Q8NAA5	Leucine-rich repeat-containing protein 75A	LRRC75A C17orf76 FAM211A	1	1
Q8NAA6	Putative uncharacterized protein encoded by LINC02694	LINC02694 C15orf53	0	1
Q8NAB2	Kelch repeat and BTB domain-containing protein 3	KBTBD3 BKLHD3	0	1
Q8NAC3	Interleukin-17 receptor C	IL17RC	9	0
Q8NAJ2	Putative uncharacterized protein encoded by LINC02913	LINC02913 C9orf106	0	1
Q8NAP1	Putative protein CASTOR3P	CASTOR3P CASTOR3 GATS STAG3OS	1	1
Q8NAP3	Zinc finger and BTB domain-containing protein 38	ZBTB38	1	1
Q8NAT1	Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2	POMGNT2 AGO61 C3orf39 EOGTL GTDC2	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
Q8NAU1	Fibronectin type III domain-containing protein 5	FNDC5 FRCP2	2	0
Q8NAV1	Pre-mRNA-splicing factor 38A	PRPF38A	0	1
Q8NAV2	Uncharacterized protein C8orf58	C8orf58	0	1
Q8NB12	Histone-lysine N-methyltransferase SMYD1	SMYD1	1	1
Q8NB14	Ubiquitin carboxyl-terminal hydrolase 38	USP38 KIAA1891	0	1
Q8NB16	Mixed lineage kinase domain-like protein	MLKL	4	1
Q8NB25	Protein FAM184A	FAM184A C6orf60	0	1
Q8NB37	Glutamine amidotransferase-like class 1 domain-containing protein 1	GATD1 FERRY5 PDDC1	1	0
Q8NB46	Serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C	ANKRD52	0	1
Q8NB50	Zinc finger protein 62 homolog	ZFP62	0	1
Q8NB66	Protein unc-13 homolog C	UNC13C	0	1
Q8NB78	Lysine-specific histone demethylase 2	KDM1B AOF1 C6orf193 LSD2	1	2
Q8NB90	ATPase family gene 2 protein homolog A	AFG2A SPAF SPATA5	0	1
Q8NB91	Fanconi anemia group B protein	FANCB	3	1

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