GlyCosmos Portal

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The O-GlcNAc Database	June 3, 2024
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Displaying entries **110401 - 110425** 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
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
Q8NAU1	Fibronectin type III domain-containing protein 5	FNDC5 FRCP2	Homo sapiens (human)	2	0
Q8NAV1	Pre-mRNA-splicing factor 38A	PRPF38A	Homo sapiens (human)	0	1
Q8NAV2	Uncharacterized protein C8orf58	C8orf58	Homo sapiens (human)	0	1
Q8NB12	Histone-lysine N-methyltransferase SMYD1	SMYD1	Homo sapiens (human)	1	1
Q8NB14	Ubiquitin carboxyl-terminal hydrolase 38	USP38 KIAA1891	Homo sapiens (human)	0	1
Q8NB16	Mixed lineage kinase domain-like protein	MLKL	Homo sapiens (human)	4	1
Q8NB25	Protein FAM184A	FAM184A C6orf60	Homo sapiens (human)	0	1
Q8NB37	Glutamine amidotransferase-like class 1 domain-containing protein 1	GATD1 FERRY5 PDDC1	Homo sapiens (human)	1	0
Q8NB46	Serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C	ANKRD52	Homo sapiens (human)	0	1
Q8NB50	Zinc finger protein 62 homolog	ZFP62	Homo sapiens (human)	0	1
Q8NB66	Protein unc-13 homolog C	UNC13C	Homo sapiens (human)	0	1
Q8NB78	Lysine-specific histone demethylase 2	KDM1B AOF1 C6orf193 LSD2	Homo sapiens (human)	1	2
Q8NB90	ATPase family gene 2 protein homolog A	AFG2A SPAF SPATA5	Homo sapiens (human)	0	1
Q8NB91	Fanconi anemia group B protein	FANCB	Homo sapiens (human)	3	1
Q8NBA8	tRNA-uridine aminocarboxypropyltransferase 2	DTWD2	Homo sapiens (human)	1	1
Q8NBB4	Zinc finger and SCAN domain-containing protein 1	ZSCAN1	Homo sapiens (human)	0	1
Q8NBF2	NHL repeat-containing protein 2	NHLRC2	Homo sapiens (human)	1	1
Q8NBF6	Late secretory pathway protein AVL9 homolog	AVL9 KIAA0241	Homo sapiens (human)	3	1
Q8NBH2	Kyphoscoliosis peptidase	KY	Homo sapiens (human)	0	1
Q8NBI2	Lysosomal membrane ascorbate-dependent ferrireductase CYB561A3	CYB561A3 CYBASC3	Homo sapiens (human)	1	0
Q8NBI3	Draxin	DRAXIN C1orf187	Homo sapiens (human)	5	2
Q8NBI5	Equilibrative nucleobase transporter 1	SLC43A3 ENBT1	Homo sapiens (human)	4	4
Q8NBI6	Xyloside xylosyltransferase 1	XXYLT1 C3orf21	Homo sapiens (human)	4	2	atrial fibrillation bronchus cancer bronchus carcinoma cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma nicotine dependence obesity osteoporosis
Q8NBJ4	Golgi membrane protein 1	GOLM1 C9orf155 GOLPH2	Homo sapiens (human)	18	61

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