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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8NBP5	Major facilitator superfamily domain-containing protein 9	MFSD9	1	1
Q8NBN7	Retinol dehydrogenase 13	RDH13 SDR7C3	0	1
Q8NBN3	Transmembrane protein 87A	TMEM87A	6	41
Q8NBM8	Prenylcysteine oxidase-like	PCYOX1L	1	0
Q8NBM4	Ubiquitin-associated domain-containing protein 2	UBAC2 PHGDHL1	1	1
Q8NBL3	Transmembrane protein 178A	TMEM178A TMEM178	1	0
Q8NBL1	Protein O-glucosyltransferase 1	POGLUT1 C3orf9 CLP46 KTELC1 MDSRP	5	23	Dowling-Degos disease Duchenne muscular dystrophy T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia 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 cancer childhood T-cell acute lymphoblastic leukemia childhood leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital muscular dystrophy distal myopathy embryoma essential thrombocythemia facioscapulohumeral muscular dystrophy hematopoietic system disease isolated elevated serum creatine phosphokinase levels keratosis follicularis large intestine cancer leukemia limb-girdle muscular dystrophy lung cancer lung non-small cell carcinoma mongolian spot muscular dystrophy myelodysplastic syndrome 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 oculopharyngeal muscular dystrophy primary biliary cholangitis pseudoxanthoma elasticum reticulate acropigmentation of Kitamura rippling muscle disease 2
Q8NBK3	Formylglycine-generating enzyme	SUMF1	2	12	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
Q8NBJ9	SID1 transmembrane family member 2	SIDT2	11	8
Q8NBJ7	Inactive C-alpha-formylglycine-generating enzyme 2	SUMF2	6	21
Q8NBJ5	Procollagen galactosyltransferase 1	COLGALT1 GLT25D1	5	31	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
Q8NBJ4	Golgi membrane protein 1	GOLM1 C9orf155 GOLPH2	18	61
Q8NBI6	Xyloside xylosyltransferase 1	XXYLT1 C3orf21	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
Q8NBI5	Equilibrative nucleobase transporter 1	SLC43A3 ENBT1	4	4
Q8NBI3	Draxin	DRAXIN C1orf187	5	2
Q8NBI2	Lysosomal membrane ascorbate-dependent ferrireductase CYB561A3	CYB561A3 CYBASC3	1	0
Q8NBH2	Kyphoscoliosis peptidase	KY	0	1
Q8NBF6	Late secretory pathway protein AVL9 homolog	AVL9 KIAA0241	3	1
Q8NBF2	NHL repeat-containing protein 2	NHLRC2	1	1
Q8NBB4	Zinc finger and SCAN domain-containing protein 1	ZSCAN1	0	1
Q8NBA8	tRNA-uridine aminocarboxypropyltransferase 2	DTWD2	1	1
Q8NB91	Fanconi anemia group B protein	FANCB	3	1
Q8NB90	ATPase family gene 2 protein homolog A	AFG2A SPAF SPATA5	0	1
Q8NB78	Lysine-specific histone demethylase 2	KDM1B AOF1 C6orf193 LSD2	1	2
Q8NB66	Protein unc-13 homolog C	UNC13C	0	1

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