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UniProt ID	Protein Name	Gene Symbol	No. of GlyTouCan IDs	Disease Ontology
O95807	Transmembrane protein 50A	TMEM50A SMP1	1
Q96BD6	SPRY domain-containing SOCS box protein 1	SPSB1 SSB1	1
A6PVC2	Protein monoglycylase TTLL8	TTLL8	1
P22090	Small ribosomal subunit protein eS4, Y isoform 1	RPS4Y1 RPS4Y	1
O94768	Serine/threonine-protein kinase 17B	STK17B DRAK2	1
Q58FG0	Putative heat shock protein HSP 90-alpha A5	HSP90AA5P HSP90AE	1
Q96P20	NACHT, LRR and PYD domains-containing protein 3	NLRP3 C1orf7 CIAS1 NALP3 PYPAF1	1
P23490	Loricrin	LORICRIN LOR LRN	1
Q9NPJ1	Molecular chaperone MKKS	MKKS BBS6	1
Q9UKD2	mRNA turnover protein 4 homolog	MRTO4 C1orf33 MRT4	1
P49458	Signal recognition particle 9 kDa protein	SRP9	1
Q9UBT3	Dickkopf-related protein 4	DKK4	1
Q9Y2I6	Ninein-like protein	NINL KIAA0980 NLP	1
Q9BXG8	Spermatogenic leucine zipper protein 1	SPZ1 TSP1	1
Q8NHP6	Motile sperm domain-containing protein 2	MOSPD2	1
P48729	Casein kinase I isoform alpha	CSNK1A1	1
Q8NHY0	Beta-1,4 N-acetylgalactosaminyltransferase 2	B4GALNT2 GALGT2	1	Duchenne muscular dystrophy 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 campomelic dysplasia cancer carcinoma cerebrotendinous xanthomatosis congenital muscular dystrophy coronary artery disease distal myopathy embryoma facioscapulohumeral muscular dystrophy limb-girdle muscular dystrophy 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 oculopharyngeal muscular dystrophy rippling muscle disease 2 sarcomatoid carcinoma
P53611	Geranylgeranyl transferase type-2 subunit beta	RABGGTB GGTB	1
Q16891	MICOS complex subunit MIC60	IMMT HMP MIC60 MINOS2	1
Q9NVK5	FGFR1 oncogene partner 2	FGFR1OP2	1
Q8N335	Glycerol-3-phosphate dehydrogenase 1-like protein	GPD1L KIAA0089	1	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation congestive heart failure coronary artery disease head and neck squamous cell carcinoma nutmeg liver osteoarthritis sick sinus syndrome steatotic liver disease sudden infant death syndrome
P43897	Elongation factor Ts, mitochondrial	TSFM	1
Q96NL6	Sodium channel and clathrin linker 1	SCLT1 SAP1	1
O75525	KH domain-containing, RNA-binding, signal transduction-associated protein 3	KHDRBS3 SALP SLM2	1
P56962	Syntaxin-17	STX17	1

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