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UniProt ID	Protein Name	Gene Symbol	No. of GlyTouCan IDs	Disease Ontology
Q969Y2	tRNA modification GTPase GTPBP3, mitochondrial	GTPBP3 MTGP1	1
Q9NS56	E3 ubiquitin-protein ligase Topors	TOPORS LUN TP53BPL	1
Q6PFW1	Inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1	PPIP5K1 HISPPD2A IP6K IPS1 KIAA0377 VIP1	1
A1A5D9	BICD family-like cargo adapter 2	BICDL2 BICDR2 CCDC64B	1
P48741	Putative heat shock 70 kDa protein 7	HSPA7 HSP70B	1
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

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