GlyCosmos Portal

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q00796	Sorbitol dehydrogenase	SORD	2	2	autosomal recessive distal hereditary motor neuronopathy 8
Q00839	Heterogeneous nuclear ribonucleoprotein U	C1orf199 HNRNPU HNRPU SAFA U21.1	8	3	developmental and epileptic encephalopathy 54
Q00872	Myosin-binding protein C, slow-type	MYBPC1 MYBPCS	1	0	congenital myopathy 16 distal arthrogryposis type 1B lethal congenital contracture syndrome 4
Q00887	Pregnancy-specific beta-1-glycoprotein 9	PSG11 PSG9	7	1
Q00888	Pregnancy-specific beta-1-glycoprotein 4	CGM4 PSG4 PSG9	7	1
Q00889	Pregnancy-specific beta-1-glycoprotein 6	CGM3 PSG10 PSG12 PSG6 PSGGB	7	0
Q00973	Beta-1,4 N-acetylgalactosaminyltransferase 1	B4GALNT1 GALGT SIAT2	3	0	hereditary spastic paraplegia 26
Q00975	Voltage-dependent N-type calcium channel subunit alpha-1B	CACH5 CACNA1B CACNL1A5	5	0	Lambert-Eaton myasthenic syndrome
Q00987	E3 ubiquitin-protein ligase Mdm2	MDM2	1	2	chronic myeloid leukemia glioblastoma hepatocellular carcinoma pancreatic ductal carcinoma sarcoma
Q00G26	Perilipin-5	LSDP5 OXPAT PAT-1 PLIN5	2	1
Q01082	Spectrin beta chain, non-erythrocytic 1	SPTB2 SPTBN1	33	3
Q01085	Nucleolysin TIAR	TIAL1	2	1
Q01094	Transcription factor E2F1	E2F1 RBBP3	3	1	lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma osteosarcoma pancreatic adenocarcinoma pancreatic ductal adenocarcinoma
Q01105	Protein SET	SET	2	2	autosomal dominant intellectual developmental disorder
Q01113	Interleukin-9 receptor	IL9R	2	0
Q01118	Sodium channel protein type 7 subunit alpha	SCN6A SCN7A	7	2
Q01130	Serine/arginine-rich splicing factor 2	SFRS2 SRSF2	1	1	acute myeloid leukemia congestive heart failure hepatocellular carcinoma myelodysplastic syndrome
Q01151	CD83 antigen	CD83	3	2
Q01167	Forkhead box protein K2	FOXK2 ILF ILF1	11	2
Q01196	Runt-related transcription factor 1	AML1 CBFA2 RUNX1	11	2	acute myeloid leukemia esophagus squamous cell carcinoma
Q01201	Transcription factor RelB	RELB	2	1	breast cancer immunodeficiency 53
Q01344	Interleukin-5 receptor subunit alpha	IL5R IL5RA	4	0	asthma
Q01433	AMP deaminase 2	AMPD2	2	1	hereditary spastic paraplegia 63 pontocerebellar hypoplasia type 9
Q01453	Peripheral myelin protein 22	GAS3 PMP22	1	0	Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease Guillain-Barre syndrome hereditary neuropathy with liability to pressure palsies
Q01459	Di-N-acetylchitobiase	CTB CTBS	4	19

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