GlyCosmos Portal

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P63096	Guanine nucleotide-binding protein G(i) subunit alpha-1	GNAI1	1	1
P63104	14-3-3 protein zeta/delta	YWHAZ	2	2
P63119	Endogenous retrovirus group K member 21 Pro protein	ERVK-21	3	1
P63135	Endogenous retrovirus group K member 7 Pol protein	ERVK-7	1	1
P63165	Small ubiquitin-related modifier 1	OK/SW-cl.43 SMT3C SMT3H3 SUMO1 UBL1	1	1	orofacial cleft 10
P63220	Small ribosomal subunit protein eS21	RPS21	1	1
P63241	Eukaryotic translation initiation factor 5A-1	EIF5A	1	1
P63244	Small ribosomal subunit protein RACK1	GNB2L1 HLC7 PIG21 RACK1	5	1
P63261	Actin, cytoplasmic 2	ACTG ACTG1	10	2	Baraitser-Winter syndrome 2 autosomal dominant nonsyndromic deafness 20
P63313	Thymosin beta-10	PTMB10 THYB10 TMSB10	3	1
P67809	Y-box-binding protein 1	NSEP1 YB1 YBX1	8	2
P67936	Tropomyosin alpha-4 chain	TPM4	1	1	blood platelet disease
P68032	Actin, alpha cardiac muscle 1	ACTC ACTC1	3	2	atrial heart septal defect 5 dilated cardiomyopathy 1R dilated cardiomyopathy hypertrophic cardiomyopathy 11
P68104	Elongation factor 1-alpha 1	EEF1A EEF1A1 EF1A LENG7	7	7
P68133	Actin, alpha skeletal muscle	ACTA ACTA1	4	1	congenital myopathy 2B congenital myopathy 2C nemaline myopathy 3
P68363	Tubulin alpha-1B chain	TUBA1B	21	2
P68366	Tubulin alpha-4A chain	TUBA1 TUBA4A	1	2	amyotrophic lateral sclerosis type 22
P68371	Tubulin beta-4B chain	TUBB2C TUBB4B	7	2	Leber congenital amaurosis with early-onset deafness
P68400	Casein kinase II subunit alpha	CK2A1 CSNK2A1	7	2
P68431	Histone H3.1	H3C1 H3C10 H3C11 H3C12 H3C2 H3C3 H3C4 H3C6 H3C7 H3C8 H3FA H3FB H3FC HIST1H3C H3FD H3FF H3FH H3FI H3FJ H3FK H3FL HIST1H3A HIST1H3B HIST1H3D HIST1H3E HIST1H3F HIST1H3G HIST1H3H HIST1H3I HIST1H3J	4	1
P68871	Hemoglobin subunit beta	HBB	10	2	Heinz body anemia acute chest syndrome alpha thalassemia autosomal dominant beta thalassemia beta thalassemia congenital hemolytic anemia delta beta-thalassemia familial erythrocytosis 6 hemoglobin C disease hemoglobinopathy malaria polycythemia sickle cell anemia sickle cell disease
P69849	BOS complex subunit NOMO3	NOMO3	7	11
P69905	Hemoglobin subunit alpha	HBA1 HBA2	10	1	Heinz body anemia alpha thalassemia familial erythrocytosis 7 hemoglobin H disease
P78310	Coxsackievirus and adenovirus receptor	CAR CXADR	10	22
P78312	Protein FAM193A	C4orf8 FAM193A RES4-22	17	3

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