GlyCosmos Portal

Displaying entries **15026 - 15050** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8TE96	ATP-dependent RNA helicase DQX1	DQX1	0	1
Q9BPU6	Dihydropyrimidinase-related protein 5	DPYSL5 CRMP5 ULIP6	0	1
O14531	Dihydropyrimidinase-related protein 4	DPYSL4 CRMP3 ULIP4	0	1
Q14195	Dihydropyrimidinase-related protein 3	DPYSL3 CRMP4 DRP3 ULIP ULIP1	0	1
Q16555	Dihydropyrimidinase-related protein 2	DPYSL2 CRMP2 ULIP2	11	5
Q12882	Dihydropyrimidine dehydrogenase [NADP(+)]	DPYD	4	1
Q9C005	Protein dpy-30 homolog	DPY30	0	1
Q7Z388	Probable C-mannosyltransferase DPY19L4	DPY19L4	3	10
Q6ZPD9	Protein C-mannosyl-transferase DPY19L3	DPY19L3	4	3	depressive disorder major depressive disorder melancholic depression obsolete melancholia
Q6ZN68	Putative C-mannosyltransferase DPY19L2P2	DPY19L2P2	1	0
Q2PZI1	Protein C-mannosyl-transferase DPY19L1	DPY19L1 GA0500 KIAA0877	0	1
Q07507	Dermatopontin	DPT	0	1
A6NFQ7	Divergent paired-related homeobox	DPRX	0	1
R4GMV4	Dipeptidyl peptidase 7	DPP7	1	0
Q9UHL4	Dipeptidyl peptidase 2	DPP7 DPP2 QPP	7	29
P42658	Dipeptidyl aminopeptidase-like protein 6	DPP6	8	6
A0A7I2V2R5	Dipeptidyl peptidase 4	DPP4	2	0
A0A7I2V2X8	Dipeptidyl peptidase 4	DPP4	2	0
A0A7I2V5R8	Dipeptidyl peptidase 4	DPP4	1	0
A0A7I2V2I2	dipeptidyl-peptidase IV	DPP4	1	0
F8WE17	dipeptidyl-peptidase IV	DPP4	1	0
P27487	Dipeptidyl peptidase 4	DPP4 ADCP2 CD26	12	84
Q9NY33	Dipeptidyl peptidase 3	DPP3	2	2
Q8N608	Inactive dipeptidyl peptidase 10	DPP10 DPRP3 KIAA1492	7	4
Q9P2X0	Dolichol-phosphate mannosyltransferase subunit 3	DPM3	2	2	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 cardiomyopathy clubfoot congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels 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

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