GlyCosmos Portal

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UniProt ID	Protein Name ▼	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P34925	Tyrosine-protein kinase RYK	RYK JTK5A	5	0
Q12866	Tyrosine-protein kinase Mer	MERTK MER	18	28
P52333	Tyrosine-protein kinase JAK3	JAK3	1	1
O60674	Tyrosine-protein kinase JAK2	JAK2	0	1
P23458	Tyrosine-protein kinase JAK1	JAK1 JAK1A JAK1B	1	2
P08631	Tyrosine-protein kinase HCK	HCK	2	1
P06241	Tyrosine-protein kinase Fyn	FYN	0	1
P09769	Tyrosine-protein kinase Fgr	FGR SRC2	2	1
P16591	Tyrosine-protein kinase Fer	FER TYK3	0	1
P41240	Tyrosine-protein kinase CSK	CSK	0	1
Q06187	Tyrosine-protein kinase BTK	BTK AGMX1 ATK BPK	0	1
Q9UIG0	Tyrosine-protein kinase BAZ1B	BAZ1B WBSC10 WBSCR10 WBSCR9 WSTF	1	2
P42684	Tyrosine-protein kinase ABL2	ABL2 ABLL ARG	1	2
P00519	Tyrosine-protein kinase ABL1	ABL1 ABL JTK7	3	1
Q9Y2Z4	Tyrosine--tRNA ligase, mitochondrial	YARS2	1	1
P54577	Tyrosine--tRNA ligase, cytoplasmic	YARS1 YARS	3	1
P07101	Tyrosine 3-monooxygenase	TH TYH	0	1
P14679	Tyrosinase	TYR	7	0
P50052	Type-2 angiotensin II receptor	AGTR2	5	0
P30556	Type-1 angiotensin II receptor	AGTR1 AGTR1A AGTR1B AT2R1 AT2R1B	3	3
Q8IVY1	Type III endosome membrane protein TEMP	C1orf210	3	2
P32019	Type II inositol 1,4,5-trisphosphate 5-phosphatase	INPP5B OCRL2	0	1	Dent disease Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome amyotrophic lateral sclerosis 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 congenital hypothyroidism congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy giant cell glioblastoma glaucoma glioblastoma hypothyroidism limb-girdle muscular dystrophy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myxedema 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 progressive muscular atrophy rippling muscle disease 2
A0A0A8K8P7	Type I transmembrane receptor	PSK-1	2	0
Q9Y274	Type 2 lactosamine alpha-2,3-sialyltransferase	ST3GAL6 SIAT10	7	16	cancer carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer multiple myeloma sarcomatoid carcinoma stomach cancer
A0A087WXB8	Type 2 lactosamine alpha-2,3-sialyltransferase	ST3GAL6	1	0

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