GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
Q6NUQ1	RAD50-interacting protein 1	RINT1	2	1
Q96RQ3	Methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial	MCCC1 MCCA	2	2
A0A3B3IRN5	Fibromodulin	FMOD	2	0
Q7Z7K9	LDL receptor related protein 1	LRP1	2	0
Q13613	Myotubularin-related protein 1	MTMR1	2	2	Charcot-Marie-Tooth disease type 4B1 centronuclear myopathy X-linked centronuclear myopathy congenital structural myopathy myotonic dystrophy type 1 myotonic dystrophy type 2
Q8NGG0	Olfactory receptor 8J3	OR8J3	2	0
A0A7I2YQH8	Cathepsin F	CTSF	2	0
Q6N075	Molybdate-anion transporter	MFSD5	2	1
Q8N349	Olfactory receptor 2L13	OR2L13 OR2L14	2	0
Q9UN71	Protocadherin gamma-B4	PCDHGB4 CDH20 FIB2	2	4
Q9UBJ2	ATP-binding cassette sub-family D member 2	ABCD2 ALD1 ALDL1 ALDR ALDRP	2	0
A0JNW5	Bridge-like lipid transfer protein family member 3B	BLTP3B KIAA0701 SHIP164 UHRF1BP1L	2	3
Q9NRL3	Striatin-4	STRN4 ZIN	2	1
E9PQY3	Lysosomal acid phosphatase	ACP2	2	0
Q9H3H5	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	DPAGT1 DPAGT2	2	2	Bell's palsy Ebola hemorrhagic fever Lambert-Eaton myasthenic syndrome acute intermittent porphyria agnosia alternating exotropia breast cancer cancer cataract clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ij congenital disorder of glycosylation type I congenital disorder of glycosylation congenital myasthenic syndrome 13 congenital myasthenic syndrome congenital nystagmus congenital ptosis cutaneous leishmaniasis developmental and epileptic encephalopathy 36 developmental coordination disorder dissociated nystagmus epilepsy essential hypertension exotropia facial nerve disease facial paralysis familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome glycoproteinosis hepatocellular carcinoma hypertension intellectual disability isolated elevated serum creatine phosphokinase levels large intestine cancer learning disability leishmaniasis liver cancer microcephaly monocular exotropia mucolipidosis II alpha/beta myopathy pathologic nystagmus pseudosarcomatous fibromatosis ptosis scoliosis spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma stuttering syndromic X-linked intellectual disability 94 tongue squamous cell carcinoma tuberculosis visceral leishmaniasis visual epilepsy
Q4FZB7	Histone-lysine N-methyltransferase KMT5B	KMT5B SUV420H1	2	5
P10323	Acrosin	ACR ACRS	2	1
A0A7I2V3T9	Pro-cathepsin H	CTSH	2	0
A0A7I2V3M3	Cathepsin F	CTSF	2	0
Q9C0K7	STE20-related kinase adapter protein beta	STRADB ALS2CR2 ILPIP	2	1
B3KWK7	Insulin like growth factor binding protein 3	IGFBP3	2	0
P48552	Nuclear receptor-interacting protein 1	NRIP1	2	1
Q7Z3S9	Notch homolog 2 N-terminal-like protein A	NOTCH2NLA N2N NOTCH2NL	2	1
Q9BXU1	Serine/threonine-protein kinase 31	STK31 SGK396	2	1
P31146	Coronin-1A	CORO1A CORO1	2	1

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