GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
Q9NSA0	Solute carrier family 22 member 11	SLC22A11 OAT4	3	0
Q12768	WASH complex subunit 5	WASHC5 KIAA0196	3	1
Q9UM44	HERV-H LTR-associating protein 2	HHLA2	3	1
Q13243	Serine/arginine-rich splicing factor 5	SRSF5 HRS SFRS5 SRP40	3	1
Q9Y243	RAC-gamma serine/threonine-protein kinase	AKT3 PKBG	3	1
O75439	Mitochondrial-processing peptidase subunit beta	PMPCB MPPB	3	1
O43159	Ribosomal RNA-processing protein 8	RRP8 KIAA0409 NML	3	1
A0A7I6GV05	Complement factor B (Fragment)	Bf	3	0
P41968	Melanocortin receptor 3	MC3R	3	0
Q86XE5	4-hydroxy-2-oxoglutarate aldolase, mitochondrial	HOGA1 C10orf65 DHDPSL	3	1	calcinosis calcium metabolism disease cholestasis chronic kidney disease hypercalcemia nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria
P31274	Homeobox protein Hox-C9	HOXC9 HOX3B	3	1
Q9GZX6	Interleukin-22	IL22 ILTIF ZCYTO18	3	0
G1JTE6	MHC class I chain-related protein A (Fragment)	MICA	3	0
P51553	Isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial	IDH3G	3	1
J9UPX7	MHC Class I chain-related protein	MICA	3	0
P42704	Leucine-rich PPR motif-containing protein, mitochondrial	LRPPRC LRP130	3	2
Q96LR9	Apolipoprotein L domain-containing protein 1	APOLD1 VERGE	3	1
Q11203	CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase	ST3GAL3 SIAT6	3	3	Unverricht-Lundborg syndrome West syndrome agnosia amyotrophic lateral sclerosis attention deficit hyperactivity disorder autosomal recessive intellectual developmental disorder 12 autosomal recessive intellectual developmental disorder bipolar disorder blepharospasm brain cancer breast cancer breast carcinoma cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma choreatic disease congenital disorder of glycosylation depressive disorder developmental and epileptic encephalopathy 15 developmental coordination disorder diabetes mellitus dysthymic disorder dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy focal epilepsy focal hand dystonia hepatocellular carcinoma influenza intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia pancreatic adenocarcinoma partial motor epilepsy progressive muscular atrophy prostate cancer prostate carcinoma pterygium schizophrenia stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
F1BE19	MHC class I polypeptide-related protein A (Fragment)	MICA	3	0
P35236	Tyrosine-protein phosphatase non-receptor type 7	PTPN7	3	1
O75027	Iron-sulfur clusters transporter ABCB7, mitochondrial	ABCB7 ABC7	3	1
A0A7P0TA85	Basigin	BSG	3	0
Q13477	Mucosal addressin cell adhesion molecule 1	MADCAM1	3	2
Q13557	Calcium/calmodulin-dependent protein kinase type II subunit delta	CAMK2D CAMKD	3	1
O43516	WAS/WASL-interacting protein family member 1	WIPF1 WASPIP WIP	3	2

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