GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **14026 - 14050** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q9Y243	RAC-gamma serine/threonine-protein kinase	AKT3 PKBG	Homo sapiens (human)	3	1
O75439	Mitochondrial-processing peptidase subunit beta	PMPCB MPPB	Homo sapiens (human)	3	1
O43159	Ribosomal RNA-processing protein 8	RRP8 KIAA0409 NML	Homo sapiens (human)	3	1
A0A7I6GV05	Complement factor B (Fragment)	Bf	Homo sapiens (human)	3	0
P41968	Melanocortin receptor 3	MC3R	Homo sapiens (human)	3	0
Q86XE5	4-hydroxy-2-oxoglutarate aldolase, mitochondrial	HOGA1 C10orf65 DHDPSL	Homo sapiens (human)	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	Homo sapiens (human)	3	1
Q9GZX6	Interleukin-22	IL22 ILTIF ZCYTO18	Homo sapiens (human)	3	0
G1JTE6	MHC class I chain-related protein A (Fragment)	MICA	Homo sapiens (human)	3	0
P51553	Isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial	IDH3G	Homo sapiens (human)	3	1
J9UPX7	MHC Class I chain-related protein	MICA	Homo sapiens (human)	3	0
P42704	Leucine-rich PPR motif-containing protein, mitochondrial	LRPPRC LRP130	Homo sapiens (human)	3	2
Q96LR9	Apolipoprotein L domain-containing protein 1	APOLD1 VERGE	Homo sapiens (human)	3	1
Q11203	CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase	ST3GAL3 SIAT6	Homo sapiens (human)	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	Homo sapiens (human)	3	0
P35236	Tyrosine-protein phosphatase non-receptor type 7	PTPN7	Homo sapiens (human)	3	1
O75027	Iron-sulfur clusters transporter ABCB7, mitochondrial	ABCB7 ABC7	Homo sapiens (human)	3	1
A0A7P0TA85	Basigin	BSG	Homo sapiens (human)	3	0
Q13477	Mucosal addressin cell adhesion molecule 1	MADCAM1	Homo sapiens (human)	3	2
Q13557	Calcium/calmodulin-dependent protein kinase type II subunit delta	CAMK2D CAMKD	Homo sapiens (human)	3	1
O43516	WAS/WASL-interacting protein family member 1	WIPF1 WASPIP WIP	Homo sapiens (human)	3	2
O95858	Tetraspanin-15	TSPAN15 NET7 TM4SF15	Homo sapiens (human)	3	3
A0A7I2V3B5	ADAM metallopeptidase domain 9	ADAM9	Homo sapiens (human)	3	0
Q4ZG55	Protein GREB1	GREB1 KIAA0575	Homo sapiens (human)	3	1
Q5U651	Ras-interacting protein 1	RASIP1	Homo sapiens (human)	3	1

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