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 **16501 - 16525** 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
Q9HBU9	Popeye domain-containing protein 2	POPDC2 POP2	Homo sapiens (human)	1	1
Q9HBV1	Popeye domain-containing protein 3	POPDC3 POP3	Homo sapiens (human)	1	0
Q9HBV2	Sperm acrosome membrane-associated protein 1	SPACA1 SAMP32	Homo sapiens (human)	1	0
Q9HBW0	Lysophosphatidic acid receptor 2	LPAR2 EDG4 LPA2	Homo sapiens (human)	2	0
Q9HBW1	Leucine-rich repeat-containing protein 4	LRRC4 BAG	Homo sapiens (human)	9	1
Q9HBW9	Adhesion G protein-coupled receptor L4	ADGRL4 ELTD1 ETL	Homo sapiens (human)	11	31
Q9HBX8	Leucine-rich repeat-containing G-protein coupled receptor 6	LGR6	Homo sapiens (human)	2	0
Q9HBX9	Relaxin receptor 1	RXFP1 LGR7	Homo sapiens (human)	6	0
Q9HBY0	NADPH oxidase 3	NOX3 MOX2	Homo sapiens (human)	2	0
Q9HBZ2	Aryl hydrocarbon receptor nuclear translocator 2	ARNT2 BHLHE1 KIAA0307	Homo sapiens (human)	0	1
Q9HC07	Putative divalent cation/proton antiporter TMEM165	TMEM165 TPARL	Homo sapiens (human)	4	3	Camurati-Engelmann disease Laron syndrome Marfan syndrome X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 achondroplasia acoustic neuroma amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta cancer cellular schwannoma chondrodysplasia punctata congenital disorder of glycosylation type II congenital disorder of glycosylation type IIk congenital disorder of glycosylation dentin dysplasia dentinogenesis imperfecta embryoma hepatocellular carcinoma isolated elevated serum creatine phosphokinase levels liver cancer melanotic neurilemmoma meningioma neurilemmoma neurofibromatosis osteoporosis pituitary adenoma plexiform schwannoma scoliosis situs inversus tuberous sclerosis vestibular schwannomatosis
Q9HC21	Mitochondrial thiamine pyrophosphate carrier	SLC25A19 DNC MUP1	Homo sapiens (human)	1	2
Q9HC29	Nucleotide-binding oligomerization domain-containing protein 2	NOD2 CARD15	Homo sapiens (human)	0	1
Q9HC35	Echinoderm microtubule-associated protein-like 4	EML4 C2orf2 EMAPL4	Homo sapiens (human)	2	1
Q9HC36	rRNA methyltransferase 3, mitochondrial	MRM3 RNMTL1	Homo sapiens (human)	1	1
Q9HC38	Glyoxalase domain-containing protein 4	GLOD4 C17orf25	Homo sapiens (human)	0	1
Q9HC44	Vasculin-like protein 1	GPBP1L1	Homo sapiens (human)	0	1
Q9HC52	Chromobox protein homolog 8	CBX8 PC3 RC1	Homo sapiens (human)	1	2
Q9HC56	Protocadherin-9	PCDH9	Homo sapiens (human)	15	22
Q9HC58	Sodium/potassium/calcium exchanger 3	SLC24A3 NCKX3	Homo sapiens (human)	4	1
Q9HC73	Cytokine receptor-like factor 2	CRLF2 CRL2 ILXR TSLPR	Homo sapiens (human)	4	1
Q9HC77	Centromere protein J	CENPJ CPAP LAP LIP1	Homo sapiens (human)	0	1
Q9HC78	Zinc finger and BTB domain-containing protein 20	ZBTB20 DPZF ZNF288	Homo sapiens (human)	11	2
Q9HC84	Mucin-5B	MUC5B MUC5	Homo sapiens (human)	54	47
Q9HC96	Calpain-10	CAPN10 KIAA1845	Homo sapiens (human)	1	1

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