GlyCosmos Portal

Displaying entries **1976 - 2000** of **18496** in total

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9HC73	Cytokine receptor-like factor 2	CRLF2 CRL2 ILXR TSLPR	4	1
Q9HC58	Sodium/potassium/calcium exchanger 3	SLC24A3 NCKX3	4	1
Q9HC56	Protocadherin-9	PCDH9	15	22
Q9HC52	Chromobox protein homolog 8	CBX8 PC3 RC1	1	2
Q9HC44	Vasculin-like protein 1	GPBP1L1	0	1
Q9HC38	Glyoxalase domain-containing protein 4	GLOD4 C17orf25	0	1
Q9HC36	rRNA methyltransferase 3, mitochondrial	MRM3 RNMTL1	1	1
Q9HC35	Echinoderm microtubule-associated protein-like 4	EML4 C2orf2 EMAPL4	2	1
Q9HC29	Nucleotide-binding oligomerization domain-containing protein 2	NOD2 CARD15	0	1
Q9HC21	Mitochondrial thiamine pyrophosphate carrier	SLC25A19 DNC MUP1	1	2
Q9HC07	Putative divalent cation/proton antiporter TMEM165	TMEM165 TPARL	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
Q9HBZ2	Aryl hydrocarbon receptor nuclear translocator 2	ARNT2 BHLHE1 KIAA0307	0	1
Q9HBY0	NADPH oxidase 3	NOX3 MOX2	2	0
Q9HBX9	Relaxin receptor 1	RXFP1 LGR7	6	0
Q9HBX8	Leucine-rich repeat-containing G-protein coupled receptor 6	LGR6	2	0
Q9HBW9	Adhesion G protein-coupled receptor L4	ADGRL4 ELTD1 ETL	11	31
Q9HBW1	Leucine-rich repeat-containing protein 4	LRRC4 BAG	9	1
Q9HBW0	Lysophosphatidic acid receptor 2	LPAR2 EDG4 LPA2	2	0
Q9HBV2	Sperm acrosome membrane-associated protein 1	SPACA1 SAMP32	1	0
Q9HBV1	Popeye domain-containing protein 3	POPDC3 POP3	1	0
Q9HBU9	Popeye domain-containing protein 2	POPDC2 POP2	1	1
Q9HBU6	Ethanolamine kinase 1	ETNK1 EKI1	2	2	aggressive systemic mastocytosis atypical chronic myeloid leukemia, BCR-ABL1 negative cancer chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia disseminated eosinophilic collagen disease hypereosinophilic syndrome indolent systemic mastocytosis juvenile myelomonocytic leukemia mastocytosis myeloid leukemia obsolete subacute myeloid leukemia seminoma systemic mastocytosis testicular cancer testicular germ cell cancer testis seminoma
Q9HBT8	Zinc finger protein 286A	ZNF286A KIAA1874 ZNF286	0	1
Q9HBT6	Cadherin-20	CDH20 CDH7L3	4	0
Q9HBR0	Solute carrier family 38 member 10	SLC38A10	24	2

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