GlyCosmos Portal

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Displaying entries **125476 - 125500** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
P19070	Complement receptor type 2	Cr2	Mus musculus (house mouse)	17	0
Q9P8P2	Phospholipase B	PLB1	Cryptococcus neoformans var. grubii H99	17	0
Q9ZUI0	Putative leucine-rich repeat receptor-like serine/threonine-protein kinase At2g24130	At2g24130	Arabidopsis thaliana (thale cress)	17	0
E5RKB6	FELE-1	Stab1 FELE-1	Mus musculus (house mouse)	17	0
C0STH4	Probable exo-1,4-beta-xylosidase xlnD	xlnD xyl2 xylA	Aspergillus aculeatus	17	0
F4KHA2	Receptor-like protein 54	RLP54	Arabidopsis thaliana (thale cress)	17	0
Q62959	Leptin receptor	Lepr Fa Obr	Rattus norvegicus (Norway rat)	17	0
P23052	Spike glycoprotein	S P	Berne virus	17	0
Q96DR8	Mucin-like protein 1	MUCL1 SBEM	Homo sapiens (human)	17	1
Q9LS79	Receptor-like protein 38	RLP38	Arabidopsis thaliana (thale cress)	17	0
G7NS93	Toll-like receptor 7	EGK_20273	Macaca mulatta (Rhesus monkey)	17	0
Q61G93	Protein roller-3	rol-3	Caenorhabditis briggsae	17	0
Q70CT4	Receptor-like protein 8	RLP8 RPP27	Arabidopsis thaliana (thale cress)	17	0
P78527	DNA-dependent protein kinase catalytic subunit	PRKDC HYRC HYRC1	Homo sapiens (human)	17	7
Q9H4F8	SPARC-related modular calcium-binding protein 1	SMOC1	Homo sapiens (human)	17	9
Q9UKM7	Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase	MAN1B1	Homo sapiens (human)	17	4	Hailey-Hailey disease Rafiq syndrome Rothmund-Thomson syndrome agnosia alpha 1-antitrypsin deficiency autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bladder carcinoma bulimia nervosa cancer cerebral degeneration choreatic disease congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation cutis laxa depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease hepatocellular carcinoma hyperopia intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver disease major depressive disorder mal de Meleda melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia oophoritis parametritis partial motor epilepsy pelvic inflammatory disease periventricular nodular heterotopia pyosalpinx restrictive dermopathy salpingitis stereotypic movement disorder syndactyly syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 urinary bladder cancer visual epilepsy
P41832	Protein BNI1	BNI1 PPF3 SHE5	Saccharomyces cerevisiae S288C	17	1
Q8BYI9	Tenascin-R	Tnr	Mus musculus (house mouse)	17	50
Q9VUN0	Toll-like receptor 6	Toll-6 Tl-6	Drosophila melanogaster (fruit fly)	17	0
O14786	Neuropilin-1	NRP1 NRP VEGF165R	Homo sapiens (human)	17	58
O13854	Serine/threonine-rich protein adg2	adg2 mug46	Schizosaccharomyces pombe 972h-	17	0
O54991	Contactin-associated protein 1	Cntnap1 Nrxn4	Mus musculus (house mouse)	17	19
Q9NTZ6	RNA-binding protein 12	RBM12 KIAA0765	Homo sapiens (human)	17	3
Q9SLI6	Putative receptor-like protein 8	RLP8	Arabidopsis thaliana (thale cress)	17	0
Q9H1B7	Probable E3 ubiquitin-protein ligase IRF2BPL	IRF2BPL C14orf4 EAP1 KIAA1865	Homo sapiens (human)	17	3

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