GlyCosmos Portal

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Displaying entries **115126 - 115150** 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
Q8RXN9	Putative beta-glucosidase 5	BGLU5	Arabidopsis thaliana (thale cress)	5	0
A0A336U966	Tyrosinase P	tyrP	Aspergillus terreus	5	0
Q6NY73	Galectin-3-binding protein B	lgals3bpb	Danio rerio (zebrafish)	5	0
F5H094	SLCO1B3-SLCO1B7 readthrough transcript protein	SLCO1B3-SLCO1B7	Homo sapiens (human)	5	0
P30639	Protein linkin	lnkn-1 tag-256	Caenorhabditis elegans	5	0
Q65Z14	Oncostatin-M-specific receptor subunit beta	Osmr Osmrb	Rattus norvegicus (Norway rat)	5	0
Q06568	Nuclear distribution protein nudE homolog 1	NDL1	Saccharomyces cerevisiae S288C	5	1
Q07959	ADIPOR-like receptor IZH3	IZH3	Saccharomyces cerevisiae S288C	5	0
Q28832	Low-density lipoprotein receptor (Fragment)	LDLR	Sus scrofa (pig)	5	0
Q96RQ9	L-amino-acid oxidase	IL4I1 FIG1	Homo sapiens (human)	5	16
P40066	mRNA export factor GLE2	GLE2 RAE1	Saccharomyces cerevisiae S288C	5	1
Q9DBY4	TLR4 interactor with leucine rich repeats	Tril Kiaa0644	Mus musculus (house mouse)	5	4
Q25263	Receptor-type adenylate cyclase B	RAC-B	Leishmania donovani	5	0
P58242	Acid sphingomyelinase-like phosphodiesterase 3b	Smpdl3b Asml3b	Mus musculus (house mouse)	5	3
Q9DCP2	Sodium-coupled neutral amino acid transporter 3	Slc38a3 Sn1 Snat3	Mus musculus (house mouse)	5	2
Q9Y487	V-type proton ATPase 116 kDa subunit a 2	ATP6V0A2	Homo sapiens (human)	5	7	Crohn's colitis Crohn's disease Dandy-Walker syndrome Ehlers-Danlos syndrome Hailey-Hailey disease Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Rothmund-Thomson syndrome achondroplasia agnosia alopecia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 autosomal recessive osteopetrosis 7 bacterial sepsis bicuspid aortic valve disease bone disease breast cancer breast carcinoma cancer cartilage disease clubfoot complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease coronary artery disease cortical dysplasia-focal epilepsy syndrome cryptococcosis cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder diabetic cataract diabetic retinopathy encephalitis encephalomyelitis epilepsy essential hypertension generalized atherosclerosis geroderma osteodysplasticum giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hydranencephaly hypertension hypertropia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intracranial aneurysm learning disability lipoatrophic diabetes mellitus lipodystrophy lissencephaly lung disease mal de Meleda male infertility mechanical strabismus microcephaly mixed glioma myelitis myopia omphalocele ophthalmoplegia osteogenesis imperfecta osteopetrosis osteosclerosis placental insufficiency platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pulmonary emphysema renal tubular acidosis restrictive dermopathy scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly status epilepticus strabismus syndromic X-linked intellectual disability Najm type ulcerative colitis umbilical hernia visual epilepsy von Willebrand's disease
A0A0G2JDH9	Prominin 1	Prom1	Mus musculus (house mouse)	5	0
Q9P2D6	Protein FAM135A	FAM135A KIAA1411	Homo sapiens (human)	5	3
P08049	Neprilysin	MME	Oryctolagus cuniculus (rabbit)	5	0
Q6CW36	GPI ethanolamine phosphate transferase 1	MCD4	Kluyveromyces lactis NRRL Y-1140	5	0
Q8LPK2	ABC transporter B family member 2	ABCB2 MDR2 PGP2	Arabidopsis thaliana (thale cress)	5	0
B8NMK3	Extracellular metalloproteinase mep	mep	Aspergillus flavus NRRL3357	5	0
P16721	Protein UL11	UL11	Human herpesvirus 5 strain AD169	5	0
Q9ERS6	X-linked interleukin-1 receptor accessory protein-like 2	Il1rapl2	Mus musculus (house mouse)	5	0
Q04857	Collagen alpha-1(VI) chain	Col6a1	Mus musculus (house mouse)	5	17

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