GlyCosmos Portal

Displaying entries **17026 - 17050** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q99988	Growth/differentiation factor 15	GDF15 MIC1 PDF PLAB PTGFB	7	4
P09619	Platelet-derived growth factor receptor beta	PDGFRB PDGFR PDGFR1	11	4
Q9NXV6	CDKN2A-interacting protein	CDKN2AIP CARF	40	4
Q9UKP4	A disintegrin and metalloproteinase with thrombospondin motifs 7	ADAMTS7	21	4
P07204	Thrombomodulin	THBD THRM	8	4
P19397	Leukocyte surface antigen CD53	CD53 MOX44 TSPAN25	2	4
Q6ZVL6	UPF0606 protein KIAA1549L	KIAA1549L C11orf41 C11orf69	16	4
P31930	Cytochrome b-c1 complex subunit 1, mitochondrial	UQCRC1	1	4
Q8NDX5	Polyhomeotic-like protein 3	PHC3 EDR3 PH3	24	4
Q09666	Neuroblast differentiation-associated protein AHNAK	AHNAK PM227	112	4
Q86XS8	E3 ubiquitin-protein ligase RNF130	RNF130	6	4
Q9Y2Z0	Protein SGT1 homolog	SUGT1	2	4
O95428	Papilin	PAPLN	22	4
P14222	Perforin-1	PRF1 PFP	2	4
P42695	Condensin-2 complex subunit D3	NCAPD3 CAPD3 KIAA0056	4	4
Q9UKM7	Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase	MAN1B1	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
Q2VWP7	Protogenin	PRTG	7	4
P57087	Junctional adhesion molecule B	JAM2 C21orf43 VEJAM	3	4
P10747	T-cell-specific surface glycoprotein CD28	CD28	5	4
Q7KZI7	Serine/threonine-protein kinase MARK2	MARK2 EMK1	4	4
Q9BY12	S phase cyclin A-associated protein in the endoplasmic reticulum	SCAPER KIAA1454 ZNF291	3	4
P08476	Inhibin beta A chain	INHBA	5	4
Q9GZP0	Platelet-derived growth factor D	PDGFD IEGF SCDGFB	5	4
Q86VM9	Zinc finger CCCH domain-containing protein 18	ZC3H18 NHN1	3	4
Q9H497	Torsin-3A	TOR3A ADIR	2	4

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