GlyCosmos Portal

Displaying entries **3401 - 3425** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q2KHM9	Protein moonraker	KIAA0753 MNR OFIP	0	1
Q9BTP7	Fanconi anemia core complex-associated protein 24	FAAP24 C19orf40	0	1
Q8IVF5	Rho guanine nucleotide exchange factor TIAM2	TIAM2 KIAA2016 STEF	0	1
Q6ZN17	Protein lin-28 homolog B	LIN28B CSDD2	0	1
Q9UBQ5	Eukaryotic translation initiation factor 3 subunit K	EIF3K EIF3S12	0	1
Q96JJ6	Junctophilin-4	JPH4 JPHL1 KIAA1831	0	1
Q9H0K1	Serine/threonine-protein kinase SIK2	SIK2 KIAA0781 QIK SNF1LK2	0	1
Q13162	Peroxiredoxin-4	PRDX4	0	1
P40126	L-dopachrome tautomerase	DCT TYRP2	6	1
Q66PJ3	ADP-ribosylation factor-like protein 6-interacting protein 4	ARL6IP4	0	1
Q8NBR9	Uncharacterized protein NDUFV1-DT	NDUFV1-DT C11orf72	0	1
A4D1E1	Zinc finger protein 804B	ZNF804B	0	1
Q9BT22	Chitobiosyldiphosphodolichol beta-mannosyltransferase	ALG1 HMAT1 HMT1	0	1	B-cell lymphoma Cauda equina syndrome Creutzfeldt-Jakob disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Walker-Warburg syndrome amyotrophic lateral sclerosis type 1 breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cerebral degeneration cerebral infarction cerebrovascular disease colon cancer colonic benign neoplasm congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 diabetes mellitus endomyocardial fibrosis enophthalmos epilepsy familial hypertrophic cardiomyopathy familial nephrotic syndrome focal epilepsy glomerulonephritis goiter hepatocellular carcinoma hyperthyroidism hypertrophic cardiomyopathy hypogonadism kidney disease laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoma malignant pleural mesothelioma microcephaly nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome neurogenic bladder nodular goiter obsolete exophthalmos obsolete ymphosarcoma orbital disease partial motor epilepsy placental insufficiency pyoureter reticulosarcoma schizophrenia scoliosis systemic lupus erythematosus thyroid gland disease thyrotoxicosis type 2 diabetes mellitus urinary tract obstruction visual epilepsy
Q7Z6P3	Ras-related protein Rab-44	RAB44	1	1
Q17RB8	LON peptidase N-terminal domain and RING finger protein 1	LONRF1 RNF191	1	1
Q6H8Q1	Actin-binding LIM protein 2	ABLIM2 KIAA1808	6	1
Q9UHV5	Rap guanine nucleotide exchange factor-like 1	RAPGEFL1	3	1
Q93062	RNA-binding protein with multiple splicing	RBPMS HERMES	0	1
Q13401	Putative postmeiotic segregation increased 2-like protein 3	PMS2P3 PMS2L3 PMS2L9 PMS5 PMSR3	0	1
Q4G0X4	BTB/POZ domain-containing protein KCTD21	KCTD21	0	1
Q9Y2T1	Axin-2	AXIN2	0	1
Q9H4A4	Aminopeptidase B	RNPEP APB	2	1
Q5VTL8	Pre-mRNA-splicing factor 38B	PRPF38B	0	1
Q9BTN0	Leucine-rich repeat and fibronectin type-III domain-containing protein 3	LRFN3 SALM4	5	1
Q9NVV2	Putative uncharacterized protein C19orf73	C19orf73	0	1

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