GlyCosmos Portal

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Displaying entries **114326 - 114350** 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
P17676	CCAAT/enhancer-binding protein beta	CEBPB TCF5	Homo sapiens (human)	2	1
Q6XZF7	Dynamin-binding protein	DNMBP ARHGEF36 KIAA1010 TUBA	Homo sapiens (human)	1	1
P38983	Small ribosomal subunit protein uS2	Rpsa Lamr1	Rattus norvegicus (Norway rat)	0	1
Q9NQR8	NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 4	Ndufaf4 Hrpap20	Rattus norvegicus (Norway rat)	1	1
M9NCQ1	Uncharacterized protein, isoform B	Dmel\CG31663 BcDNA:GH27779 CG15359 CG15360	Drosophila melanogaster (fruit fly)	0	1
Q96B23	Protein ARK2N	ARK2N ARKL1 C18orf25	Homo sapiens (human)	2	1
Q9W111	Epidermal growth factor receptor pathway substrate clone 15, isoform A	Eps-15 Aa2/2 Dmel\CG16932 EH1 EPS-15 EPS15 Eps15 anon-WO0118547.85 eps-15 eps15 i31	Drosophila melanogaster (fruit fly)	0	1
P35712	Transcription factor SOX-6	SOX6	Homo sapiens (human)	2	1
Q08018	Putative uncharacterized protein YLR076C	YLR076C	Saccharomyces cerevisiae S288C	0	1
Q7KSQ0	Citrate transport protein	sea CG31305 DmCIC Dmel\CG6782 SLC25A1 Sea anon-WO0140519.12 l(3)EP3364 sea[Delta24]	Drosophila melanogaster (fruit fly)	0	1
Q9CYQ7	Nuclear prelamin A recognition factor	Narf	Mus musculus (house mouse)	1	1
P35171	Cytochrome c oxidase subunit 7A2, mitochondrial	Cox7a2 Cox7a3 Cox7al	Rattus norvegicus (Norway rat)	1	1
A0A0A6YW67	Predicted pseudogene 8797	Gm8797	Mus musculus (house mouse)	0	1
Q924X2	Carnitine O-palmitoyltransferase 1, muscle isoform	Cpt1b	Mus musculus (house mouse)	0	1
Q4D7D9	J domain-containing protein	Tc00.1047053510407.80	Trypanosoma cruzi strain CL Brener	0	1
Q03868	Prospore membrane adapter protein SPO71	SPO71	Saccharomyces cerevisiae S288C	4	1
V5BVR2	Pyrroline-5-carboxylate reductase	TCDM_02525	Trypanosoma cruzi Dm28c	0	1
V5BHV5	Pitrilysin-like metalloprotease	TCDM_07985	Trypanosoma cruzi Dm28c	0	1
P14148	Large ribosomal subunit protein uL30	Rpl7	Mus musculus (house mouse)	0	1
Q16836	Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial	HADH HAD HAD1 HADHSC SCHAD	Homo sapiens (human)	0	1	X-linked dilated cardiomyopathy Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction adrenoleukodystrophy agnosia cancer cardiomyopathy cone-rod dystrophy congestive heart failure coronary thrombosis developmental coordination disorder diabetes mellitus diarrhea dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism embryoma endomyocardial fibrosis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperinsulinemic hypoglycemia 4 familial hypertrophic cardiomyopathy fundus albipunctatus gallbladder disease hepatitis hyperinsulinemic hypoglycemia hyperinsulinism hypertrophic cardiomyopathy hypoglycemia hypoglycemic coma intellectual disability lactic acidosis laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver disease maple syrup urine disease mitochondrial trifunctional protein deficiency myocardial infarction myoglobinuria neuropathy obesity peripheral nervous system disease peroxisomal disease placental insufficiency retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus urea cycle disorder
P18480	SWI/SNF chromatin-remodeling complex subunit SNF5	SNF5 SWI10 TYE4	Saccharomyces cerevisiae S288C	3	1
Q4D0C0	NADH-cytochrome b5 reductase	Tc00.1047053511047.40	Trypanosoma cruzi strain CL Brener	0	1
Q4CXR9	Cystathionine beta-synthase	Tc00.1047053506905.50	Trypanosoma cruzi strain CL Brener	0	1
V5B825	Monooxygenase	TCDM_01938	Trypanosoma cruzi Dm28c	0	1
Q4CVE1	Plectin	Tc00.1047053507933.10	Trypanosoma cruzi strain CL Brener	0	1

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