GlyCosmos Portal

Displaying entries **16076 - 16100** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of GlyTouCan IDs	Disease Ontology
P14927	Cytochrome b-c1 complex subunit 7	UQCRB UQBP	1
P07148	Fatty acid-binding protein, liver	FABP1 FABPL	1
O14979	Heterogeneous nuclear ribonucleoprotein D-like	HNRNPDL HNRPDL JKTBP	1
Q96ER9	Mitochondrial potassium channel	CCDC51 MITOK	1
Q13164	Mitogen-activated protein kinase 7	MAPK7 BMK1 ERK5 PRKM7	1
Q8TDC3	Serine/threonine-protein kinase BRSK1	BRSK1 KIAA1811 SAD1 SADB	1
Q96I36	Cytochrome c oxidase assembly protein COX14	COX14 C12orf62	1
P53602	Diphosphomevalonate decarboxylase	MVD MPD	1
Q96CW6	Probable RNA polymerase II nuclear localization protein SLC7A6OS	SLC7A6OS	1
Q8WUY1	Protein THEM6	THEM6 C8orf55	1
Q92670	Putative zinc finger protein 75C	ZNF75CP ZNF75C	1
O43181	NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial	NDUFS4	1
Q96IU4	Putative protein-lysine deacylase ABHD14B	ABHD14B CIB	1
Q9UKT8	F-box/WD repeat-containing protein 2	FBXW2 FBW2 FWD2	1
Q5VUG0	Scm-like with four MBT domains protein 2	SFMBT2 KIAA1617	1
Q9HB07	MYG1 exonuclease	MYG1 C12orf10	1
Q969M3	Protein YIPF5	YIPF5 FINGER5 YIP1A	1
Q6ZW49	PAX-interacting protein 1	PAXIP1 PAXIP1L PTIP	1
Q9UPZ3	BLOC-2 complex member HPS5	HPS5 AIBP63 KIAA1017	1
Q8N7Z5	Ankyrin repeat domain-containing protein 31	ANKRD31	1
O94953	Lysine-specific demethylase 4B	KDM4B JHDM3B JMJD2B KIAA0876	1
Q9H444	Charged multivesicular body protein 4b	CHMP4B C20orf178 SHAX1	1
P37837	Transaldolase	TALDO1 TAL TALDO TALDOR	1	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease T-cell acute lymphoblastic leukemia acatalasia allergic asthma anemia asthma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer capillary disease childhood T-cell acute lymphoblastic leukemia childhood leukemia chronic kidney disease diabetes mellitus diabetic ketoacidosis disease of metabolism gallbladder disease head and neck squamous cell carcinoma hemangioma of liver hepatocellular carcinoma hereditary hemorrhagic telangiectasia immune system disease intrinsic asthma leukemia liver cancer liver cirrhosis liver disease macrocytic anemia multiple sclerosis obsolete T-cell lymphoblastic leukemia/lymphoma oligohydramnios osteomalacia pancytopenia patent ductus arteriosus patent foramen ovale placental insufficiency rickets sensorineural hearing loss sickle cell anemia skin benign neoplasm skin cancer squamous cell carcinoma telangiectasis thrombocytopenia tongue squamous cell carcinoma type 2 diabetes mellitus ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
P61165	Transmembrane protein 258	TMEM258 C11orf10	1
Q9Y5S9	RNA-binding protein 8A	RBM8A RBM8	1

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