GlyCosmos Portal

Displaying entries **76 - 100** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of GlyTouCan IDs	Disease Ontology
Q8WUY8	Probable N-acetyltransferase 14	NAT14 KLP1	1
Q149N8	E3 ubiquitin-protein ligase SHPRH	SHPRH KIAA2023	1
Q8N8E3	Centrosomal protein of 112 kDa	CEP112 CCDC46	1
Q9UKS6	Protein kinase C and casein kinase substrate in neurons protein 3	PACSIN3	1
O43837	Isocitrate dehydrogenase [NAD] subunit beta, mitochondrial	IDH3B	1	Zollinger-Ellison syndrome bipolar disorder blindness cataract cone-rod dystrophy congenital nystagmus corneal disease diabetes mellitus dissociated nystagmus eye disease fundus albipunctatus fundus dystrophy glaucoma hidradenitis suppurativa hidradenitis hyperinsulinism hypogonadism intellectual disability keratoconus learning disability obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus pompholyx retinitis pigmentosa 46 retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus stomach cancer stomach carcinoma type 2 diabetes mellitus
Q14934	Nuclear factor of activated T-cells, cytoplasmic 4	NFATC4 NFAT3	1
Q99471	Prefoldin subunit 5	PFDN5 MM1 PFD5	1
Q00536	Cyclin-dependent kinase 16	CDK16 PCTAIRE1 PCTK1	1
Q99814	Endothelial PAS domain-containing protein 1	EPAS1 BHLHE73 HIF2A MOP2 PASD2	1
Q3MHD2	Protein LSM12	LSM12	1
P0DMB2	Uncharacterized protein C8orf88	C8orf88	1
Q9ULV3	Cip1-interacting zinc finger protein	CIZ1 LSFR1 NP94 ZNF356	1
Q9H0B3	IQ domain-containing protein N	IQCN KIAA1683	1
F1JVV5	EWSR1/ATF1 fusion protein type 1	EWSR1/ATF1 fusion	1
O14745	Na(+)/H(+) exchange regulatory cofactor NHE-RF1	NHERF1 NHERF SLC9A3R1	1
Q9NPD8	Ubiquitin-conjugating enzyme E2 T	UBE2T	1
E7EVA0	Microtubule-associated protein	MAP4	1
Q16720	Plasma membrane calcium-transporting ATPase 3	ATP2B3	1
Q15019	Septin-2	SEPTIN2 DIFF6 KIAA0158 NEDD5 SEPT2	1
O00221	NF-kappa-B inhibitor epsilon	NFKBIE IKBE	1
O75528	Transcriptional adapter 3	TADA3 ADA3 TADA3L	1
Q96M94	Kelch-like protein 15	KLHL15 KIAA1677	1
Q6B0I6	Lysine-specific demethylase 4D	KDM4D JHDM3D JMJD2D	1
Q969G6	Riboflavin kinase	RFK	1
P48449	Lanosterol synthase	LSS OSC	1	Baraitser-Winter syndrome Fabry disease Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Q fever Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome Wolman disease acquired immunodeficiency syndrome acute lymphoblastic leukemia adult acute lymphocytic leukemia alopecia ankylosing spondylitis arteriosclerotic cardiovascular disease atherosclerosis blindness bone osteosarcoma branchiootic syndrome breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract central nervous system cancer childhood acute lymphocytic leukemia childhood osteosarcoma chylomicron retention disease coronary artery disease diffuse idiopathic skeletal hyperostosis embryoma endometrial serous adenocarcinoma epilepsy epithelioid sarcoma essential hypertension giant cell glioblastoma glioblastoma gliosarcoma high grade glioma holoprosencephaly 1 holoprosencephaly human immunodeficiency virus infectious disease hypertension hypotrichosis 14 hypotrichosis 1 hypotrichosis intellectual disability learning disability lipid storage disease microcephaly mixed glioma orofaciodigital syndrome I orofaciodigital syndrome X ossification of the posterior longitudinal ligament of spine osteosarcoma ovary serous adenocarcinoma primary sclerosing cholangitis sarcoma sclerosing cholangitis senile cataract skin disease spinal stenosis spindle cell sarcoma squamous cell carcinoma tongue cancer tongue squamous cell carcinoma trypanosomiasis typhus visual epilepsy

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