GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **15426 - 15450** 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
Q6ZQK0	Condensin-2 complex subunit D3	Ncapd3 Kiaa0056	Mus musculus (house mouse)	2	2
Q6DFV1	Condensin-2 complex subunit G2	Ncapg2 Luzp5 Mtb	Mus musculus (house mouse)	1	1
Q86XI2	Condensin-2 complex subunit G2	NCAPG2 LUZP5	Homo sapiens (human)	1	1
Q6IBW4	Condensin-2 complex subunit H2	NCAPH2 CAPH2	Homo sapiens (human)	0	1
Q8BSP2	Condensin-2 complex subunit H2	Ncaph2 D15Ertd785e	Mus musculus (house mouse)	0	1
E9PY48	Condensin-2 complex subunit H2	Ncaph2	Mus musculus (house mouse)	0	1
P34090	Conditioned medium factor	cmfA	Dictyostelium discoideum	4	0
F5B8V6	Conglutin alpha 1	CONALPHA	Lupinus angustifolius (narrow-leaved blue lupine)	2	0
F5B8V9	Conglutin beta 1	BETA1	Lupinus angustifolius (narrow-leaved blue lupine)	2	0
F5B8W0	Conglutin beta 2	BETA2	Lupinus angustifolius (narrow-leaved blue lupine)	1	0
F5B8W1	Conglutin beta 3	BETA3	Lupinus angustifolius (narrow-leaved blue lupine)	2	0
F5B8W2	Conglutin beta 4	BETA4	Lupinus angustifolius (narrow-leaved blue lupine)	2	0
F5B8W3	Conglutin beta 5	BETA5	Lupinus angustifolius (narrow-leaved blue lupine)	1	0
F5B8W4	Conglutin beta 6	BETA6	Lupinus angustifolius (narrow-leaved blue lupine)	2	0
F5B8W5	Conglutin beta 7	BETA7	Lupinus angustifolius (narrow-leaved blue lupine)	2	0
P23805	Conglutinin	CGN1	Bos taurus (cattle)	1	0
Q7S936	Conidial surface nicotinamide adenine dinucleotide glycohydrolase	NCU07948	Neurospora crassa OR74A	4	0
Q4WL81	Conidial surface nicotinamide adenine dinucleotide glycohydrolase nadA	nadA	Aspergillus fumigatus Af293	3	0
Q8WXI2	Connector enhancer of kinase suppressor of ras 2	CNKSR2 CNK2 KIAA0902 KSR2	Homo sapiens (human)	2	1
Q80YA9	Connector enhancer of kinase suppressor of ras 2	Cnksr2 Kiaa0902	Mus musculus (house mouse)	6	1
Q8DWU4	Conserved domain protein	SAG2119	Streptococcus agalactiae 2603V/R	1	0
Q8WTW3	Conserved oligomeric Golgi complex subunit 1	COG1 KIAA1381 LDLB	Homo sapiens (human)	1	1	Baraitser-Winter syndrome Burkitt lymphoma Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Richter's syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome anemia branchiootic syndrome cerebral degeneration cerebrocostomandibular syndrome chronic lymphocytic leukemia clubfoot congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIg cryptorchidism hematologic cancer hydronephrosis hypospadias kidney failure macrocytic anemia orofaciodigital syndrome I orofaciodigital syndrome X placental insufficiency primary pulmonary hypertension scoliosis sensorineural hearing loss thrombocytopenia
Q9Z160	Conserved oligomeric Golgi complex subunit 1	Cog1 Ldlb	Mus musculus (house mouse)	0	1
Q96JB2	Conserved oligomeric Golgi complex subunit 3	COG3 SEC34	Homo sapiens (human)	3	1	autosomal recessive limb-girdle muscular dystrophy type 2A breast cancer cancer
Q9UP83	Conserved oligomeric Golgi complex subunit 5	COG5 GOLTC1 GTC90	Homo sapiens (human)	1	2	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Cauda equina syndrome Friedreich ataxia Laron syndrome Pick's disease Reye syndrome achondroplasia agnosia arthritis arthropathy atrial fibrillation cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIi congenital disorder of glycosylation coronary artery disease cryptorchidism developmental coordination disorder epilepsy hypertropia intellectual disability learning disability leiomyoma mechanical strabismus microcephaly myofibroma neurogenic bladder oligohydramnios ophthalmoplegia osteoarthritis placental insufficiency sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 uterine fibroid visual epilepsy

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