GlyCosmos Portal

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The O-GlcNAc Database	June 3, 2024
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Displaying entries **111076 - 111100** 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
P12960	Contactin-1	Cntn1	Mus musculus (house mouse)	10	27
Q28106	Contactin-1	CNTN1	Bos taurus (cattle)	8	0
H2KZ60	Contactin rig-6	rig-6	Caenorhabditis elegans	13	0
D3YWB9	Contactin associated protein-like 4	Cntnap4	Mus musculus (house mouse)	2	0
E9QNF7	Contactin associated protein-like 2	Cntnap2	Mus musculus (house mouse)	7	0
E0CXE3	Contactin 6	Cntn6	Mus musculus (house mouse)	2	0
F8WH58	Contactin 4	Cntn4	Mus musculus (house mouse)	1	0
A0A087WQQ9	Contactin 2 (Fragment)	Cntn2	Mus musculus (house mouse)	2	0
A0A087WPI9	Contactin 2 (Fragment)	Cntn2	Mus musculus (house mouse)	1	0
Q9VN14	Contactin	Cont	Drosophila melanogaster (fruit fly)	12	0
P08796	Contact site A protein	csaA	Dictyostelium discoideum	5	0
Q9NZB2	Constitutive coactivator of PPAR-gamma-like protein 1	FAM120A C9orf10 KIAA0183 OSSA	Homo sapiens (human)	1	2
Q6A0A9	Constitutive coactivator of PPAR-gamma-like protein 1	FAM120A Kiaa0183 Ossa	Mus musculus (house mouse)	1	2
P24031	Constitutive acid phosphatase	PHO3	Saccharomyces cerevisiae S288C	12	0
O45879	Conserved plasma membrane protein	mnr-1	Caenorhabditis elegans	1	0
Q96MW5	Conserved oligomeric Golgi complex subunit 8	COG8	Homo sapiens (human)	1	1	Dandy-Walker syndrome Unverricht-Lundborg syndrome alternating esotropia alveolar soft part sarcoma blepharospasm brain disease clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIh congenital disorder of glycosylation developmental and epileptic encephalopathy 36 early myoclonic encephalopathy epilepsy esophageal cancer esophageal carcinoma focal hand dystonia hepatocellular carcinoma hydrocephalus hypoglycemia intellectual disability isolated elevated serum creatine phosphokinase levels large intestine cancer learning disability liver cancer lung benign neoplasm lung carcinoma microcephaly protein-losing enteropathy scoliosis status epilepticus stomach cancer stomach carcinoma visual epilepsy
Q4D9M6	Conserved oligomeric Golgi complex subunit 7	Tc00.1047053503723.80	Trypanosoma cruzi strain CL Brener	0	1
P83436	Conserved oligomeric Golgi complex subunit 7	COG7	Homo sapiens (human)	1	1	Cauda equina syndrome Laron syndrome achondroplasia autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis cardiomyopathy cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIe congenital disorder of glycosylation congenital heart disease congestive heart failure endomyocardial fibrosis esophagitis familial hypertrophic cardiomyopathy gastroesophageal reflux disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels microcephaly neurogenic bladder obsolete congenital ichthyosiform erythroderma peptic esophagitis placental insufficiency sensorineural hearing loss
Q8R3I3	Conserved oligomeric Golgi complex subunit 6	Cog6 Kiaa1134	Mus musculus (house mouse)	0	1
A0A0R4J0L5	Conserved oligomeric Golgi complex subunit 6	Cog6	Mus musculus (house mouse)	0	1
U4U057	Conserved oligomeric Golgi complex subunit 6	D910_04656	Dendroctonus ponderosae (mountain pine beetle)	2	0
Q9Y2V7	Conserved oligomeric Golgi complex subunit 6	COG6 KIAA1134	Homo sapiens (human)	2	1	Gilbert syndrome acquired hyperkeratosis allergic asthma anemia anhidrosis asthma bilirubin metabolic disorder blood coagulation disease cerebral degeneration cholestasis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIl congenital disorder of glycosylation coronary artery disease dental caries dental enamel hypoplasia dentin caries developmental and epileptic encephalopathy 36 epilepsy gastroenteritis gastrointestinal system disease hydrocephalus hypohidrosis intellectual disability intestinal disease intrinsic asthma juvenile rheumatoid arthritis learning disability leiomyoma macrocytic anemia microcephaly myofibroma nonepidermolytic palmoplantar keratoderma palmoplantar keratosis pancytopenia parapsoriasis placental insufficiency primary biliary cholangitis primary immunodeficiency disease proctitis psoriasis pustulosis of palm and sole rheumatoid arthritis systemic lupus erythematosus thrombocytopenia uterine fibroid visual epilepsy
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
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
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

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