GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **15901 - 15925** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
H0Y991	Collagen type XII alpha 1 chain (Fragment)	COL12A1	Homo sapiens (human)	1	0
B9EJB8	Collagen, type XII, alpha 1	COL12A1	Homo sapiens (human)	2	0
Q99715	Collagen alpha-1(XII) chain	COL12A1 COL12A1L	Homo sapiens (human)	31	130
P13942	Collagen alpha-2(XI) chain	COL11A2	Homo sapiens (human)	3	1
P12107	Collagen alpha-1(XI) chain	COL11A1 COLL6	Homo sapiens (human)	8	4
Q03692	Collagen alpha-1(X) chain	COL10A1	Homo sapiens (human)	6	1
P38432	Coilin	COIL CLN80	Homo sapiens (human)	0	1
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
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
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
G3V5V4	Cochlin (Fragment)	COCH	Homo sapiens (human)	1	0
A0A2U3TZE7	Cochlin	COCH	Homo sapiens (human)	1	0
A0A2R8Y3T0	Cochlin	COCH	Homo sapiens (human)	1	0
O43405	Cochlin	COCH COCH5B2	Homo sapiens (human)	8	9
O75128	Protein cordon-bleu	COBL KIAA0633	Homo sapiens (human)	0	1
Q13057	Bifunctional coenzyme A synthase	COASY	Homo sapiens (human)	0	1
Q96BR5	Cytochrome c oxidase assembly factor 7	COA7 C1orf163 RESA1 SELRC1	Homo sapiens (human)	0	1
Q5JTJ3	Cytochrome c oxidase assembly factor 6 homolog	COA6 C1orf31	Homo sapiens (human)	2	1
Q8N137	Centrobin	CNTROB LIP8	Homo sapiens (human)	1	1
Q7Z7A1	Centriolin	CNTRL CEP1 CEP110	Homo sapiens (human)	0	1
Q8WYK1	Contactin-associated protein-like 5	CNTNAP5 CASPR5	Homo sapiens (human)	5	0
Q9C0A0	Contactin-associated protein-like 4	CNTNAP4 CASPR4 KIAA1763	Homo sapiens (human)	12	0

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