GlyCosmos Portal

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Displaying entries **107551 - 107575** 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
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
P13944	Collagen alpha-1(XII) chain	COL12A1	Gallus gallus (chicken)	14	0
Q99715	Collagen alpha-1(XII) chain	COL12A1 COL12A1L	Homo sapiens (human)	31	130
Q32S24	Collagen alpha-2(XI) chain	COL11A2	Bos taurus (cattle)	2	0
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
A0A2G5B5I3	Calcium-dependent phosphotriesterase	COEREDRAFT_10500	Coemansia reversa NRRL 1564	1	0
I0YVE0	UDP-arabinopyranose mutase	COCSUDRAFT_24261	Coccomyxa subellipsoidea C-169	1	0
A0A9Q1CXA7	Potassium channel subfamily K member	COCON_G00226150	Conger conger (European conger)	1	0
A0A9Q1CWA8	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	COCON_G00222510	Conger conger (European conger)	1	0
A0A9Q1CZ00	Cathepsin D	COCON_G00219270	Conger conger (European conger)	2	0
A0A9Q1HQP3	Angiotensin-converting enzyme	COCON_G00211860	Conger conger (European conger)	2	0
A0A9Q1HPR6	Voltage-dependent P/Q-type calcium channel subunit alpha-1A	COCON_G00208390	Conger conger (European conger)	1	0
A0A9Q1D428	Peptidase A1 domain-containing protein	COCON_G00192970	Conger conger (European conger)	1	0
A0A9Q1D4D7	Potassium channel subfamily K member	COCON_G00192210	Conger conger (European conger)	1	0
A0A9Q1D4J3	P2X purinoceptor	COCON_G00192000	Conger conger (European conger)	1	0

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