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 **2676 - 2700** 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
Q13324	Corticotropin-releasing factor receptor 2	CRHR2 CRF2R CRH2R	Homo sapiens (human)	5	0
P24387	Corticotropin-releasing factor-binding protein	CRHBP CRFBP	Homo sapiens (human)	1	9
P78310	Coxsackievirus and adenovirus receptor	CXADR CAR	Homo sapiens (human)	10	22
Q9UEE9	Craniofacial development protein 1	CFDP1 BCNT CENP-29	Homo sapiens (human)	2	1
P12277	Creatine kinase B-type	CKB CKBB	Homo sapiens (human)	0	1
V9HW77	Creatine kinase B-type	HEL-211	Homo sapiens (human)	0	1
P06732	Creatine kinase M-type	CKM CKMM	Homo sapiens (human)	0	1
P17540	Creatine kinase S-type, mitochondrial	CKMT2	Homo sapiens (human)	0	1
P12532	Creatine kinase U-type, mitochondrial	CKMT1A CKMT1B CKMT	Homo sapiens (human)	1	1
P46109	Crk-like protein	CRKL	Homo sapiens (human)	1	1
Q9BZJ0	Crooked neck-like protein 1	CRNKL1 CRN	Homo sapiens (human)	1	2
P0CG36	Cryptic family protein 1B	CFC1B	Homo sapiens (human)	1	0
P0CG37	Cryptic protein	CFC1	Homo sapiens (human)	1	0	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 B-cell lymphoma Langerhans-cell histiocytosis Marfan syndrome Pick's disease Reye syndrome aromatase excess syndrome arteriosclerotic cardiovascular disease atherosclerosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atrioventricular septal defect autoimmune hepatitis biliary atresia cancer cardiofaciocutaneous syndrome 1 cardiofaciocutaneous syndrome cardiovascular system disease cerebral degeneration congenital adrenal hyperplasia congenital heart disease coronary artery disease dextro-looped transposition of the great arteries disease of metabolism double outlet right ventricle embryoma essential thrombocythemia gallbladder disease gastric adenocarcinoma gastrointestinal system cancer heart disease hepatitis liver disease lymphoma malaria multiple types of congenital heart defects 6 myelodysplastic syndrome neuroblastoma non-Hodgkin lymphoma obsolete dextro-looped transposition of the great arteries 1 obsolete ymphosarcoma patent foramen ovale reticulosarcoma right atrial isomerism schizophrenia situs inversus tuberculosis tuberous sclerosis visceral heterotaxy
O60494	Cubilin	CUBN IFCR	Homo sapiens (human)	54	174
Q13616	Cullin-1	CUL1	Homo sapiens (human)	0	1
Q13617	Cullin-2	CUL2	Homo sapiens (human)	2	3
Q13618	Cullin-3	CUL3 KIAA0617	Homo sapiens (human)	1	2
Q13619	Cullin-4A	CUL4A	Homo sapiens (human)	1	1
Q13620	Cullin-4B	CUL4B KIAA0695	Homo sapiens (human)	10	3
Q93034	Cullin-5	CUL5 VACM1	Homo sapiens (human)	1	2
Q14999	Cullin-7	CUL7 KIAA0076	Homo sapiens (human)	1	2
Q86VP6	Cullin-associated NEDD8-dissociated protein 1	CAND1 KIAA0829 TIP120 TIP120A	Homo sapiens (human)	1	1
O75155	Cullin-associated NEDD8-dissociated protein 2	CAND2 KIAA0667 TIP120B	Homo sapiens (human)	1	2
P18846	Cyclic AMP-dependent transcription factor ATF-1	ATF1	Homo sapiens (human)	16	3
P15336	Cyclic AMP-dependent transcription factor ATF-2	ATF2 CREB2 CREBP1	Homo sapiens (human)	15	2

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