GlyCosmos Portal

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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 **1776 - 1800** 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
Q16566	Calcium/calmodulin-dependent protein kinase type IV	CAMK4 CAMK CAMK-GR CAMKIV	Homo sapiens (human)	7	1
Q9HB71	Calcyclin-binding protein	CACYBP S100A6BP SIP	Homo sapiens (human)	1	1
Q13938	Calcyphosin	CAPS	Homo sapiens (human)	2	1
Q05682	Caldesmon	CALD1 CAD CDM	Homo sapiens (human)	5	1
O14967	Calmegin	CLGN	Homo sapiens (human)	1	2	breast cancer breast carcinoma prostate cancer prostate carcinoma seminoma testicular cancer testicular germ cell cancer testis seminoma
Q96JQ2	Calmin	CLMN KIAA1188	Homo sapiens (human)	0	1
P0DP23	Calmodulin-1	CALM1 CALM CAM CAM1	Homo sapiens (human)	0	1
P0DP24	Calmodulin-2	CALM2 CAM2 CAMB	Homo sapiens (human)	0	1
P0DP25	Calmodulin-3	CALM3 CALML2 CAM3 CAMC CAMIII	Homo sapiens (human)	0	1
Q9Y6Y1	Calmodulin-binding transcription activator 1	CAMTA1 KIAA0833	Homo sapiens (human)	1	0
Q9NZT1	Calmodulin-like protein 5	CALML5 CLSP	Homo sapiens (human)	1	2
Q7Z624	Calmodulin-lysine N-methyltransferase	CAMKMT C2orf34 CLNMT	Homo sapiens (human)	1	1
Q5T5Y3	Calmodulin-regulated spectrin-associated protein 1	CAMSAP1	Homo sapiens (human)	4	2
Q08AD1	Calmodulin-regulated spectrin-associated protein 2	CAMSAP2 CAMSAP1L1 KIAA1078	Homo sapiens (human)	1	1
Q9P1Y5	Calmodulin-regulated spectrin-associated protein 3	CAMSAP3 KIAA1543	Homo sapiens (human)	5	1
P27824	Calnexin	CANX	Homo sapiens (human)	11	5	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Lyme disease MASA syndrome Marfan syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 absence epilepsy acute myocardial infarction adult medulloblastoma agenesis of the corpus callosum with peripheral neuropathy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system lymphoma cervical squamous cell carcinoma cervix uteri carcinoma in situ childhood absence epilepsy childhood medulloblastoma childhood osteosarcoma cone-rod dystrophy coronary artery disease coronary thrombosis diabetes mellitus diabetic angiopathy diabetic ketoacidosis embryoma exanthema subitum fundus albipunctatus giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperinsulinism interstitial lung disease keratosis follicularis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma mongolian spot monoclonal gammopathy of uncertain significance motor peripheral neuropathy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple myeloma multiple sclerosis myocardial infarction nephrogenic diabetes insipidus neuropathy nodular prostate obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum oculocutaneous albinism type IA oculocutaneous albinism osteosarcoma peripheral nervous system disease platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 polyneuropathy post-traumatic stress disorder progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pseudoachondroplasia pseudoxanthoma elasticum renal tubular acidosis retinitis pigmentosa rubella silent myocardial infarction situs inversus skin melanoma spinal muscular atrophy stomach cancer stomach carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus vitiligo von Willebrand's disease
P04632	Calpain small subunit 1	CAPNS1 CAPN4 CAPNS	Homo sapiens (human)	4	2
P07384	Calpain-1 catalytic subunit	CAPN1 CANPL1	Homo sapiens (human)	1	2
Q9HC96	Calpain-10	CAPN10 KIAA1845	Homo sapiens (human)	1	1
Q9UMQ6	Calpain-11	CAPN11	Homo sapiens (human)	0	1
O75808	Calpain-15	CAPN15 SOLH	Homo sapiens (human)	0	1
P17655	Calpain-2 catalytic subunit	CAPN2 CANPL2	Homo sapiens (human)	0	1
P20807	Calpain-3	CAPN3 CANP3 CANPL3 NCL1	Homo sapiens (human)	1	2
Q9Y6W3	Calpain-7	CAPN7 PALBH	Homo sapiens (human)	1	1
A6NHC0	Calpain-8	CAPN8 NCL2	Homo sapiens (human)	0	1

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