GlyCosmos Portal

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Displaying entries **12251 - 12275** 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
P0DP24	Calmodulin-2	CALM2 CAM2 CAMB	Homo sapiens (human)	0	1
P0DP25	Calmodulin-3	CALM3 CALML2 CAM3 CAMC CAMIII	Homo sapiens (human)	0	1
O80683	Calmodulin-binding protein 25	CAMBP25 VQ15	Arabidopsis thaliana (thale cress)	0	1
Q9FK63	Calmodulin-binding receptor kinase CaMRLK	CAMRLK MEE62	Arabidopsis thaliana (thale cress)	15	0
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
A2AHC3	Calmodulin-regulated spectrin-associated protein 1	Camsap1	Mus musculus (house mouse)	3	1
Q08AD1	Calmodulin-regulated spectrin-associated protein 2	CAMSAP2 CAMSAP1L1 KIAA1078	Homo sapiens (human)	1	1
Q80VC9	Calmodulin-regulated spectrin-associated protein 3	Camsap3 Kiaa1543	Mus musculus (house mouse)	4	2
Q9P1Y5	Calmodulin-regulated spectrin-associated protein 3	CAMSAP3 KIAA1543	Homo sapiens (human)	5	1
P34652	Calnexin	cnx-1	Caenorhabditis elegans	2	0
P35564	Calnexin	Canx	Mus musculus (house mouse)	2	2
A0A5F9DU78	Calnexin	CANX	Oryctolagus cuniculus (rabbit)	0	1
A8XA40	Calnexin	cnx-1	Caenorhabditis briggsae	1	0
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
Q9I7S9	Calnexin 99A	Dmel\CG1924	Drosophila melanogaster (fruit fly)	0	1
P27825	Calnexin homolog	CNE1	Saccharomyces cerevisiae S288C	5	0
Q6Q487	Calnexin homolog	AFUA_4G12850	Aspergillus fumigatus Af293	1	0
P36581	Calnexin homolog	cal1 cnx1	Schizosaccharomyces pombe 972h-	1	0
P29402	Calnexin homolog 1	CNX1	Arabidopsis thaliana (thale cress)	1	0
Q38798	Calnexin homolog 2	At5g07340	Arabidopsis thaliana (thale cress)	1	0
D4AVD4	Calnexin homolog ARB_00147	ARB_00147	Trichophyton benhamiae CBS 112371	1	0
V5APL8	Calpain catalytic domain-containing protein	TCDM_09599	Trypanosoma cruzi Dm28c	0	1

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