ConVarT

ClinVar Data

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Variation ID	Allele ID	RS Number	Variant Type	Record	Alteration	Clinicial Sig.	Last Update	Phenotypes	Cytogenetic	Review Status	RCV Acc.N.

gnomAD

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Variant ID	Transcript ID	Alteration	Annotation	Allele C.	Allele N.	Allele F.	rsNumber	Flags	Filter
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Post-translational Modifications (PTMs)

Acetylation

Methylation

Phosphorylation

Sumoylation

Ubiquitination

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Gene Name	ACC ID	PTM Type	Position	Mod-rsd	Site +/-7 Aa	Mw_kd	Site grpID
ENO1	P06733	Phosphorylation	100	T100-p	LMIEMDGtENkSkFG	47.17	18009344
ENO1	P06733	Ubiquitination	103	K103-ub	EMDGtENkSkFGANA	47.17	21173972
ENO1	P06733	Acetylation	103	K103-ac	EMDGtENkSkFGANA	47.17	14146803
ENO1	P06733	Ubiquitination	105	K105-ub	DGtENkSkFGANAIL	47.17	15388080
ENO1	P06733	Acetylation	105	K105-ac	DGtENkSkFGANAIL	47.17	14146804
ENO1	P06733	Phosphorylation	115	S115-p	ANAILGVsLAVCkAG	47.17	55578724
ENO1	P06733	Ubiquitination	120	K120-ub	GVsLAVCkAGAVEkG	47.17	4332950
ENO1	P06733	Ubiquitination	126	K126-ub	CkAGAVEkGVPLyRH	47.17	10998367
ENO1	P06733	Acetylation	126	K126-ac	CkAGAVEkGVPLyRH	47.17	11321348
ENO1	P06733	Phosphorylation	131	Y131-p	VEkGVPLyRHIADLA	47.17	480720
ENO1	P06733	Phosphorylation	14	S14-p	HArEIFDsrGNPtVE	47.17	13830716
ENO1	P06733	Phosphorylation	141	S141-p	IADLAGNsEVILPVP	47.17	27448189
ENO1	P06733	Methylation	15	R15-m1	ArEIFDsrGNPtVEV	47.17	57737143
ENO1	P06733	Phosphorylation	157	S157-p	FNVINGGsHAGNKLA	47.17	40510555
ENO1	P06733	Methylation	183	R183-m1	ANFREAMrIGAEVyH	47.17	57737138
ENO1	P06733	Phosphorylation	189	Y189-p	MrIGAEVyHNLkNVI	47.17	461956
ENO1	P06733	Phosphorylation	19	T19-p	FDsrGNPtVEVDLFt	47.17	31886658
ENO1	P06733	Ubiquitination	193	K193-ub	AEVyHNLkNVIkEkY	47.17	12304975
ENO1	P06733	Acetylation	193	K193-ac	AEVyHNLkNVIkEkY	47.17	461587
ENO1	P06733	Ubiquitination	197	K197-ub	HNLkNVIkEkYGkDA	47.17	10997835

Showing 1 to 20 of 122 entries

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Catalogue of Somatic Mutations in Cancer (COSMIC)

Gene Name	Transcript ID	Sample name	Primary Site	Primary Histology	Mutation ID	Mutation CDS	Mutation Aa	Mutation Desc.	FATHMM Prediction	FATHMM Score	Mutation Somatic Status	PUBMED PMID	Tumor Origin	Position

dbSNP

Gene ID	Transcript ID	Consequence	Position	HGVSp	Impact

Protein Domains (PFAM)

Pfam Domain	Domain Name	Description	Positions	Clan	Clan Name	Organism
NO RESULT FOUND
PF00113	Enolase_C	Enolase, C-terminal TIM barrel domain	142-432	CL0256	Enolase_TIM	Homo sapiens
PF03952	Enolase_N	Enolase, N-terminal domain	3-134	CL0227	Enolase_N	Homo sapiens

List of the diseases from DisGeNET

Disease Name	Disease Category	DSI*	DPI**
Adenocarcinoma	Neoplasms ;	0.516	0.828
Osteoporosis, Age-Related	Musculoskeletal Diseases ; Nutritional and Metabolic Diseases ;	0.516	0.828
Alzheimer's Disease	Nervous System Diseases ; Mental Disorders ;	0.516	0.828
Rheumatoid Arthritis	Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ;	0.516	0.828
Malignant neoplasm of breast	Neoplasms ; Skin and Connective Tissue Diseases ;	0.516	0.828
Carcinoma	Neoplasms ;	0.516	0.828
Non-Small Cell Lung Carcinoma	Neoplasms ; Respiratory Tract Diseases ;	0.516	0.828
Squamous cell carcinoma	Neoplasms ;	0.516	0.828
Cytopenia	N/A	0.516	0.828
Presenile dementia	Nervous System Diseases ; Mental Disorders ;	0.516	0.828
Esophageal Neoplasms	Neoplasms ; Digestive System Diseases ;	0.516	0.828
Hepatitis, Toxic	Digestive System Diseases ; Chemically-Induced Disorders ;	0.516	0.828
Male infertility	Male Urogenital Diseases ;	0.516	0.828
Malignant neoplasm of stomach	Neoplasms ; Digestive System Diseases ;	0.516	0.828
Animal Mammary Neoplasms	Neoplasms ; Animal Diseases ;	0.516	0.828
Mammary Neoplasms, Experimental	Neoplasms ;	0.516	0.828
Mouth Neoplasms	Neoplasms ; Stomatognathic Diseases ;	0.516	0.828
Neoplasm Invasiveness	Neoplasms ; Pathological Conditions, Signs and Symptoms ;	0.516	0.828
Degenerative polyarthritis	Musculoskeletal Diseases ;	0.516	0.828
Osteoporosis	Musculoskeletal Diseases ; Nutritional and Metabolic Diseases ;	0.516	0.828
Osteoporosis, Senile	Musculoskeletal Diseases ; Nutritional and Metabolic Diseases ;	0.516	0.828
Stomach Neoplasms	Neoplasms ; Digestive System Diseases ;	0.516	0.828
Osteoarthrosis Deformans	Musculoskeletal Diseases ;	0.516	0.828
Adenocarcinoma of lung (disorder)	Neoplasms ; Respiratory Tract Diseases ;	0.516	0.828
Malignant neoplasm of mouth	Neoplasms ; Stomatognathic Diseases ;	0.516	0.828
Congenital anemia	N/A	0.516	0.828
Adenocarcinoma, Basal Cell	Neoplasms ;	0.516	0.828
Adenocarcinoma, Oxyphilic	Neoplasms ;	0.516	0.828
Carcinoma, Cribriform	Neoplasms ;	0.516	0.828
Carcinoma, Granular Cell	Neoplasms ;	0.516	0.828
Adenocarcinoma, Tubular	Neoplasms ;	0.516	0.828
Anaplastic carcinoma	Neoplasms ;	0.516	0.828
Carcinoma, Spindle-Cell	Neoplasms ;	0.516	0.828
Undifferentiated carcinoma	Neoplasms ;	0.516	0.828
Carcinomatosis	Neoplasms ;	0.516	0.828
Familial Alzheimer Disease (FAD)	Nervous System Diseases ; Mental Disorders ;	0.516	0.828
Alzheimer Disease, Late Onset	Nervous System Diseases ; Mental Disorders ;	0.516	0.828
Necrotizing Enterocolitis	Digestive System Diseases ;	0.516	0.828
Acute Confusional Senile Dementia	Nervous System Diseases ; Mental Disorders ;	0.516	0.828
Malignant neoplasm of esophagus	Neoplasms ; Digestive System Diseases ;	0.516	0.828
Breast Carcinoma	Neoplasms ; Skin and Connective Tissue Diseases ;	0.516	0.828
Alzheimer's Disease, Focal Onset	Nervous System Diseases ; Mental Disorders ;	0.516	0.828
Alzheimer Disease, Early Onset	Nervous System Diseases ; Mental Disorders ;	0.516	0.828
Post-Traumatic Osteoporosis	Musculoskeletal Diseases ; Nutritional and Metabolic Diseases ;	0.516	0.828
Subfertility, Male	Male Urogenital Diseases ;	0.516	0.828
Drug-Induced Liver Disease	Digestive System Diseases ; Chemically-Induced Disorders ;	0.516	0.828
Male sterility	Male Urogenital Diseases ;	0.516	0.828
Acute Coronary Syndrome	Cardiovascular Diseases ;	0.516	0.828
Mammary Carcinoma, Animal	Neoplasms ; Animal Diseases ;	0.516	0.828
Mammary Neoplasms, Human	Neoplasms ; Skin and Connective Tissue Diseases ;	0.516	0.828
Hepatitis, Drug-Induced	Digestive System Diseases ; Chemically-Induced Disorders ;	0.516	0.828
Mammary Neoplasms	Neoplasms ; Skin and Connective Tissue Diseases ;	0.516	0.828
Hereditary Diffuse Gastric Cancer	Neoplasms ; Digestive System Diseases ;	0.516	0.828
Liver carcinoma	Neoplasms ; Digestive System Diseases ;	0.516	0.828
Drug-Induced Acute Liver Injury	Digestive System Diseases ; Chemically-Induced Disorders ;	0.516	0.828
Chemical and Drug Induced Liver Injury	Digestive System Diseases ; Chemically-Induced Disorders ;	0.516	0.828
Chemically-Induced Liver Toxicity	Digestive System Diseases ; Chemically-Induced Disorders ;	0.516	0.828
NO RESULT FOUND

Description:	Enolase [Source:FlyBase;Acc:FBgn0000579]
Synonyms:	Eno2, Dmel\CG17654, anon-WO0153538.76, T18, eno, CG17654, ENOA, Dmel_CG17654, BEST:LD15491, T32526
Other ID(s):	FBgn0000579
Protein Accession Numbers:	NP_722722, NP_001162853, NP_722724, NP_722721, NP_722723, NP_477421
Statistics:	ClinVar(2) PTM(122)

Classification of Clinicial Significance of ClinVar Data