ENO2 (GeneID: 2026) | Homo sapiens
Description: enolase 2 [Source:HGNC Symbol;Acc:HGNC:3353]
Synonyms: HEL-S-279, NSE
Other ID(s): HGNC:3353, ENSG00000111674
Protein Accession Numbers: ENST00000535366, ENST00000593874, NP_001966, ENST00000544774, ENST00000597321, ENST00000538763, ENST00000595469, ENST00000535275, ENST00000593797, ENST00000601485, ENST00000543975, ENST00000596533, ENST00000537688, ENST00000594987, ENST00000229277, ENST00000545045, ENST00000600792, ENST00000541477, ENST00000596089
Statistics: gnomAD(77)
gnomAD Variants By Annotation

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000229277 ENST00000535275 ENST00000535366 ENST00000537688 ENST00000538763 ENST00000541477 ENST00000543975 ENST00000544774 ENST00000545045 ENST00000593797 ENST00000593874 ENST00000594987 ENST00000595469 ENST00000596089 ENST00000596533 ENST00000597321 ENST00000600792 ENST00000601485 NP_001966


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

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00113 Enolase_C Enolase, C-terminal TIM barrel domain 95-313 CL0256 Enolase_TIM Mus musculus
PF03952 Enolase_N Enolase, N-terminal domain 3-108 CL0227 Enolase_N Mus musculus

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Malignant neoplasm of urinary bladder Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.559 0.724
Bladder Neoplasm Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.559 0.724
Non-Small Cell Lung Carcinoma Neoplasms ; Respiratory Tract Diseases ; 0.559 0.724
Neoplastic Cell Transformation Neoplasms ; Pathological Conditions, Signs and Symptoms ; 0.559 0.724
Hepatoma, Morris Neoplasms ; Digestive System Diseases ; 0.559 0.724
Hepatoma, Novikoff Neoplasms ; Digestive System Diseases ; 0.559 0.724
Leukemia, Myelocytic, Acute Neoplasms ; 0.559 0.724
Liver Neoplasms, Experimental Neoplasms ; Digestive System Diseases ; 0.559 0.724
Acute Myeloid Leukemia, M1 Neoplasms ; 0.559 0.724
Neoplasms, Experimental Neoplasms ; 0.559 0.724
Schizophrenia Mental Disorders ; 0.559 0.724
Experimental Hepatoma Neoplasms ; Digestive System Diseases ; 0.559 0.724
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.559 0.724
NO RESULT FOUND
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