| ATXN1 (6p22.3) / NFE2L1 (17q21.32) | HBA2 (16p13.3) / NFE2L1 (17q21.32) | MICB (6p21.33) / NFE2L1 (17q21.32) |
|
NFE2L1 (17q21.32) / CCDC36 (3p21.31) | NFE2L1 (17q21.32) / EFHD1 (2q37.1) | NFE2L1 (17q21.32) / NFE2L1 (17q21.32) |
|
NFE2L1 (17q21.32) / PRKCSH (19p13.2) | NFE2L1 (17q21.32) / SKAP1 (17q21.32) | NFE2L1 (17q21.32) / SLC39A11 (17q24.3) |
|
NFE2L1 (17q21.32) / TSPAN11 (12p11.21) | NOS1 (12q24.22) / NFE2L1 (17q21.32) | NFE2L1 17q21.32 / SLC39A11 17q24.3 |
|
| Nomenclature |
HGNC (Hugo) | NFE2L1 7781 |
| Cards |
Entrez_Gene (NCBI) | NFE2L1 4779 nuclear factor, erythroid 2 like 1 |
Aliases | LCR-F1; NRF1; TCF11 |
GeneCards (Weizmann) | NFE2L1 |
Ensembl hg19 (Hinxton) | ENSG00000082641 [Gene_View] |
Ensembl hg38 (Hinxton) | ENSG00000082641 [Gene_View]  ENSG00000082641 [Sequence] chr17:48048324-48061545 [Contig_View] NFE2L1 [Vega] |
ICGC DataPortal | ENSG00000082641 |
TCGA cBioPortal | NFE2L1 |
AceView (NCBI) | NFE2L1 |
Genatlas (Paris) | NFE2L1 |
WikiGenes | 4779 |
SOURCE (Princeton) | NFE2L1 |
Genetics Home Reference (NIH) | NFE2L1 |
| Genomic and cartography |
GoldenPath hg38 (UCSC) | NFE2L1 - chr17:48048324-48061545 + 17q21.32 [Description] (hg38-Dec_2013) |
GoldenPath hg19 (UCSC) | NFE2L1 - 17q21.32 [Description] (hg19-Feb_2009) |
GoldenPath | NFE2L1 - 17q21.32 [CytoView hg19] NFE2L1 - 17q21.32 [CytoView hg38] |
ImmunoBase | ENSG00000082641 |
Mapping of homologs : NCBI | NFE2L1 [Mapview hg19] NFE2L1 [Mapview hg38] |
OMIM | 163260 |
| Gene and transcription |
Genbank (Entrez) | AK090459 AK294553 AK302387 AL530578 AL833530 |
RefSeq transcript (Entrez) | NM_001330261 NM_001330262 NM_003204 |
RefSeq genomic (Entrez) | |
Consensus coding sequences : CCDS (NCBI) | NFE2L1 |
Cluster EST : Unigene | Hs.514284 [ NCBI ] |
CGAP (NCI) | Hs.514284 |
Alternative Splicing Gallery | ENSG00000082641 |
Gene Expression | NFE2L1 [ NCBI-GEO ] NFE2L1 [ EBI - ARRAY_EXPRESS ]
NFE2L1 [ SEEK ] NFE2L1 [ MEM ] |
Gene Expression Viewer (FireBrowse) | NFE2L1 [ Firebrowse - Broad ] |
SOURCE (Princeton) | Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60] |
Genevestigator | Expression in : [tissues]  [cell-lines]  [cancer]  [perturbations]   |
BioGPS (Tissue expression) | 4779 |
GTEX Portal (Tissue expression) | NFE2L1 |
Human Protein Atlas | ENSG00000082641-NFE2L1 [pathology] [cell] [tissue] |
| Protein : pattern, domain, 3D structure |
UniProt/SwissProt | Q14494 [function] [subcellular_location] [family_and_domains] [pathology_and_biotech] [ptm_processing] [expression] [interaction] |
NextProt | Q14494 [Sequence] [Exons] [Medical] [Publications] |
With graphics : InterPro | Q14494 |
Splice isoforms : SwissVar | Q14494 |
PhosPhoSitePlus | Q14494 |
Domaine pattern : Prosite (Expaxy) | BZIP (PS50217) BZIP_BASIC (PS00036) |
Domains : Interpro (EBI) | bZIP bZIP_Maf Nrf1_NFE2L1 TF_DNA-bd_sf |
Domain families : Pfam (Sanger) | bZIP_Maf (PF03131) |
Domain families : Pfam (NCBI) | pfam03131 |
Domain families : Smart (EMBL) | BRLZ (SM00338) |
Conserved Domain (NCBI) | NFE2L1 |
DMDM Disease mutations | 4779 |
Blocks (Seattle) | NFE2L1 |
Superfamily | Q14494 |
Human Protein Atlas [tissue] | ENSG00000082641-NFE2L1 [tissue] |
Peptide Atlas | Q14494 |
HPRD | 01223 |
IPI | IPI00031017 IPI00414968 IPI01015922 IPI00376971 |
| Protein Interaction databases |
DIP (DOE-UCLA) | Q14494 |
IntAct (EBI) | Q14494 |
FunCoup | ENSG00000082641 |
BioGRID | NFE2L1 |
STRING (EMBL) | NFE2L1 |
ZODIAC | NFE2L1 |
| Ontologies - Pathways |
QuickGO | Q14494 |
Ontology : AmiGO | protein polyubiquitination transcription regulatory region sequence-specific DNA binding RNA polymerase II distal enhancer sequence-specific DNA binding DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription activator activity, RNA polymerase II-specific DNA-binding transcription factor activity transcription coregulator activity protein binding nucleus nucleus cytoplasm endoplasmic reticulum membrane cytosol fructose 6-phosphate metabolic process transcription by RNA polymerase II glutathione metabolic process heme biosynthetic process inflammatory response regulation of mitotic nuclear division cholesterol metabolic process anatomical structure morphogenesis regulation of glucose metabolic process cholesterol binding integral component of membrane regulation of fatty acid metabolic process cellular homeostasis protein domain specific binding spinal cord motor neuron differentiation glial cell fate commitment erythrocyte differentiation protein-containing complex cellular response to oxidative stress response to endoplasmic reticulum stress cholesterol homeostasis cysteine transport protein-containing complex binding positive regulation of transcription, DNA-templated positive regulation of transcription by RNA polymerase II regulation of inflammatory response glucose 6-phosphate metabolic process regulation of proteasomal protein catabolic process regulation of transcription from RNA polymerase II promoter in response to copper ion cellular response to cold cellular response to cholesterol regulation of nucleus organization regulation of response to endoplasmic reticulum stress promoter-specific chromatin binding |
Ontology : EGO-EBI | protein polyubiquitination transcription regulatory region sequence-specific DNA binding RNA polymerase II distal enhancer sequence-specific DNA binding DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription activator activity, RNA polymerase II-specific DNA-binding transcription factor activity transcription coregulator activity protein binding nucleus nucleus cytoplasm endoplasmic reticulum membrane cytosol fructose 6-phosphate metabolic process transcription by RNA polymerase II glutathione metabolic process heme biosynthetic process inflammatory response regulation of mitotic nuclear division cholesterol metabolic process anatomical structure morphogenesis regulation of glucose metabolic process cholesterol binding integral component of membrane regulation of fatty acid metabolic process cellular homeostasis protein domain specific binding spinal cord motor neuron differentiation glial cell fate commitment erythrocyte differentiation protein-containing complex cellular response to oxidative stress response to endoplasmic reticulum stress cholesterol homeostasis cysteine transport protein-containing complex binding positive regulation of transcription, DNA-templated positive regulation of transcription by RNA polymerase II regulation of inflammatory response glucose 6-phosphate metabolic process regulation of proteasomal protein catabolic process regulation of transcription from RNA polymerase II promoter in response to copper ion cellular response to cold cellular response to cholesterol regulation of nucleus organization regulation of response to endoplasmic reticulum stress promoter-specific chromatin binding |
NDEx Network | NFE2L1 |
Atlas of Cancer Signalling Network | NFE2L1 |
Wikipedia pathways | NFE2L1 |
| Orthology - Evolution |
OrthoDB | 4779 |
GeneTree (enSembl) | ENSG00000082641 |
Phylogenetic Trees/Animal Genes : TreeFam | NFE2L1 |
HOGENOM | Q14494 |
Homologs : HomoloGene | NFE2L1 |
Homology/Alignments : Family Browser (UCSC) | NFE2L1 |
| Gene fusions - Rearrangements |
Fusion : Mitelman | NFE2L1/SLC39A11 [17q21.32/17q24.3]   |
Fusion Portal | NFE2L1 17q21.32 SLC39A11 17q24.3 SKCM |
Fusion : Quiver | NFE2L1 |
| Polymorphisms : SNP and Copy number variants |
NCBI Variation Viewer | NFE2L1 [hg38] |
dbSNP Single Nucleotide Polymorphism (NCBI) | NFE2L1 |
dbVar | NFE2L1 |
ClinVar | NFE2L1 |
1000_Genomes | NFE2L1 |
Exome Variant Server | NFE2L1 |
ExAC (Exome Aggregation Consortium) | ENSG00000082641 |
GNOMAD Browser | ENSG00000082641 |
Varsome Browser | NFE2L1 |
Genetic variants : HAPMAP | 4779 |
Genomic Variants (DGV) | NFE2L1 [DGVbeta] |
DECIPHER | NFE2L1 [patients] [syndromes] [variants] [genes] |
CONAN: Copy Number Analysis | NFE2L1 |
| Mutations |
ICGC Data Portal | NFE2L1 |
TCGA Data Portal | NFE2L1 |
Broad Tumor Portal | NFE2L1 |
OASIS Portal | NFE2L1 [ Somatic mutations - Copy number] |
Somatic Mutations in Cancer : COSMIC | NFE2L1 [overview] [genome browser] [tissue] [distribution] |
Somatic Mutations in Cancer : COSMIC3D | NFE2L1 |
Mutations and Diseases : HGMD | NFE2L1 |
LOVD (Leiden Open Variation Database) | Whole genome datasets |
LOVD (Leiden Open Variation Database) | LOVD - Leiden Open Variation Database |
LOVD (Leiden Open Variation Database) | LOVD 3.0 shared installation |
BioMuta | search NFE2L1 |
DgiDB (Drug Gene Interaction Database) | NFE2L1 |
DoCM (Curated mutations) | NFE2L1 (select the gene name) |
CIViC (Clinical Interpretations of Variants in Cancer) | NFE2L1 (select a term) |
intoGen | NFE2L1 |
Cancer3D | NFE2L1(select the gene name) |
Impact of mutations | [PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser] |
| Diseases |
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OMIM | 163260 |
Orphanet | |
DisGeNET | NFE2L1 |
Medgen | NFE2L1 |
Genetic Testing Registry | NFE2L1
|
NextProt | Q14494 [Medical] |
TSGene | 4779 |
GENETests | NFE2L1 |
Target Validation | NFE2L1 |
Huge Navigator |
NFE2L1 [HugePedia] |
snp3D : Map Gene to Disease | 4779 |
BioCentury BCIQ | NFE2L1 |
ClinGen | NFE2L1 |
| Clinical trials, drugs, therapy |
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Chemical/Protein Interactions : CTD | 4779 |
Chemical/Pharm GKB Gene | PA31587 |
Clinical trial | NFE2L1 |
| Miscellaneous |
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canSAR (ICR) | NFE2L1 (select the gene name) |
DataMed Index | NFE2L1 |
| Probes |
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| Litterature |
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PubMed | 70 Pubmed reference(s) in Entrez |
GeneRIFs | Gene References Into Functions (Entrez) |
CoreMine | NFE2L1 |
EVEX | NFE2L1 |
GoPubMed | NFE2L1 |
iHOP | NFE2L1 |