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NOL4L-DT (NOL4L divergent transcript)

Identity

Other alias-
HGNC (Hugo) NOL4L-DT
LocusID (NCBI) 149950
Atlas_Id 80066
Location 20q11.21  [Link to chromosome band 20q11]
Location_base_pair Starts at 32587479 and ends at 32608892 bp from pter ( according to hg38-Dec_2013)
Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute


External links

Nomenclature
HGNC (Hugo)NOL4L-DT   44310
Cards
Entrez_Gene (NCBI)NOL4L-DT  149950  NOL4L divergent transcript
Aliases
GeneCards (Weizmann)NOL4L-DT
Ensembl hg19 (Hinxton)ENSG00000204393 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000204393 [Gene_View]  chr20:32587479-32608892 [Contig_View]  NOL4L-DT [Vega]
ICGC DataPortalENSG00000204393
TCGA cBioPortalNOL4L-DT
AceView (NCBI)NOL4L-DT
Genatlas (Paris)NOL4L-DT
WikiGenes149950
SOURCE (Princeton)NOL4L-DT
Genetics Home Reference (NIH)NOL4L-DT
Genomic and cartography
GoldenPath hg38 (UCSC)NOL4L-DT  -     chr20:32587479-32608892 +  20q11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)NOL4L-DT  -     20q11.21   [Description]    (hg19-Feb_2009)
EnsemblNOL4L-DT - 20q11.21 [CytoView hg19]  NOL4L-DT - 20q11.21 [CytoView hg38]
Mapping of homologs : NCBINOL4L-DT [Mapview hg19]  NOL4L-DT [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC111383 BC130462 BC130464
RefSeq transcript (Entrez)NM_001010976
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)NOL4L-DT
Cluster EST : UnigeneHs.516980 [ NCBI ]
CGAP (NCI)Hs.516980
Alternative Splicing GalleryENSG00000204393
Gene ExpressionNOL4L-DT [ NCBI-GEO ]   NOL4L-DT [ EBI - ARRAY_EXPRESS ]   NOL4L-DT [ SEEK ]   NOL4L-DT [ MEM ]
Gene Expression Viewer (FireBrowse)NOL4L-DT [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)149950
GTEX Portal (Tissue expression)NOL4L-DT
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5W150   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5W150  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5W150
Splice isoforms : SwissVarQ5W150
PhosPhoSitePlusQ5W150
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)NOL4L-DT
DMDM Disease mutations149950
Blocks (Seattle)NOL4L-DT
SuperfamilyQ5W150
Human Protein AtlasENSG00000204393
Peptide AtlasQ5W150
IPIIPI00086068   
Protein Interaction databases
DIP (DOE-UCLA)Q5W150
IntAct (EBI)Q5W150
FunCoupENSG00000204393
BioGRIDNOL4L-DT
STRING (EMBL)NOL4L-DT
ZODIACNOL4L-DT
Ontologies - Pathways
QuickGOQ5W150
Ontology : AmiGOprotein binding  
Ontology : EGO-EBIprotein binding  
NDEx NetworkNOL4L-DT
Atlas of Cancer Signalling NetworkNOL4L-DT
Wikipedia pathwaysNOL4L-DT
Orthology - Evolution
OrthoDB149950
GeneTree (enSembl)ENSG00000204393
Phylogenetic Trees/Animal Genes : TreeFamNOL4L-DT
HOVERGENQ5W150
HOGENOMQ5W150
Homologs : HomoloGeneNOL4L-DT
Homology/Alignments : Family Browser (UCSC)NOL4L-DT
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerNOL4L-DT [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)NOL4L-DT
dbVarNOL4L-DT
ClinVarNOL4L-DT
1000_GenomesNOL4L-DT 
Exome Variant ServerNOL4L-DT
ExAC (Exome Aggregation Consortium)NOL4L-DT (select the gene name)
Genetic variants : HAPMAP149950
Genomic Variants (DGV)NOL4L-DT [DGVbeta]
DECIPHERNOL4L-DT [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisNOL4L-DT 
Mutations
ICGC Data PortalNOL4L-DT 
TCGA Data PortalNOL4L-DT 
Broad Tumor PortalNOL4L-DT
OASIS PortalNOL4L-DT [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDNOL4L-DT
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
BioMutasearch NOL4L-DT
DgiDB (Drug Gene Interaction Database)NOL4L-DT
DoCM (Curated mutations)NOL4L-DT (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)NOL4L-DT (select a term)
intoGenNOL4L-DT
Cancer3DNOL4L-DT(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenNOL4L-DT
Genetic Testing Registry NOL4L-DT
NextProtQ5W150 [Medical]
TSGene149950
GENETestsNOL4L-DT
Target ValidationNOL4L-DT
Huge Navigator NOL4L-DT [HugePedia]
snp3D : Map Gene to Disease149950
BioCentury BCIQNOL4L-DT
ClinGenNOL4L-DT
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD149950
Clinical trialNOL4L-DT
Miscellaneous
canSAR (ICR)NOL4L-DT (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineNOL4L-DT
EVEXNOL4L-DT
GoPubMedNOL4L-DT
iHOPNOL4L-DT
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:32:10 CEST 2017

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