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TP53TG3E (TP53 target 3 family member E)

Identity

Alias (NCBI)TP53TG3
TP53TG3B
TP53TG3C
TP53TG3D
TP53TG3F
HGNC (Hugo) TP53TG3E
LocusID (NCBI) 102724101
Atlas_Id 78718
Location 16p11.2  [Link to chromosome band 16p11]
Location_base_pair Starts at 32673524 and ends at 32676110 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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

DNA/RNA

 



External links

 

Nomenclature
HGNC (Hugo)TP53TG3E   51816
Cards
Entrez_Gene (NCBI)TP53TG3E    TP53 target 3 family member E
AliasesTP53TG3; TP53TG3B; TP53TG3C; TP53TG3D; 
TP53TG3F
GeneCards (Weizmann)TP53TG3E
Ensembl hg19 (Hinxton)ENSG00000275034 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000275034 [Gene_View]  ENSG00000275034 [Sequence]  chr16:32673524-32676110 [Contig_View]  TP53TG3E [Vega]
ICGC DataPortalENSG00000275034
TCGA cBioPortalTP53TG3E
AceView (NCBI)TP53TG3E
Genatlas (Paris)TP53TG3E
SOURCE (Princeton)TP53TG3E
Genetics Home Reference (NIH)TP53TG3E
Genomic and cartography
GoldenPath hg38 (UCSC)TP53TG3E  -     chr16:32673524-32676110 -  16p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TP53TG3E  -     16p11.2   [Description]    (hg19-Feb_2009)
GoldenPathTP53TG3E - 16p11.2 [CytoView hg19]  TP53TG3E - 16p11.2 [CytoView hg38]
ImmunoBaseENSG00000275034
Genome Data Viewer NCBITP53TG3E [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AB023508 AK097435 AK312220 AL133588 BC096733
RefSeq transcript (Entrez)NM_001330061
Consensus coding sequences : CCDS (NCBI)TP53TG3E
Gene ExpressionTP53TG3E [ NCBI-GEO ]   TP53TG3E [ EBI - ARRAY_EXPRESS ]   TP53TG3E [ SEEK ]   TP53TG3E [ MEM ]
Gene Expression Viewer (FireBrowse)TP53TG3E [ Firebrowse - Broad ]
GenevisibleExpression of TP53TG3E in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)102724101
GTEX Portal (Tissue expression)TP53TG3E
Human Protein AtlasENSG00000275034-TP53TG3E [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9ULZ0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9ULZ0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9ULZ0
PhosPhoSitePlusQ9ULZ0
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TP53TG3E
SuperfamilyQ9ULZ0
AlphaFold pdb e-kbQ9ULZ0   
Human Protein Atlas [tissue]ENSG00000275034-TP53TG3E [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q9ULZ0
IntAct (EBI)Q9ULZ0
BioGRIDTP53TG3E
STRING (EMBL)TP53TG3E
ZODIACTP53TG3E
Ontologies - Pathways
QuickGOQ9ULZ0
Ontology : AmiGOnucleus  cytoplasm  
Ontology : EGO-EBInucleus  cytoplasm  
NDEx NetworkTP53TG3E
Atlas of Cancer Signalling NetworkTP53TG3E
Wikipedia pathwaysTP53TG3E
Orthology - Evolution
OrthoDB102724101
GeneTree (enSembl)ENSG00000275034
Phylogenetic Trees/Animal Genes : TreeFamTP53TG3E
Homologs : HomoloGeneTP53TG3E
Homology/Alignments : Family Browser (UCSC)TP53TG3E
Gene fusions - Rearrangements
Fusion : QuiverTP53TG3E
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTP53TG3E [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TP53TG3E
dbVarTP53TG3E
ClinVarTP53TG3E
MonarchTP53TG3E
1000_GenomesTP53TG3E 
Exome Variant ServerTP53TG3E
GNOMAD BrowserENSG00000275034
Varsome BrowserTP53TG3E
ACMGTP53TG3E variants
VarityQ9ULZ0
Genomic Variants (DGV)TP53TG3E [DGVbeta]
DECIPHERTP53TG3E [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTP53TG3E 
Mutations
ICGC Data PortalTP53TG3E 
TCGA Data PortalTP53TG3E 
Broad Tumor PortalTP53TG3E
OASIS PortalTP53TG3E [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDTP53TG3E
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTP53TG3E
DgiDB (Drug Gene Interaction Database)TP53TG3E
DoCM (Curated mutations)TP53TG3E
CIViC (Clinical Interpretations of Variants in Cancer)TP53TG3E
Cancer3DTP53TG3E
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTP53TG3E
MedgenTP53TG3E
Genetic Testing Registry TP53TG3E
NextProtQ9ULZ0 [Medical]
GENETestsTP53TG3E
Target ValidationTP53TG3E
Huge Navigator TP53TG3E [HugePedia]
ClinGenTP53TG3E
Clinical trials, drugs, therapy
MyCancerGenomeTP53TG3E
Protein Interactions : CTDTP53TG3E
PharosQ9ULZ0
Clinical trialTP53TG3E
Miscellaneous
canSAR (ICR)TP53TG3E
HarmonizomeTP53TG3E
DataMed IndexTP53TG3E
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTP53TG3E
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 16:26:35 CEST 2021

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