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TCEAL8 (transcription elongation factor A like 8)

Identity

Alias (NCBI)WEX3
HGNC (Hugo) TCEAL8
HGNC Alias symbMGC45400
WEX3
HGNC Previous nametranscription elongation factor A (SII)-like 8
LocusID (NCBI) 90843
Atlas_Id 74568
Location Xq22.1  [Link to chromosome band Xq22]
Location_base_pair Starts at 103252995 and ends at 103255155 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)TCEAL8   28683
Cards
Entrez_Gene (NCBI)TCEAL8    transcription elongation factor A like 8
AliasesWEX3
GeneCards (Weizmann)TCEAL8
Ensembl hg19 (Hinxton)ENSG00000180964 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000180964 [Gene_View]  ENSG00000180964 [Sequence]  chrX:103252995-103255155 [Contig_View]  TCEAL8 [Vega]
ICGC DataPortalENSG00000180964
TCGA cBioPortalTCEAL8
AceView (NCBI)TCEAL8
Genatlas (Paris)TCEAL8
SOURCE (Princeton)TCEAL8
Genetics Home Reference (NIH)TCEAL8
Genomic and cartography
GoldenPath hg38 (UCSC)TCEAL8  -     chrX:103252995-103255155 -  Xq22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TCEAL8  -     Xq22.1   [Description]    (hg19-Feb_2009)
GoldenPathTCEAL8 - Xq22.1 [CytoView hg19]  TCEAL8 - Xq22.1 [CytoView hg38]
ImmunoBaseENSG00000180964
Genome Data Viewer NCBITCEAL8 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK026349 AL833632 BC035573 BU932815
RefSeq transcript (Entrez)NM_001006684 NM_153333
Consensus coding sequences : CCDS (NCBI)TCEAL8
Gene ExpressionTCEAL8 [ NCBI-GEO ]   TCEAL8 [ EBI - ARRAY_EXPRESS ]   TCEAL8 [ SEEK ]   TCEAL8 [ MEM ]
Gene Expression Viewer (FireBrowse)TCEAL8 [ Firebrowse - Broad ]
GenevisibleExpression of TCEAL8 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)90843
GTEX Portal (Tissue expression)TCEAL8
Human Protein AtlasENSG00000180964-TCEAL8 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8IYN2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8IYN2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8IYN2
PhosPhoSitePlusQ8IYN2
Domains : Interpro (EBI)TF_A-like/BEX   
Domain families : Pfam (Sanger)BEX (PF04538)   
Domain families : Pfam (NCBI)pfam04538   
Conserved Domain (NCBI)TCEAL8
SuperfamilyQ8IYN2
AlphaFold pdb e-kbQ8IYN2   
Human Protein Atlas [tissue]ENSG00000180964-TCEAL8 [tissue]
HPRD06656
Protein Interaction databases
DIP (DOE-UCLA)Q8IYN2
IntAct (EBI)Q8IYN2
BioGRIDTCEAL8
STRING (EMBL)TCEAL8
ZODIACTCEAL8
Ontologies - Pathways
QuickGOQ8IYN2
Ontology : AmiGOprotein binding  nucleus  WW domain binding  
Ontology : EGO-EBIprotein binding  nucleus  WW domain binding  
NDEx NetworkTCEAL8
Atlas of Cancer Signalling NetworkTCEAL8
Wikipedia pathwaysTCEAL8
Orthology - Evolution
OrthoDB90843
GeneTree (enSembl)ENSG00000180964
Phylogenetic Trees/Animal Genes : TreeFamTCEAL8
Homologs : HomoloGeneTCEAL8
Homology/Alignments : Family Browser (UCSC)TCEAL8
Gene fusions - Rearrangements
Fusion : QuiverTCEAL8
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTCEAL8 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TCEAL8
dbVarTCEAL8
ClinVarTCEAL8
MonarchTCEAL8
1000_GenomesTCEAL8 
Exome Variant ServerTCEAL8
GNOMAD BrowserENSG00000180964
Varsome BrowserTCEAL8
ACMGTCEAL8 variants
VarityQ8IYN2
Genomic Variants (DGV)TCEAL8 [DGVbeta]
DECIPHERTCEAL8 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTCEAL8 
Mutations
ICGC Data PortalTCEAL8 
TCGA Data PortalTCEAL8 
Broad Tumor PortalTCEAL8
OASIS PortalTCEAL8 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTCEAL8  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTCEAL8
Mutations and Diseases : HGMDTCEAL8
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTCEAL8
DgiDB (Drug Gene Interaction Database)TCEAL8
DoCM (Curated mutations)TCEAL8
CIViC (Clinical Interpretations of Variants in Cancer)TCEAL8
Cancer3DTCEAL8
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTCEAL8
MedgenTCEAL8
Genetic Testing Registry TCEAL8
NextProtQ8IYN2 [Medical]
GENETestsTCEAL8
Target ValidationTCEAL8
Huge Navigator TCEAL8 [HugePedia]
ClinGenTCEAL8
Clinical trials, drugs, therapy
MyCancerGenomeTCEAL8
Protein Interactions : CTDTCEAL8
Pharm GKB GenePA134991274
PharosQ8IYN2
Clinical trialTCEAL8
Miscellaneous
canSAR (ICR)TCEAL8
HarmonizomeTCEAL8
DataMed IndexTCEAL8
Probes
Litterature
PubMed12 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTCEAL8
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Mon Oct 4 16:25:03 CEST 2021

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