Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

SERTAD2 (SERTA domain containing 2)

Identity

Alias (NCBI)Sei-2
TRIP-Br2
TRIPBR2
HGNC (Hugo) SERTAD2
HGNC Alias symbTRIP-Br2
KIAA0127
Sei-2
HGNC Alias nametranscriptional regulator interacting with the PHS-bromodomain 2
LocusID (NCBI) 9792
Atlas_Id 51099
Location 2p14  [Link to chromosome band 2p14]
Location_base_pair Starts at 64631621 and ends at 64653913 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)
SEL1L (14q31.1) / SERTAD2 (2p14)SEL1L 14q31.1 / SERTAD2 2p14

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)SERTAD2   30784
Cards
Entrez_Gene (NCBI)SERTAD2    SERTA domain containing 2
AliasesSei-2; TRIP-Br2; TRIPBR2
GeneCards (Weizmann)SERTAD2
Ensembl hg19 (Hinxton)ENSG00000179833 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000179833 [Gene_View]  ENSG00000179833 [Sequence]  chr2:64631621-64653913 [Contig_View]  SERTAD2 [Vega]
ICGC DataPortalENSG00000179833
TCGA cBioPortalSERTAD2
AceView (NCBI)SERTAD2
Genatlas (Paris)SERTAD2
SOURCE (Princeton)SERTAD2
Genetics Home Reference (NIH)SERTAD2
Genomic and cartography
GoldenPath hg38 (UCSC)SERTAD2  -     chr2:64631621-64653913 -  2p14   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SERTAD2  -     2p14   [Description]    (hg19-Feb_2009)
GoldenPathSERTAD2 - 2p14 [CytoView hg19]  SERTAD2 - 2p14 [CytoView hg38]
ImmunoBaseENSG00000179833
Genome Data Viewer NCBISERTAD2 [Mapview hg19]  
OMIM617851   
Gene and transcription
Genbank (Entrez)AK124032 AK311117 BC074788 BC074789 BC101639
RefSeq transcript (Entrez)NM_014755
Consensus coding sequences : CCDS (NCBI)SERTAD2
Gene ExpressionSERTAD2 [ NCBI-GEO ]   SERTAD2 [ EBI - ARRAY_EXPRESS ]   SERTAD2 [ SEEK ]   SERTAD2 [ MEM ]
Gene Expression Viewer (FireBrowse)SERTAD2 [ Firebrowse - Broad ]
GenevisibleExpression of SERTAD2 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)9792
GTEX Portal (Tissue expression)SERTAD2
Human Protein AtlasENSG00000179833-SERTAD2 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ14140   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ14140  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ14140
PhosPhoSitePlusQ14140
Domaine pattern : Prosite (Expaxy)SERTA (PS51053)   
Domains : Interpro (EBI)SERTA_dom   
Domain families : Pfam (Sanger)SERTA (PF06031)   
Domain families : Pfam (NCBI)pfam06031   
Conserved Domain (NCBI)SERTAD2
SuperfamilyQ14140
AlphaFold pdb e-kbQ14140   
Human Protein Atlas [tissue]ENSG00000179833-SERTAD2 [tissue]
HPRD18040
Protein Interaction databases
DIP (DOE-UCLA)Q14140
IntAct (EBI)Q14140
BioGRIDSERTAD2
STRING (EMBL)SERTAD2
ZODIACSERTAD2
Ontologies - Pathways
QuickGOQ14140
Ontology : AmiGOtranscription coactivator activity  protein binding  nucleus  nucleus  nucleoplasm  cytoplasm  cytosol  negative regulation of cell growth  chromatin-mediated maintenance of transcription  transcription regulator activity  
Ontology : EGO-EBItranscription coactivator activity  protein binding  nucleus  nucleus  nucleoplasm  cytoplasm  cytosol  negative regulation of cell growth  chromatin-mediated maintenance of transcription  transcription regulator activity  
NDEx NetworkSERTAD2
Atlas of Cancer Signalling NetworkSERTAD2
Wikipedia pathwaysSERTAD2
Orthology - Evolution
OrthoDB9792
GeneTree (enSembl)ENSG00000179833
Phylogenetic Trees/Animal Genes : TreeFamSERTAD2
Homologs : HomoloGeneSERTAD2
Homology/Alignments : Family Browser (UCSC)SERTAD2
Gene fusions - Rearrangements
Fusion : MitelmanSEL1L/SERTAD2 [14q31.1/2p14]  
Fusion : QuiverSERTAD2
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerSERTAD2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)SERTAD2
dbVarSERTAD2
ClinVarSERTAD2
MonarchSERTAD2
1000_GenomesSERTAD2 
Exome Variant ServerSERTAD2
GNOMAD BrowserENSG00000179833
Varsome BrowserSERTAD2
ACMGSERTAD2 variants
VarityQ14140
Genomic Variants (DGV)SERTAD2 [DGVbeta]
DECIPHERSERTAD2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisSERTAD2 
Mutations
ICGC Data PortalSERTAD2 
TCGA Data PortalSERTAD2 
Broad Tumor PortalSERTAD2
OASIS PortalSERTAD2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICSERTAD2  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DSERTAD2
Mutations and Diseases : HGMDSERTAD2
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaSERTAD2
DgiDB (Drug Gene Interaction Database)SERTAD2
DoCM (Curated mutations)SERTAD2
CIViC (Clinical Interpretations of Variants in Cancer)SERTAD2
Cancer3DSERTAD2
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM617851   
Orphanet
DisGeNETSERTAD2
MedgenSERTAD2
Genetic Testing Registry SERTAD2
NextProtQ14140 [Medical]
GENETestsSERTAD2
Target ValidationSERTAD2
Huge Navigator SERTAD2 [HugePedia]
ClinGenSERTAD2
Clinical trials, drugs, therapy
MyCancerGenomeSERTAD2
Protein Interactions : CTDSERTAD2
Pharm GKB GenePA134948884
PharosQ14140
Clinical trialSERTAD2
Miscellaneous
canSAR (ICR)SERTAD2
HarmonizomeSERTAD2
DataMed IndexSERTAD2
Probes
Litterature
PubMed17 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXSERTAD2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Oct 4 15:30:44 CEST 2021

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.