Atlas of Genetics and Cytogenetics in Oncology and Haematology


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ST13P22 (ST13, Hsp70 interacting protein pseudogene 22)

Identity

Other alias-
HGNC (Hugo) ST13P22
LocusID (NCBI) 100874521
Atlas_Id 52664
Location 12q23.2  [Link to chromosome band 12q23]
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


External links

Nomenclature
HGNC (Hugo)ST13P22   38865
Cards
Entrez_Gene (NCBI)ST13P22  100874521  ST13, Hsp70 interacting protein pseudogene 22
Aliases
GeneCards (Weizmann)ST13P22
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  - [Contig_View]  ST13P22 [Vega]
TCGA cBioPortalST13P22
AceView (NCBI)ST13P22
Genatlas (Paris)ST13P22
WikiGenes100874521
SOURCE (Princeton)ST13P22
Genetics Home Reference (NIH)ST13P22
Genomic and cartography
GoldenPath hg38 (UCSC)ST13P22  -  
GoldenPath hg19 (UCSC)ST13P22  -  
EnsemblST13P22 - [CytoView hg19]  ST13P22 - [CytoView hg38]
Mapping of homologs : NCBIST13P22 [Mapview hg19]  ST13P22 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ST13P22
Gene ExpressionST13P22 [ NCBI-GEO ]   ST13P22 [ EBI - ARRAY_EXPRESS ]   ST13P22 [ SEEK ]   ST13P22 [ MEM ]
Gene Expression Viewer (FireBrowse)ST13P22 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100874521
GTEX Portal (Tissue expression)ST13P22
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)ST13P22
DMDM Disease mutations100874521
Blocks (Seattle)ST13P22
Protein Interaction databases
BioGRIDST13P22
STRING (EMBL)ST13P22
ZODIACST13P22
Ontologies - Pathways
Huge Navigator ST13P22 [HugePedia]
snp3D : Map Gene to Disease100874521
BioCentury BCIQST13P22
ClinGenST13P22
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100874521
Clinical trialST13P22
Miscellaneous
canSAR (ICR)ST13P22 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineST13P22
EVEXST13P22
GoPubMedST13P22
iHOPST13P22
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 : Tue Nov 21 14:36:46 CET 2017

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