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TSACC (TSSK6 activating cochaperone)

Identity

Alias (NCBI)C1orf182
SIP
SSTK-IP
HGNC (Hugo) TSACC
HGNC Alias symbSSTK-IP
SIP
HGNC Alias nameSSTK-interacting protein
HGNC Previous nameC1orf182
HGNC Previous namechromosome 1 open reading frame 182
LocusID (NCBI) 128229
Atlas_Id 75218
Location 1q22  [Link to chromosome band 1q22]
Location_base_pair Starts at 156337314 and ends at 156346994 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)TSACC   30636
Cards
Entrez_Gene (NCBI)TSACC    TSSK6 activating cochaperone
AliasesC1orf182; SIP; SSTK-IP
GeneCards (Weizmann)TSACC
Ensembl hg19 (Hinxton)ENSG00000163467 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000163467 [Gene_View]  ENSG00000163467 [Sequence]  chr1:156337314-156346994 [Contig_View]  TSACC [Vega]
ICGC DataPortalENSG00000163467
TCGA cBioPortalTSACC
AceView (NCBI)TSACC
Genatlas (Paris)TSACC
SOURCE (Princeton)TSACC
Genetics Home Reference (NIH)TSACC
Genomic and cartography
GoldenPath hg38 (UCSC)TSACC  -     chr1:156337314-156346994 +  1q22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TSACC  -     1q22   [Description]    (hg19-Feb_2009)
GoldenPathTSACC - 1q22 [CytoView hg19]  TSACC - 1q22 [CytoView hg38]
ImmunoBaseENSG00000163467
Genome Data Viewer NCBITSACC [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AI336861 AK311950 AY048672 AY048673 BC014605
RefSeq transcript (Entrez)NM_001304817 NM_001304818 NM_001304819 NM_001304820 NM_001304821 NM_001304822 NM_001304823 NM_001304824 NM_001304825 NM_001304826 NM_144627
Consensus coding sequences : CCDS (NCBI)TSACC
Gene ExpressionTSACC [ NCBI-GEO ]   TSACC [ EBI - ARRAY_EXPRESS ]   TSACC [ SEEK ]   TSACC [ MEM ]
Gene Expression Viewer (FireBrowse)TSACC [ Firebrowse - Broad ]
GenevisibleExpression of TSACC in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)128229
GTEX Portal (Tissue expression)TSACC
Human Protein AtlasENSG00000163467-TSACC [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96A04   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96A04  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96A04
PhosPhoSitePlusQ96A04
Domains : Interpro (EBI)SSTK-IP   
Domain families : Pfam (Sanger)SSTK-IP (PF15836)   
Domain families : Pfam (NCBI)pfam15836   
Conserved Domain (NCBI)TSACC
SuperfamilyQ96A04
AlphaFold pdb e-kbQ96A04   
Human Protein Atlas [tissue]ENSG00000163467-TSACC [tissue]
HPRD10252
Protein Interaction databases
DIP (DOE-UCLA)Q96A04
IntAct (EBI)Q96A04
BioGRIDTSACC
STRING (EMBL)TSACC
ZODIACTSACC
Ontologies - Pathways
QuickGOQ96A04
Ontology : AmiGOprotein binding  cytoplasm  chaperone binding  chaperone binding  
Ontology : EGO-EBIprotein binding  cytoplasm  chaperone binding  chaperone binding  
NDEx NetworkTSACC
Atlas of Cancer Signalling NetworkTSACC
Wikipedia pathwaysTSACC
Orthology - Evolution
OrthoDB128229
GeneTree (enSembl)ENSG00000163467
Phylogenetic Trees/Animal Genes : TreeFamTSACC
Homologs : HomoloGeneTSACC
Homology/Alignments : Family Browser (UCSC)TSACC
Gene fusions - Rearrangements
Fusion : QuiverTSACC
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTSACC [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TSACC
dbVarTSACC
ClinVarTSACC
MonarchTSACC
1000_GenomesTSACC 
Exome Variant ServerTSACC
GNOMAD BrowserENSG00000163467
Varsome BrowserTSACC
ACMGTSACC variants
VarityQ96A04
Genomic Variants (DGV)TSACC [DGVbeta]
DECIPHERTSACC [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTSACC 
Mutations
ICGC Data PortalTSACC 
TCGA Data PortalTSACC 
Broad Tumor PortalTSACC
OASIS PortalTSACC [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTSACC  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTSACC
Mutations and Diseases : HGMDTSACC
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTSACC
DgiDB (Drug Gene Interaction Database)TSACC
DoCM (Curated mutations)TSACC
CIViC (Clinical Interpretations of Variants in Cancer)TSACC
Cancer3DTSACC
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTSACC
MedgenTSACC
Genetic Testing Registry TSACC
NextProtQ96A04 [Medical]
GENETestsTSACC
Target ValidationTSACC
Huge Navigator TSACC [HugePedia]
ClinGenTSACC
Clinical trials, drugs, therapy
MyCancerGenomeTSACC
Protein Interactions : CTDTSACC
Pharm GKB GenePA142672430
PharosQ96A04
Clinical trialTSACC
Miscellaneous
canSAR (ICR)TSACC
HarmonizomeTSACC
DataMed IndexTSACC
Probes
Litterature
PubMed12 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTSACC
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 16:27:06 CEST 2021

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