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ZNF705B (zinc finger protein 705B)

Identity

Other alias-
HGNC (Hugo) ZNF705B
LocusID (NCBI) 100132396
Atlas_Id 76345
Location 8p23.1  [Link to chromosome band 8p23]
Location_base_pair Starts at 7926337 and ends at 7952413 bp from pter ( according to hg38-Dec_2013)

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)ZNF705B   32284
Cards
Entrez_Gene (NCBI)ZNF705B  100132396  zinc finger protein 705B
Aliases
GeneCards (Weizmann)ZNF705B
Ensembl hg19 (Hinxton)ENSG00000215356 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000215356 [Gene_View]  chr8:7926337-7952413 [Contig_View]  ZNF705B [Vega]
ICGC DataPortalENSG00000215356
TCGA cBioPortalZNF705B
AceView (NCBI)ZNF705B
Genatlas (Paris)ZNF705B
WikiGenes100132396
SOURCE (Princeton)ZNF705B
Genetics Home Reference (NIH)ZNF705B
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF705B  -     chr8:7926337-7952413 +  8p23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF705B  -     8p23.1   [Description]    (hg19-Feb_2009)
EnsemblZNF705B - 8p23.1 [CytoView hg19]  ZNF705B - 8p23.1 [CytoView hg38]
Mapping of homologs : NCBIZNF705B [Mapview hg19]  ZNF705B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK292586
RefSeq transcript (Entrez)NM_001193630
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF705B
Cluster EST : UnigeneHs.546691 [ NCBI ]
CGAP (NCI)Hs.546691
Alternative Splicing GalleryENSG00000215356
Gene ExpressionZNF705B [ NCBI-GEO ]   ZNF705B [ EBI - ARRAY_EXPRESS ]   ZNF705B [ SEEK ]   ZNF705B [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF705B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100132396
GTEX Portal (Tissue expression)ZNF705B
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0CI00   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0CI00  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0CI00
Splice isoforms : SwissVarP0CI00
PhosPhoSitePlusP0CI00
Domaine pattern : Prosite (Expaxy)KRAB (PS50805)    ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)KRAB    Znf_C2H2    Znf_C2H2-like    Znf_C2H2/integrase_DNA-bd   
Domain families : Pfam (Sanger)KRAB (PF01352)    zf-C2H2 (PF00096)   
Domain families : Pfam (NCBI)pfam01352    pfam00096   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF705B
DMDM Disease mutations100132396
Blocks (Seattle)ZNF705B
SuperfamilyP0CI00
Human Protein AtlasENSG00000215356
Peptide AtlasP0CI00
IPIIPI00954076   IPI00455832   
Protein Interaction databases
DIP (DOE-UCLA)P0CI00
IntAct (EBI)P0CI00
FunCoupENSG00000215356
BioGRIDZNF705B
STRING (EMBL)ZNF705B
ZODIACZNF705B
Ontologies - Pathways
QuickGOP0CI00
Ontology : AmiGODNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
Ontology : EGO-EBIDNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
NDEx NetworkZNF705B
Atlas of Cancer Signalling NetworkZNF705B
Wikipedia pathwaysZNF705B
Orthology - Evolution
OrthoDB100132396
GeneTree (enSembl)ENSG00000215356
Phylogenetic Trees/Animal Genes : TreeFamZNF705B
HOVERGENP0CI00
HOGENOMP0CI00
Homologs : HomoloGeneZNF705B
Homology/Alignments : Family Browser (UCSC)ZNF705B
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF705B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF705B
dbVarZNF705B
ClinVarZNF705B
1000_GenomesZNF705B 
Exome Variant ServerZNF705B
ExAC (Exome Aggregation Consortium)ZNF705B (select the gene name)
Genetic variants : HAPMAP100132396
Genomic Variants (DGV)ZNF705B [DGVbeta]
DECIPHERZNF705B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF705B 
Mutations
ICGC Data PortalZNF705B 
TCGA Data PortalZNF705B 
Broad Tumor PortalZNF705B
OASIS PortalZNF705B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF705B  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF705B
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ZNF705B
DgiDB (Drug Gene Interaction Database)ZNF705B
DoCM (Curated mutations)ZNF705B (select thE genu ame)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF705B (select a term)
intoGenZNF705B
Cancer3DZNF705B(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF705B
Genetic Testing Registry ZNF705B
NextProtP0CI00 [Medical]
TSGene100132396
GENETestsZNF705B
Target ValidationZNF705B
Huge Navigator ZNF705B [HugePedia]
snp3D : Map Gene to Disease100132396
BioCentury BCIQZNF705B
ClinGenZNF705B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100132396
Chemical/Pharm GKB GenePA142670503
Clinical trialZNF705B
Miscellaneous
canSAR (ICR)ZNF705B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF705B
EVEXZNF705B
GoPubMedZNF705B
iHOPZNF705B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:45:12 CEST 2017

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