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ZNF705E (zinc finger protein 705E)

Identity

Other alias-
HGNC (Hugo) ZNF705E
LocusID (NCBI) 100131539
Atlas_Id 76347
Location 11q13.4  [Link to chromosome band 11q13]
Location_base_pair Starts at 71525091 and ends at 71532593 bp from pter ( according to hg19-Feb_2009)

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)ZNF705E   33203
Cards
Entrez_Gene (NCBI)ZNF705E  100131539  zinc finger protein 705E
Aliases
GeneCards (Weizmann)ZNF705E
Ensembl hg19 (Hinxton) [Gene_View]  chr11:71525091-71532593 [Contig_View]  ZNF705E [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr11:71525091-71532593 [Contig_View]  ZNF705E [Vega]
TCGA cBioPortalZNF705E
AceView (NCBI)ZNF705E
Genatlas (Paris)ZNF705E
WikiGenes100131539
SOURCE (Princeton)ZNF705E
Genetics Home Reference (NIH)ZNF705E
Genomic and cartography
GoldenPath hg19 (UCSC)ZNF705E  -     chr11:71525091-71532593 -  11q13.4   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ZNF705E  -     11q13.4   [Description]    (hg38-Dec_2013)
EnsemblZNF705E - 11q13.4 [CytoView hg19]  ZNF705E - 11q13.4 [CytoView hg38]
Mapping of homologs : NCBIZNF705E [Mapview hg19]  ZNF705E [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001278713
RefSeq genomic (Entrez)NC_000011 NC_018922 NT_167190 NW_004929380
Consensus coding sequences : CCDS (NCBI)ZNF705E
Gene ExpressionZNF705E [ NCBI-GEO ]   ZNF705E [ EBI - ARRAY_EXPRESS ]   ZNF705E [ SEEK ]   ZNF705E [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF705E [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100131539
GTEX Portal (Tissue expression)ZNF705E
Protein : pattern, domain, 3D structure
UniProt/SwissProtA8MWA4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA8MWA4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA8MWA4
Splice isoforms : SwissVarA8MWA4
PhosPhoSitePlusA8MWA4
Domaine pattern : Prosite (Expaxy)KRAB (PS50805)    ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)Krueppel-associated_box    Znf_C2H2    Znf_C2H2-like    Znf_C2H2/integrase_DNA-bd   
Domain families : Pfam (Sanger)KRAB (PF01352)   
Domain families : Pfam (NCBI)pfam01352   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF705E
DMDM Disease mutations100131539
Blocks (Seattle)ZNF705E
SuperfamilyA8MWA4
Peptide AtlasA8MWA4
IPIIPI00739082   IPI00888168   
Protein Interaction databases
DIP (DOE-UCLA)A8MWA4
IntAct (EBI)A8MWA4
BioGRIDZNF705E
STRING (EMBL)ZNF705E
ZODIACZNF705E
Ontologies - Pathways
QuickGOA8MWA4
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 NetworkZNF705E
Atlas of Cancer Signalling NetworkZNF705E
Wikipedia pathwaysZNF705E
Orthology - Evolution
OrthoDB100131539
Phylogenetic Trees/Animal Genes : TreeFamZNF705E
HOVERGENA8MWA4
HOGENOMA8MWA4
Homologs : HomoloGeneZNF705E
Homology/Alignments : Family Browser (UCSC)ZNF705E
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF705E [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF705E
dbVarZNF705E
ClinVarZNF705E
1000_GenomesZNF705E 
Exome Variant ServerZNF705E
ExAC (Exome Aggregation Consortium)ZNF705E (select the gene name)
Genetic variants : HAPMAP100131539
Genomic Variants (DGV)ZNF705E [DGVbeta]
DECIPHER (Syndromes)11:71525091-71532593  
CONAN: Copy Number AnalysisZNF705E 
Mutations
ICGC Data PortalZNF705E 
TCGA Data PortalZNF705E 
Broad Tumor PortalZNF705E
OASIS PortalZNF705E [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDZNF705E
BioMutasearch ZNF705E
DgiDB (Drug Gene Interaction Database)ZNF705E
DoCM (Curated mutations)ZNF705E (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF705E (select a term)
intoGenZNF705E
Cancer3DZNF705E(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF705E
Genetic Testing Registry ZNF705E
NextProtA8MWA4 [Medical]
TSGene100131539
GENETestsZNF705E
Huge Navigator ZNF705E [HugePedia]
snp3D : Map Gene to Disease100131539
BioCentury BCIQZNF705E
ClinGenZNF705E
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100131539
Clinical trialZNF705E
Miscellaneous
canSAR (ICR)ZNF705E (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF705E
EVEXZNF705E
GoPubMedZNF705E
iHOPZNF705E
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:53:42 CET 2017

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