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ZNF707 (zinc finger protein 707)

Identity

Other alias-
HGNC (Hugo) ZNF707
LocusID (NCBI) 286075
Atlas_Id 76350
Location 8q24.3  [Link to chromosome band 8q24]
Location_base_pair Starts at 144766622 and ends at 144777555 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)ZNF707   27815
Cards
Entrez_Gene (NCBI)ZNF707  286075  zinc finger protein 707
Aliases
GeneCards (Weizmann)ZNF707
Ensembl hg19 (Hinxton)ENSG00000181135 [Gene_View]  chr8:144766622-144777555 [Contig_View]  ZNF707 [Vega]
Ensembl hg38 (Hinxton)ENSG00000181135 [Gene_View]  chr8:144766622-144777555 [Contig_View]  ZNF707 [Vega]
ICGC DataPortalENSG00000181135
TCGA cBioPortalZNF707
AceView (NCBI)ZNF707
Genatlas (Paris)ZNF707
WikiGenes286075
SOURCE (Princeton)ZNF707
Genetics Home Reference (NIH)ZNF707
Genomic and cartography
GoldenPath hg19 (UCSC)ZNF707  -     chr8:144766622-144777555 +  8q24.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ZNF707  -     8q24.3   [Description]    (hg38-Dec_2013)
EnsemblZNF707 - 8q24.3 [CytoView hg19]  ZNF707 - 8q24.3 [CytoView hg38]
Mapping of homologs : NCBIZNF707 [Mapview hg19]  ZNF707 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK001126 AK055198 AK055263 AK095138 AK290432
RefSeq transcript (Entrez)NM_001100598 NM_001100599 NM_001288805 NM_001288806 NM_001288807 NM_001288808 NM_001288809 NM_173831
RefSeq genomic (Entrez)NC_000008 NC_018919 NT_008046 NT_187571 NW_004929340
Consensus coding sequences : CCDS (NCBI)ZNF707
Cluster EST : UnigeneHs.521922 [ NCBI ]
CGAP (NCI)Hs.521922
Alternative Splicing GalleryENSG00000181135
Gene ExpressionZNF707 [ NCBI-GEO ]   ZNF707 [ EBI - ARRAY_EXPRESS ]   ZNF707 [ SEEK ]   ZNF707 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF707 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)286075
GTEX Portal (Tissue expression)ZNF707
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96C28   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96C28  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96C28
Splice isoforms : SwissVarQ96C28
PhosPhoSitePlusQ96C28
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)    zf-C2H2 (PF00096)   
Domain families : Pfam (NCBI)pfam01352    pfam00096   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF707
DMDM Disease mutations286075
Blocks (Seattle)ZNF707
SuperfamilyQ96C28
Human Protein AtlasENSG00000181135
Peptide AtlasQ96C28
HPRD14162
IPIIPI00395701   IPI00890722   IPI00978784   IPI00984762   IPI00983137   IPI00982758   IPI00982868   IPI00982211   IPI00981088   
Protein Interaction databases
DIP (DOE-UCLA)Q96C28
IntAct (EBI)Q96C28
FunCoupENSG00000181135
BioGRIDZNF707
STRING (EMBL)ZNF707
ZODIACZNF707
Ontologies - Pathways
QuickGOQ96C28
Ontology : AmiGODNA binding  protein binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
Ontology : EGO-EBIDNA binding  protein binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
NDEx NetworkZNF707
Atlas of Cancer Signalling NetworkZNF707
Wikipedia pathwaysZNF707
Orthology - Evolution
OrthoDB286075
GeneTree (enSembl)ENSG00000181135
Phylogenetic Trees/Animal Genes : TreeFamZNF707
HOVERGENQ96C28
HOGENOMQ96C28
Homologs : HomoloGeneZNF707
Homology/Alignments : Family Browser (UCSC)ZNF707
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF707 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF707
dbVarZNF707
ClinVarZNF707
1000_GenomesZNF707 
Exome Variant ServerZNF707
ExAC (Exome Aggregation Consortium)ZNF707 (select the gene name)
Genetic variants : HAPMAP286075
Genomic Variants (DGV)ZNF707 [DGVbeta]
DECIPHER (Syndromes)8:144766622-144777555  ENSG00000181135
CONAN: Copy Number AnalysisZNF707 
Mutations
ICGC Data PortalZNF707 
TCGA Data PortalZNF707 
Broad Tumor PortalZNF707
OASIS PortalZNF707 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF707  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF707
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ZNF707
DgiDB (Drug Gene Interaction Database)ZNF707
DoCM (Curated mutations)ZNF707 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF707 (select a term)
intoGenZNF707
Cancer3DZNF707(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF707
Genetic Testing Registry ZNF707
NextProtQ96C28 [Medical]
TSGene286075
GENETestsZNF707
Huge Navigator ZNF707 [HugePedia]
snp3D : Map Gene to Disease286075
BioCentury BCIQZNF707
ClinGenZNF707
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD286075
Chemical/Pharm GKB GenePA142670506
Clinical trialZNF707
Miscellaneous
canSAR (ICR)ZNF707 (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF707
EVEXZNF707
GoPubMedZNF707
iHOPZNF707
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 12:53:43 CET 2017

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