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ZNF697 (zinc finger protein 697)

Identity

Alias_symbol (synonym)MGC45731
Other alias-
HGNC (Hugo) ZNF697
LocusID (NCBI) 90874
Atlas_Id 76338
Location 1p12  [Link to chromosome band 1p12]
Location_base_pair Starts at 119619377 and ends at 119647767 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)
ZNF697 (1p12) / ZNF697 (1p12)

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)ZNF697   32034
Cards
Entrez_Gene (NCBI)ZNF697  90874  zinc finger protein 697
Aliases
GeneCards (Weizmann)ZNF697
Ensembl hg19 (Hinxton)ENSG00000143067 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000143067 [Gene_View]  chr1:119619377-119647767 [Contig_View]  ZNF697 [Vega]
ICGC DataPortalENSG00000143067
TCGA cBioPortalZNF697
AceView (NCBI)ZNF697
Genatlas (Paris)ZNF697
WikiGenes90874
SOURCE (Princeton)ZNF697
Genetics Home Reference (NIH)ZNF697
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF697  -     chr1:119619377-119647767 -  1p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF697  -     1p12   [Description]    (hg19-Feb_2009)
EnsemblZNF697 - 1p12 [CytoView hg19]  ZNF697 - 1p12 [CytoView hg38]
Mapping of homologs : NCBIZNF697 [Mapview hg19]  ZNF697 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK027019 AK311787 BC007260 BC033126 BC063670
RefSeq transcript (Entrez)NM_001080470
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF697
Cluster EST : UnigeneHs.381105 [ NCBI ]
CGAP (NCI)Hs.381105
Alternative Splicing GalleryENSG00000143067
Gene ExpressionZNF697 [ NCBI-GEO ]   ZNF697 [ EBI - ARRAY_EXPRESS ]   ZNF697 [ SEEK ]   ZNF697 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF697 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)90874
GTEX Portal (Tissue expression)ZNF697
Human Protein AtlasENSG00000143067-ZNF697 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5TEC3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5TEC3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5TEC3
Splice isoforms : SwissVarQ5TEC3
PhosPhoSitePlusQ5TEC3
Domaine pattern : Prosite (Expaxy)ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)Znf_C2H2    Znf_C2H2-like    Znf_C2H2/integrase_DNA-bd   
Domain families : Pfam (Sanger)zf-C2H2 (PF00096)   
Domain families : Pfam (NCBI)pfam00096   
Domain families : Smart (EMBL)ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF697
DMDM Disease mutations90874
Blocks (Seattle)ZNF697
SuperfamilyQ5TEC3
Human Protein Atlas [tissue]ENSG00000143067-ZNF697 [tissue]
Peptide AtlasQ5TEC3
IPIIPI00397781   
Protein Interaction databases
DIP (DOE-UCLA)Q5TEC3
IntAct (EBI)Q5TEC3
FunCoupENSG00000143067
BioGRIDZNF697
STRING (EMBL)ZNF697
ZODIACZNF697
Ontologies - Pathways
QuickGOQ5TEC3
Ontology : AmiGOmolecular_function  DNA binding  cellular_component  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  biological_process  metal ion binding  
Ontology : EGO-EBImolecular_function  DNA binding  cellular_component  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  biological_process  metal ion binding  
NDEx NetworkZNF697
Atlas of Cancer Signalling NetworkZNF697
Wikipedia pathwaysZNF697
Orthology - Evolution
OrthoDB90874
GeneTree (enSembl)ENSG00000143067
Phylogenetic Trees/Animal Genes : TreeFamZNF697
HOVERGENQ5TEC3
HOGENOMQ5TEC3
Homologs : HomoloGeneZNF697
Homology/Alignments : Family Browser (UCSC)ZNF697
Gene fusions - Rearrangements
Tumor Fusion PortalZNF697
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF697 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF697
dbVarZNF697
ClinVarZNF697
1000_GenomesZNF697 
Exome Variant ServerZNF697
ExAC (Exome Aggregation Consortium)ENSG00000143067
GNOMAD BrowserENSG00000143067
Genetic variants : HAPMAP90874
Genomic Variants (DGV)ZNF697 [DGVbeta]
DECIPHERZNF697 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF697 
Mutations
ICGC Data PortalZNF697 
TCGA Data PortalZNF697 
Broad Tumor PortalZNF697
OASIS PortalZNF697 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF697  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF697
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ZNF697
DgiDB (Drug Gene Interaction Database)ZNF697
DoCM (Curated mutations)ZNF697 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF697 (select a term)
intoGenZNF697
Cancer3DZNF697(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETZNF697
MedgenZNF697
Genetic Testing Registry ZNF697
NextProtQ5TEC3 [Medical]
TSGene90874
GENETestsZNF697
Target ValidationZNF697
Huge Navigator ZNF697 [HugePedia]
snp3D : Map Gene to Disease90874
BioCentury BCIQZNF697
ClinGenZNF695=/\R>
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD90874
Chemical/Pharm GKB GenePA142670495
Clinical trialZNF697
Miscellaneous
canSAR (ICR)ZNF697 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF697
EVEXZNF697
GoPubMedZNF697
iHOPZNF697
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Nov 20 20:23:43 CET 2017

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