Atlas of Genetics and Cytogenetics in Oncology and Haematology


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ZNF723 (zinc finger protein 723)

Identity

Alias_namesZNF723P
zinc finger protein 723, pseudogene
Other alias
HGNC (Hugo) ZNF723
LocusID (NCBI) 646864
Atlas_Id 79909
Location 19p12  [Link to chromosome band 19p12]
Location_base_pair Starts at 22832321 and ends at 22858667 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)ZNF723   32286
Cards
Entrez_Gene (NCBI)ZNF723  646864  zinc finger protein 723
AliasesZNF723P
GeneCards (Weizmann)ZNF723
Ensembl hg19 (Hinxton)ENSG00000268696 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000268696 [Gene_View]  ENSG00000268696 [Sequence]  chr19:22832321-22858667 [Contig_View]  ZNF723 [Vega]
ICGC DataPortalENSG00000268696
TCGA cBioPortalZNF723
AceView (NCBI)ZNF723
Genatlas (Paris)ZNF723
WikiGenes646864
SOURCE (Princeton)ZNF723
Genetics Home Reference (NIH)ZNF723
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF723  -     chr19:22832321-22858667 +  19p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF723  -     19p12   [Description]    (hg19-Feb_2009)
GoldenPathZNF723 - 19p12 [CytoView hg19]  ZNF723 - 19p12 [CytoView hg38]
ImmunoBaseENSG00000268696
Mapping of homologs : NCBIZNF723 [Mapview hg19]  ZNF723 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001349726
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF723
Alternative Splicing GalleryENSG00000268696
Gene ExpressionZNF723 [ NCBI-GEO ]   ZNF723 [ EBI - ARRAY_EXPRESS ]   ZNF723 [ SEEK ]   ZNF723 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF723 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)646864
GTEX Portal (Tissue expression)ZNF723
Human Protein AtlasENSG00000268696-ZNF723 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0DPD5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0DPD5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0DPD5
Splice isoforms : SwissVarP0DPD5
PhosPhoSitePlusP0DPD5
Domaine pattern : Prosite (Expaxy)KRAB (PS50805)    ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)KRAB    KRAB_dom_sf    Znf_C2H2_sf    Znf_C2H2_type   
Domain families : Pfam (Sanger)KRAB (PF01352)   
Domain families : Pfam (NCBI)pfam01352   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF723
DMDM Disease mutations646864
Blocks (Seattle)ZNF723
SuperfamilyP0DPD5
Human Protein Atlas [tissue]ENSG00000268696-ZNF723 [tissue]
Peptide AtlasP0DPD5
Protein Interaction databases
DIP (DOE-UCLA)P0DPD5
IntAct (EBI)P0DPD5
FunCoupENSG00000268696
BioGRIDZNF723
STRING (EMBL)ZNF723
ZODIACZNF723
Ontologies - Pathways
QuickGOP0DPD5
Ontology : AmiGODNA binding  nucleus  regulation of transcription, DNA-templated  metal ion binding  
Ontology : EGO-EBIDNA binding  nucleus  regulation of transcription, DNA-templated  metal ion binding  
NDEx NetworkZNF723
Atlas of Cancer Signalling NetworkZNF723
Wikipedia pathwaysZNF723
Orthology - Evolution
OrthoDB646864
GeneTree (enSembl)ENSG00000268696
Phylogenetic Trees/Animal Genes : TreeFamZNF723
HOGENOMP0DPD5
Homologs : HomoloGeneZNF723
Homology/Alignments : Family Browser (UCSC)ZNF723
Gene fusions - Rearrangements
Fusion : QuiverZNF723
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF723 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF723
dbVarZNF723
ClinVarZNF723
1000_GenomesZNF723 
Exome Variant ServerZNF723
ExAC (Exome Aggregation Consortium)ENSG00000268696
GNOMAD BrowserENSG00000268696
Varsome BrowserZNF723
Genetic variants : HAPMAP646864
Genomic Variants (DGV)ZNF723 [DGVbeta]
DECIPHERZNF723 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF723 
Mutations
ICGC Data PortalZNF723 
TCGA Data PortalZNF723 
Broad Tumor PortalZNF723
OASIS PortalZNF723 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDZNF723
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 ZNF723
DgiDB (Drug Gene Interaction Database)ZNF723
DoCM (Curated mutations)ZNF723 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF723 (select a term)
intoGenZNF723
Cancer3DZNF723(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETZNF723
MedgenZNF723
Genetic Testing Registry ZNF723
NextProtP0DPD5 [Medical]
TSGene646864
GENETestsZNF723
Target ValidationZNF723
Huge Navigator ZNF723 [HugePedia]
snp3D : Map Gene to Disease646864
BioCentury BCIQZNF723
ClinGenZNF723
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD646864
Clinical trialZNF723
Miscellaneous
canSAR (ICR)ZNF723 (select the gene name)
DataMed IndexZNF723
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF723
EVEXZNF723
GoPubMedZNF723
iHOPZNF723
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Aug 12 16:58:19 CEST 2019

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