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ZNF765-ZNF761 (ZNF765-ZNF761 readthrough)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 110116772
Atlas_Id 79904
Location 19q13.42  [Link to chromosome band 19q13]
Location_base_pair Starts at 53395133 and ends at 53458261 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)ZNF765-ZNF761  110116772  ZNF765-ZNF761 readthrough
Aliases
GeneCards (Weizmann)ZNF765-ZNF761
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr19:53395133-53458261 [Contig_View]  ZNF765-ZNF761 [Vega]
TCGA cBioPortalZNF765-ZNF761
AceView (NCBI)ZNF765-ZNB761<-a.
Genatlas (Paris)ZNF765-ZNF761
WikiGenes110116772
SOURCE (Princeton)ZNF765-ZNF761
Genetics Home Reference (NIH)ZNF765-ZNF761
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF765-ZNF761  -     chr19:53395133-53458261 +  19q13.42   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF765-ZNF761  -     19q13.42   [Description]    (hg19-Feb_2009)
EnsemblZNF765-ZNF761 - 19q13.42 [CytoView hg19]  ZNF765-ZNF761 - 19q13.42 [CytoView hg38]
Mapping of homologs : NCBIZNF765-ZNF761 [Mapview hg19]  ZNF765-ZNF761 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001350496
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF765-ZNF761
Gene ExpressionZNF765-ZNF761 [ NCBI-GEO ]   ZNF765-ZNF761 [ EBI - ARRAY_EXPRESS ]   ZNF765-ZNF761 [ SEEK ]   ZNF765-ZNF761 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF765-ZNF761 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)110116772
GTEX Portal (Tissue expression)ZNF765-ZNF761
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ86XN6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ86XN6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ86XN6
Splice isoforms : SwissVarQ86XN6
PhosPhoSitePlusQ86XN6
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)    zf-C2H2_6 (PF13912)   
Domain families : Pfam (NCBI)pfam01352    pfam00096    pfam13912   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF765-ZNF761
DMDM Disease mutations110116772
Blocks (Seattle)ZNF765-ZNF761
SuperfamilyQ86XN6
Peptide AtlasQ86XN6
Protein Interaction databases
DIP (DOE-UCLA)Q86XN6
IntAct (EBI)Q86XN6
BioGRIDZNF765-ZNF761
STRING (EMBL)ZNF765-ZNF761
ZODIACZNF765-ZNF761
Ontologies - Pathways
QuickGOQ86XN6
Ontology : AmiGODNA binding  transcription factor activity, sequence-specific DNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
Ontology : EGO-EBIDNA binding  transcription factor activity, sequence-specific DNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
NDEx NetworkZNF765-ZNF761
Atlas of Cancer Signalling NetworkZNF765-ZNF761
Wikipedia pathwaysZNF765-ZNF761
Orthology - Evolution
OrthoDB110116772
Phylogenetic Trees/Animal Genes : TreeFam-
HOVERGENQ86XN6
HOGENOMQ86XN6
Homologs : HomoloGeneZNF765-ZNF761
Homology/Alignments : Family Browser (UCSC)ZNF765-ZNF761
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF765-ZNF761 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF765-ZNF761
dbVarZNF765-ZNF761
ClinVarZNF765-ZNF761
1000_GenomesZNF765-ZNF761 
Exome Variant ServerZNF765-ZNF761
ExAC (Exome Aggregation Consortium)ZNF765-ZNF761 (select the gene name)
Genetic variants : HAPMAP110116772
Genomic Variants (DGV)ZNF765-ZNF761 [DGVbeta]
DECIPHERZNF765-ZNF761 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF765-ZNF761 
Mutations
ICGC Data Portal- 
TCGA Data Portal- 
Broad Tumor Portal-
OASIS Portal- [ Somatic mutations - Copy number]
Mutations and Diseases : HGMD-
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 ZNF765-ZNF761
DgiDB (Drug Gene Interaction Database)ZNF765-ZNF761
DoCM (Curated mutations)ZNF765-ZNF761 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF765-ZNF761 (select a term)
intoGenZNF765-ZNF761
Cancer3DZNF765-ZNF761(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF765-ZNF761
Genetic Testing Registry ZNF765-ZNF761
NextProtQ86XN6 [Medical]
TSGene110116772
GENETestsZNF765-ZNF761
Target ValidationZNF765-ZNF761
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease110116772
BioCentury BCIQZNF765-ZNF761
ClinGenZNF765-ZNF761
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD110116772
Clinical trialZNF765-ZNF761
Miscellaneous
canSAR (ICR)ZNF765-ZNF761 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF765-ZNF761
EVEXZNF765-ZNF761
GoPubMedZNF765-ZNF761
iHOPZNF765-ZNF761
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 13:45:17 CEST 2017

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