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ZNF766 (zinc finger protein 766)

Identity

Other alias-
HGNC (Hugo) ZNF766
LocusID (NCBI) 90321
Atlas_Id 76384
Location 19q13.41  [Link to chromosome band 19q13]
Location_base_pair Starts at 52269571 and ends at 52292723 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
ZNF766 (19q13.41) / ITPR2 (12p12.1)

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)ZNF766   28063
Cards
Entrez_Gene (NCBI)ZNF766  90321  zinc finger protein 766
Aliases
GeneCards (Weizmann)ZNF766
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr19:52269571-52292723 [Contig_View]  ZNF766 [Vega]
TCGA cBioPortalZNF766
AceView (NCBI)ZNF766
Genatlas (Paris)ZNF766
WikiGenes90321
SOURCE (Princeton)ZNF766
Genetics Home Reference (NIH)ZNF766
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF766  -     chr19:52269571-52292723 +  19q13.41   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF766  -     19q13.41   [Description]    (hg19-Feb_2009)
EnsemblZNF766 - 19q13.41 [CytoView hg19]  ZNF766 - 19q13.41 [CytoView hg38]
Mapping of homologs : NCBIZNF766 [Mapview hg19]  ZNF766 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK022545 AK024074 AK024268 AK097729 BC109201
RefSeq transcript (Entrez)NM_001010851
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF766
Cluster EST : UnigeneHs.439662 [ NCBI ]
CGAP (NCI)Hs.439662
Gene ExpressionZNF766 [ NCBI-GEO ]   ZNF766 [ EBI - ARRAY_EXPRESS ]   ZNF766 [ SEEK ]   ZNF766 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF766 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)90321
GTEX Portal (Tissue expression)ZNF766
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5HY98   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5HY98  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5HY98
Splice isoforms : SwissVarQ5HY98
PhosPhoSitePlusQ5HY98
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)ZNF766
DMDM Disease mutations90321
Blocks (Seattle)ZNF766
SuperfamilyQ5HY98
Peptide AtlasQ5HY98
HPRD14268
IPIIPI00375655   IPI00940215   
Protein Interaction databases
DIP (DOE-UCLA)Q5HY98
IntAct (EBI)Q5HY98
BioGRIDZNF766
STRING (EMBL)ZNF766
ZODIACZNF766
Ontologies - Pathways
QuickGOQ5HY98
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 NetworkZNF766
Atlas of Cancer Signalling NetworkZNF766
Wikipedia pathwaysZNF766
Orthology - Evolution
OrthoDB90321
Phylogenetic Trees/Animal Genes : TreeFamZNF766
HOVERGENQ5HY98
HOGENOMQ5HY98
Homologs : HomoloGeneZNF766
Homology/Alignments : Family Browser (UCSC)ZNF766
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF766 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF766
dbVarZNF766
ClinVarZNF766
1000_GenomesZNF766 
Exome Variant ServerZNF766
ExAC (Exome Aggregation Consortium)ZNF766 (select the gene name)
Genetic variants : HAPMAP90321
Genomic Variants (DGV)ZNF766 [DGVbeta]
DECIPHERZNF766 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF766 
Mutations
ICGC Data PortalZNF766 
TCGA Data PortalZNF766 
Broad Tumor PortalZNF766
OASIS PortalZNF766 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF766  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF766
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ZNF766
DgiDB (Drug Gene Interaction Database)ZNF766
DoCM (Curated mutations)ZNF766 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF766 (select a term)
intoGenZNF766
Cancer3DZNF766(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF766
Genetic Testing Registry ZNF766
NextProtQ5HY98 [Medical]
TSGene90321
GENETestsZNF766
Target ValidationZNF766
Huge Navigator ZNF766 [HugePedia]
snp3D : Map Gene to Disease90321
BioCentury BCIQZNF766
ClinGenZNF766
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD90321
Chemical/Pharm GKB GenePA162410313
Clinical trialZNF766
Miscellaneous
canSAR (ICR)ZNF766 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF766
EVEXZNF766
GoPubMedZNF766
iHOPZNF766
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:51:15 CEST 2017

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