Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

ZNF814 (zinc finger protein 814)

Identity

Other alias-
HGNC (Hugo) ZNF814
LocusID (NCBI) 730051
Atlas_Id 76423
Location 19q13.43  [Link to chromosome band 19q13]
Location_base_pair Starts at 57869379 and ends at 57889074 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
ZNF814 (19q13.43) / IRF3 (19q13.33)ZNF814 (19q13.43) / PIK3CD (1p36.22)ZNF814 (19q13.43) / TNRC6A (16p12.1)
ZNF814 (19q13.43) / USF1 (1q23.3)ZNF814 (19q13.43) / ZNF814 (19q13.43)

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)ZNF814   33258
Cards
Entrez_Gene (NCBI)ZNF814  730051  zinc finger protein 814
Aliases
GeneCards (Weizmann)ZNF814
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr19:57869379-57889074 [Contig_View]  ZNF814 [Vega]
TCGA cBioPortalZNF814
AceView (NCBI)ZNF814
Genatlas (Paris)ZNF814
WikiGenes730051
SOURCE (Princeton)ZNF814
Genetics Home Reference (NIH)ZNF814
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF814  -     chr19:57869379-57889074 -  19q13.43   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF814  -     19q13.43   [Description]    (hg19-Feb_2009)
EnsemblZNF814 - 19q13.43 [CytoView hg19]  ZNF814 - 19q13.43 [CytoView hg38]
Mapping of homologs : NCBIZNF814 [Mapview hg19]  ZNF814 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF086563 AK022663 AK091350 AK096401 AK300483
RefSeq transcript (Entrez)NM_001144989
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF814
Cluster EST : UnigeneHs.733810 [ NCBI ]
CGAP (NCI)Hs.733810
Gene ExpressionZNF814 [ NCBI-GEO ]   ZNF814 [ EBI - ARRAY_EXPRESS ]   ZNF814 [ SEEK ]   ZNF814 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF814 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)730051
GTEX Portal (Tissue expression)ZNF814
Protein : pattern, domain, 3D structure
UniProt/SwissProtB7Z6K7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtB7Z6K7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProB7Z6K7
Splice isoforms : SwissVarB7Z6K7
PhosPhoSitePlusB7Z6K7
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)ZNF814
DMDM Disease mutations730051
Blocks (Seattle)ZNF814
SuperfamilyB7Z6K7
Peptide AtlasB7Z6K7
IPIIPI00477965   IPI00940769   IPI00878321   
Protein Interaction databases
DIP (DOE-UCLA)B7Z6K7
IntAct (EBI)B7Z6K7
BioGRIDZNF814
STRING (EMBL)ZNF814
ZODIACZNF814
Ontologies - Pathways
QuickGOB7Z6K7
Ontology : AmiGOnucleic acid binding  intracellular  negative regulation of transcription, DNA-templated  metal ion binding  
Ontology : EGO-EBInucleic acid binding  intracellular  negative regulation of transcription, DNA-templated  metal ion binding  
NDEx NetworkZNF814
Atlas of Cancer Signalling NetworkZNF814
Wikipedia pathwaysZNF814
Orthology - Evolution
OrthoDB730051
Phylogenetic Trees/Animal Genes : TreeFamZNF814
HOVERGENB7Z6K7
HOGENOMB7Z6K7
Homologs : HomoloGeneZNF814
Homology/Alignments : Family Browser (UCSC)ZNF814
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF814 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF814
dbVarZNF814
ClinVarZNF814
1000_GenomesZNF814 
Exome Variant ServerZNF814
ExAC (Exome Aggregation Consortium)ZNF814 (select the gene name)
Genetic variants : HAPMAP730051
Genomic Variants (DGV)ZNF814 [DGVbeta]
DECIPHERZNF814 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF814 
Mutations
ICGC Data PortalZNF814 
TCGA Data PortalZNF814 
Broad Tumor PortalZNF814
OASIS PortalZNF814 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF814  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF814
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 ZNF814
DgiDB (Drug Gene Interaction Database)ZNF814
DoCM (Curated mutations)ZNF814 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF814 (select a term)
intoGenZNF814
Cancer3DZNF814(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF814
Genetic Testing Registry ZNF814
NextProtB7Z6K7 [Medical]
TSGene730051
GENETestsZNF814
Huge Navigator ZNF814 [HugePedia]
snp3D : Map Gene to Disease730051
BioCentury BCIQZNF814
ClinGenZNF814
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD730051
Chemical/Pharm GKB GenePA164727759
Clinical trialZNF814
Miscellaneous
canSAR (ICR)ZNF814 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF814
EVEXZNF814
GoPubMedZNF814
iHOPZNF814
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Fri May 19 12:03:57 CEST 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.