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ZNF812 (zinc finger protein 812)

Identity

Other alias-
HGNC (Hugo) ZNF812
LocusID (NCBI) 729648
Atlas_Id 76421
Location 19p13.2  [Link to chromosome band 19p13]
Location_base_pair Starts at 9800814 and ends at 9811493 bp from pter ( according to hg19-Feb_2009)

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)ZNF812   33242
Cards
Entrez_Gene (NCBI)ZNF812  729648  zinc finger protein 812
Aliases
GeneCards (Weizmann)ZNF812
Ensembl hg19 (Hinxton)ENSG00000224689 [Gene_View]  chr19:9800814-9811493 [Contig_View]  ZNF812 [Vega]
Ensembl hg38 (Hinxton)ENSG00000224689 [Gene_View]  chr19:9800814-9811493 [Contig_View]  ZNF812 [Vega]
ICGC DataPortalENSG00000224689
TCGA cBioPortalZNF812
AceView (NCBI)ZNF812
Genatlas (Paris)ZNF812
WikiGenes729648
SOURCE (Princeton)ZNF812
Genetics Home Reference (NIH)ZNF812
Genomic and cartography
GoldenPath hg19 (UCSC)ZNF812  -     chr19:9800814-9811493 -  19p13.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ZNF812  -     19p13.2   [Description]    (hg38-Dec_2013)
EnsemblZNF812 - 19p13.2 [CytoView hg19]  ZNF812 - 19p13.2 [CytoView hg38]
Mapping of homologs : NCBIZNF812 [Mapview hg19]  ZNF812 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK296815
RefSeq transcript (Entrez)NM_001199814
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011295 NW_004929414
Consensus coding sequences : CCDS (NCBI)ZNF812
Cluster EST : UnigeneHs.626848 [ NCBI ]
CGAP (NCI)Hs.626848
Alternative Splicing GalleryENSG00000224689
Gene ExpressionZNF812 [ NCBI-GEO ]   ZNF812 [ EBI - ARRAY_EXPRESS ]   ZNF812 [ SEEK ]   ZNF812 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF812 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)729648
GTEX Portal (Tissue expression)ZNF812
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0C7V5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0C7V5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0C7V5
Splice isoforms : SwissVarP0C7V5
PhosPhoSitePlusP0C7V5
Domaine pattern : Prosite (Expaxy)KRAB (PS50805)    ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)Krueppel-associated_box    Znf_C2H2    Znf_C2H2-like    Znf_C2H2/integrase_DNA-bd   
Domain families : Pfam (Sanger)KRAB (PF01352)    zf-C2H2 (PF00096)   
Domain families : Pfam (NCBI)pfam01352    pfam00096   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF812
DMDM Disease mutations729648
Blocks (Seattle)ZNF812
SuperfamilyP0C7V5
Human Protein AtlasENSG00000224689
Peptide AtlasP0C7V5
IPIIPI00247681   
Protein Interaction databases
DIP (DOE-UCLA)P0C7V5
IntAct (EBI)P0C7V5
FunCoupENSG00000224689
BioGRIDZNF812
STRING (EMBL)ZNF812
ZODIACZNF812
Ontologies - Pathways
QuickGOP0C7V5
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 NetworkZNF812
Atlas of Cancer Signalling NetworkZNF812
Wikipedia pathwaysZNF812
Orthology - Evolution
OrthoDB729648
GeneTree (enSembl)ENSG00000224689
Phylogenetic Trees/Animal Genes : TreeFamZNF812
HOVERGENP0C7V5
HOGENOMP0C7V5
Homologs : HomoloGeneZNF812
Homology/Alignments : Family Browser (UCSC)ZNF812
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF812 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF812
dbVarZNF812
ClinVarZNF812
1000_GenomesZNF812 
Exome Variant ServerZNF812
ExAC (Exome Aggregation Consortium)ZNF812 (select the gene name)
Genetic variants : HAPMAP729648
Genomic Variants (DGV)ZNF812 [DGVbeta]
DECIPHER (Syndromes)19:9800814-9811493  ENSG00000224689
CONAN: Copy Number AnalysisZNF812 
Mutations
ICGC Data PortalZNF812 
TCGA Data PortalZNF812 
Broad Tumor PortalZNF812
OASIS PortalZNF812 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF812  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF812
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 ZNF812
DgiDB (Drug Gene Interaction Database)ZNF812
DoCM (Curated mutations)ZNF812 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF812 (select a term)
intoGenZNF812
Cancer3DZNF812(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF812
Genetic Testing Registry ZNF812
NextProtP0C7V5 [Medical]
TSGene729648
GENETestsZNF812
Huge Navigator ZNF812 [HugePedia]
snp3D : Map Gene to Disease729648
BioCentury BCIQZNF812
ClinGenZNF812
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD729648
Chemical/Pharm GKB GenePA162410648
Clinical trialZNF812
Miscellaneous
canSAR (ICR)ZNF812 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF812
EVEXZNF812
GoPubMedZNF812
iHOPZNF812
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:53:58 CET 2017

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