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ZNF705D (zinc finger protein 705D)

Identity

Other aliasZNF705C
HGNC (Hugo) ZNF705D
LocusID (NCBI) 728957
Atlas_Id 76346
Location 8p23.1  [Link to chromosome band 8p23]
Location_base_pair Starts at 12089338 and ends at 12115516 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)ZNF705D   33202
Cards
Entrez_Gene (NCBI)ZNF705D  728957  zinc finger protein 705D
AliasesZNF705C
GeneCards (Weizmann)ZNF705D
Ensembl hg19 (Hinxton)ENSG00000215343 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000215343 [Gene_View]  chr8:12089338-12115516 [Contig_View]  ZNF705D [Vega]
ICGC DataPortalENSG00000215343
TCGA cBioPortalZNF705D
AceView (NCBI)ZNF705D
Genatlas (Paris)ZNF705D
WikiGenes728957
SOURCE (Princeton)ZNF705D
Genetics Home Reference (NIH)ZNF705D
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF705D  -     chr8:12089338-12115516 +  8p23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF705D  -     8p23.1   [Description]    (hg19-Feb_2009)
EnsemblZNF705D - 8p23.1 [CytoView hg19]  ZNF705D - 8p23.1 [CytoView hg38]
Mapping of homologs : NCBIZNF705D [Mapview hg19]  ZNF705D [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC110823
RefSeq transcript (Entrez)NM_001039615
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF705D
Cluster EST : UnigeneHs.652228 [ NCBI ]
CGAP (NCI)Hs.652228
Alternative Splicing GalleryENSG00000215343
Gene ExpressionZNF705D [ NCBI-GEO ]   ZNF705D [ EBI - ARRAY_EXPRESS ]   ZNF705D [ SEEK ]   ZNF705D [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF705D [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)728957
GTEX Portal (Tissue expression)ZNF705D
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0CH99   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0CH99  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0CH99
Splice isoforms : SwissVarP0CH99
PhosPhoSitePlusP0CH99
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)   
Domain families : Pfam (NCBI)pfam01352    pfam00096   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF705D
DMDM Disease mutations728957
Blocks (Seattle)ZNF705D
SuperfamilyP0CH99
Human Protein AtlasENSG00000215343
Peptide AtlasP0CH99
IPIIPI00970847   
Protein Interaction databases
DIP (DOE-UCLA)P0CH99
IntAct (EBI)P0CH99
FunCoupENSG00000215343
BioGRIDZNF705D
STRING (EMBL)ZNF705D
ZODIACZNF705D
Ontologies - Pathways
QuickGOP0CH99
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 NetworkZNF705D
Atlas of Cancer Signalling NetworkZNF705D
Wikipedia pathwaysZNF705D
Orthology - Evolution
OrthoDB728957
GeneTree (enSembl)ENSG00000215343
Phylogenetic Trees/Animal Genes : TreeFamZNF705D
HOVERGENP0CH99
HOGENOMP0CH99
Homologs : HomoloGeneZNF705D
Homology/Alignments : Family Browser (UCSC)ZNF705D
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF705D [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF705D
dbVarZNF705D
ClinVarZNF705D
1000_GenomesZNF705D 
Exome Variant ServerZNF705D
ExAC (Exome Aggregation Consortium)ZNF705D (select the gene name)
Genetic variants : HAPMAP728957
Genomic Variants (DGV)ZNF705D [DGVbeta]
DECIPHERZNF705D [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF705D 
Mutations
ICGC Data PortalZNF705D 
TCGA Data PortalZNF705D 
Broad Tumor PortalZNF705D
OASIS PortalZNF705D [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF705D  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF705D
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ZNF705D
DgiDB (Drug Gene Interaction Database)ZNF705D
DoCM (Curated mutations)ZNF705D (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF705D (select a term)
intoGenZNF705D
Cancer3DZNF705D(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF705D
Genetic Testing Registry ZNF705D
NextProtP0CH99 [Medical]
TSGene728957
GENETestsZNF705D
Target ValidationZNF705D
Huge Navigator ZNF705D [HugePedia]
snp3D : Map Gene to Disease728957
BioCentury BCIQZNF705D
ClinGenZNF705D
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD728957
Chemical/Pharm GKB GenePA162410210
Clinical trialZNF705D
Miscellaneous
canSAR (ICR)ZNF705D (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF705D
EVEXZNF705D
GoPubMedZNF705D
iHOPZNF705D
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 15:51:06 CEST 2017

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