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ZNF705G (zinc finger protein 705G)

Identity

Other alias-
HGNC (Hugo) ZNF705G
LocusID (NCBI) 100131980
Atlas_Id 76348
Location 8p23.1  [Link to chromosome band 8p23]
Location_base_pair Starts at 7357976 and ends at 7362968 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)ZNF705G   37134
Cards
Entrez_Gene (NCBI)ZNF705G  100131980  zinc finger protein 705G
Aliases
GeneCards (Weizmann)ZNF705G
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr8:7357976-7362968 [Contig_View]  ZNF705G [Vega]
TCGA cBioPortalZNF705G
AceView (NCBI)ZNF705G
Genatlas (Paris)ZNF705G
WikiGenes100131980
SOURCE (Princeton)ZNF705G
Genetics Home Reference (NIH)ZNF705G
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF705G  -     chr8:7357976-7362968 -  8p23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF705G  -     8p23.1   [Description]    (hg19-Feb_2009)
EnsemblZNF705G - 8p23.1 [CytoView hg19]  ZNF705G - 8p23.1 [CytoView hg38]
Mapping of homologs : NCBIZNF705G [Mapview hg19]  ZNF705G [Mapview hg38]
Gene and transcription
Genbank (Entrez)BE466749 BF509407
RefSeq transcript (Entrez)NM_001164457
RefSeq genomic (Entrez)NC_000008 NC_018919 NT_187570
Consensus coding sequences : CCDS (NCBI)ZNF705G
Cluster EST : UnigeneHs.528391 [ NCBI ]
CGAP (NCI)Hs.528391
Gene ExpressionZNF705G [ NCBI-GEO ]   ZNF705G [ EBI - ARRAY_EXPRESS ]   ZNF705G [ SEEK ]   ZNF705G [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF705G [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100131980
GTEX Portal (Tissue expression)ZNF705G
Protein : pattern, domain, 3D structure
UniProt/SwissProtA8MUZ8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA8MUZ8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA8MUZ8
Splice isoforms : SwissVarA8MUZ8
PhosPhoSitePlusA8MUZ8
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)   
Domain families : Pfam (NCBI)pfam01352   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF705G
DMDM Disease mutations100131980
Blocks (Seattle)ZNF705G
SuperfamilyA8MUZ8
Peptide AtlasA8MUZ8
IPIIPI00886806   
Protein Interaction databases
DIP (DOE-UCLA)A8MUZ8
IntAct (EBI)A8MUZ8
BioGRIDZNF705G
STRING (EMBL)ZNF705G
ZODIACZNF705G
Ontologies - Pathways
QuickGOA8MUZ8
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 NetworkZNF705G
Atlas of Cancer Signalling NetworkZNF705G
Wikipedia pathwaysZNF705G
Orthology - Evolution
OrthoDB100131980
Phylogenetic Trees/Animal Genes : TreeFamZNF705G
HOVERGENA8MUZ8
HOGENOMA8MUZ8
Homologs : HomoloGeneZNF705G
Homology/Alignments : Family Browser (UCSC)ZNF705G
Gene fusions - Rearrangements
Fusion: Tumor Portal ZNF705G
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF705G [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF705G
dbVarZNF705G
ClinVarZNF705G
1000_GenomesZNF705G 
Exome Variant ServerZNF705G
ExAC (Exome Aggregation Consortium)
Genetic variants : HAPMAP100131980
Genomic Variants (DGV)ZNF705G [DGVbeta]
DECIPHERZNF705G [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF705G 
Mutations
ICGC Data PortalZNF705G 
TCGA Data PortalZNF705G 
Broad Tumor PortalZNF705G
OASIS PortalZNF705G [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF705G  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF705G
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 ZNF705G
DgiDB (Drug Gene Interaction Database)ZNF705G
DoCM (Curated mutations)ZNF705G (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF705G (select a term)
intoGenZNF705G
Cancer3DZNF705G(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF705G
Genetic Testing Registry ZNF705G
NextProtA8MUZ8 [Medical]
TSGene100131980
GENETestsZNF705G
Target ValidationZNF705G
Huge Navigator ZNF705G [HugePedia]
snp3D : Map Gene to Disease100131980
BioCentury BCIQZNF705G
ClinGenZNF705G
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100131980
Chemical/Pharm GKB GenePA165586029
Clinical trialZNF705G
Miscellaneous
canSAR (ICR)ZNF705G (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF705G
EVEXZNF705G
GoPubMedZNF705G
iHOPZNF705G
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Nov 9 12:37:45 CET 2017

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