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ZNF207 (zinc finger protein 207)

Identity

Other aliasBuGZ
hBuGZ
HGNC (Hugo) ZNF207
LocusID (NCBI) 7756
Atlas_Id 42874
Location 17q11.2  [Link to chromosome band 17q11]
Location_base_pair Starts at 32350138 and ends at 32370449 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)
EPHA6 (3q11.2) / ZNF207 (17q11.2)GOSR1 (17q11.2) / ZNF207 (17q11.2)TEAD4 (12p13.33) / ZNF207 (17q11.2)
ZNF207 (17q11.2) / C17orf75 (17q11.2)ZNF207 (17q11.2) / ERBB2 (17q12)ZNF207 (17q11.2) / G3BP1 (5q33.1)
ZNF207 (17q11.2) / IL4R (16p12.1)ZNF207 (17q11.2) / PHC1 (12p13.31)ZNF207 (17q11.2) / SSU72 (1p36.33)
ZNF207 (17q11.2) / TNKS1BP1 (11q12.1)ZNF207 (17q11.2) / ZNF207 (17q11.2)ZNF207 17q11.2 / C17orf75 17q11.2

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)ZNF207   12998
Cards
Entrez_Gene (NCBI)ZNF207  7756  zinc finger protein 207
AliasesBuGZ; hBuGZ
GeneCards (Weizmann)ZNF207
Ensembl hg19 (Hinxton)ENSG00000010244 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000010244 [Gene_View]  chr17:32350138-32370449 [Contig_View]  ZNF207 [Vega]
ICGC DataPortalENSG00000010244
TCGA cBioPortalZNF207
AceView (NCBI)ZNF207
Genatlas (Paris)ZNF207
WikiGenes7756
SOURCE (Princeton)ZNF207
Genetics Home Reference (NIH)ZNF207
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF207  -     chr17:32350138-32370449 +  17q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF207  -     17q11.2   [Description]    (hg19-Feb_2009)
EnsemblZNF207 - 17q11.2 [CytoView hg19]  ZNF207 - 17q11.2 [CytoView hg38]
Mapping of homologs : NCBIZNF207 [Mapview hg19]  ZNF207 [Mapview hg38]
OMIM603428   
Gene and transcription
Genbank (Entrez)AB209215 AF046001 AI308956 AK026215 AK226172
RefSeq transcript (Entrez)NM_001032293 NM_001098507 NM_003457
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF207
Cluster EST : UnigeneHs.500775 [ NCBI ]
CGAP (NCI)Hs.500775
Alternative Splicing GalleryENSG00000010244
Gene ExpressionZNF207 [ NCBI-GEO ]   ZNF207 [ EBI - ARRAY_EXPRESS ]   ZNF207 [ SEEK ]   ZNF207 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF207 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)7756
GTEX Portal (Tissue expression)ZNF207
Human Protein AtlasENSG00000010244-ZNF207 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtO43670   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO43670  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO43670
Splice isoforms : SwissVarO43670
PhosPhoSitePlusO43670
Domaine pattern : Prosite (Expaxy)ZINC_FINGER_C2H2_1 (PS00028)   
Domains : Interpro (EBI)Znf_C2H2    Znf_C2H2-like   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Domain families : Smart (EMBL)ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF207
DMDM Disease mutations7756
Blocks (Seattle)ZNF207
SuperfamilyO43670
Human Protein Atlas [tissue]ENSG00000010244-ZNF207 [tissue]
Peptide AtlasO43670
HPRD04576
IPIIPI00013457   IPI00219759   IPI00219760   IPI00925888   IPI00935311   IPI00792837   
Protein Interaction databases
DIP (DOE-UCLA)O43670
IntAct (EBI)O43670
FunCoupENSG00000010244
BioGRIDZNF207
STRING (EMBL)ZNF207
ZODIACZNF207
Ontologies - Pathways
QuickGOO43670
Ontology : AmiGOmitotic sister chromatid segregation  kinetochore  kinetochore  condensed chromosome kinetochore  microtubule bundle formation  DNA binding  transcription factor activity, sequence-specific DNA binding  RNA binding  protein binding  nucleus  nucleus  nucleoplasm  nucleolus  cytoplasm  spindle  microtubule  regulation of transcription, DNA-templated  mitotic spindle assembly checkpoint  microtubule binding  heparin binding  zinc ion binding  attachment of spindle microtubules to kinetochore  microtubule polymerization  protein stabilization  cell division  regulation of chromosome segregation  mitotic spindle assembly  spindle matrix  
Ontology : EGO-EBImitotic sister chromatid segregation  kinetochore  kinetochore  condensed chromosome kinetochore  microtubule bundle formation  DNA binding  transcription factor activity, sequence-specific DNA binding  RNA binding  protein binding  nucleus  nucleus  nucleoplasm  nucleolus  cytoplasm  spindle  microtubule  regulation of transcription, DNA-templated  mitotic spindle assembly checkpoint  microtubule binding  heparin binding  zinc ion binding  attachment of spindle microtubules to kinetochore  microtubule polymerization  protein stabilization  cell division  regulation of chromosome segregation  mitotic spindle assembly  spindle matrix  
NDEx NetworkZNF207
Atlas of Cancer Signalling NetworkZNF207
Wikipedia pathwaysZNF207
Orthology - Evolution
OrthoDB7756
GeneTree (enSembl)ENSG00000010244
Phylogenetic Trees/Animal Genes : TreeFamZNF207
HOVERGENO43670
HOGENOMO43670
Homologs : HomoloGeneZNF207
Homology/Alignments : Family Browser (UCSC)ZNF207
Gene fusions - Rearrangements
Fusion : MitelmanGOSR1/ZNF207 [17q11.2/17q11.2]  [t(17;17)(q11;q11)]  
Fusion : MitelmanZNF207/C17orf75 [17q11.2/17q11.2]  [t(17;17)(q11;q11)]  
Fusion: TCGA_MDACCZNF207 17q11.2 C17orf75 17q11.2 BRCA
Tumor Fusion PortalZNF207
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF207 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF207
dbVarZNF207
ClinVarZNF207
1000_GenomesZNF207 
Exome Variant ServerZNF207
ExAC (Exome Aggregation Consortium)ENSG00000010244
GNOMAD BrowserENSG00000010244
Genetic variants : HAPMAP7756
Genomic Variants (DGV)ZNF207 [DGVbeta]
DECIPHERZNF207 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF207 
Mutations
ICGC Data PortalZNF207 
TCGA Data PortalZNF207 
Broad Tumor PortalZNF207
OASIS PortalZNF207 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF207  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF207
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 ZNF207
DgiDB (Drug Gene Interaction Database)ZNF207
DoCM (Curated mutations)ZNF207 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF207 (select a term)
intoGenZNF207
Cancer3DZNF207(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM603428   
Orphanet
DisGeNETZNF207
MedgenZNF207
Genetic Testing Registry ZNF207
NextProtO43670 [Medical]
TSGene7756
GENETestsZNF207
Target ValidationZNF207
Huge Navigator ZNF207 [HugePedia]
snp3D : Map Gene to Disease7756
BioCentury BCIQZNF207
ClinGenZNF207
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD7756
Chemical/Pharm GKB GenePA37578
Clinical trialZNF207
Miscellaneous
canSAR (ICR)ZNF207 (select the gene name)
Probes
Litterature
PubMed27 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF207
EVEXZNF207
GoPubMedZNF207
iHOPZNF207
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 14:42:27 CET 2017

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