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ZNF367 (zinc finger protein 367)

Identity

Alias_symbol (synonym)FLJ33970
Other aliasAFF29
CDC14B
ZFF29
HGNC (Hugo) ZNF367
LocusID (NCBI) 195828
Atlas_Id 55170
Location 9q22.32  [Link to chromosome band 9q22]
Location_base_pair Starts at 96385943 and ends at 96418387 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
ZNF367 (9q22.32) / CDC14B (9q22.32)

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)ZNF367   18320
Cards
Entrez_Gene (NCBI)ZNF367  195828  zinc finger protein 367
AliasesAFF29; CDC14B; ZFF29
GeneCards (Weizmann)ZNF367
Ensembl hg19 (Hinxton)ENSG00000165244 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000165244 [Gene_View]  chr9:96385943-96418387 [Contig_View]  ZNF367 [Vega]
ICGC DataPortalENSG00000165244
TCGA cBioPortalZNF367
AceView (NCBI)ZNF367
Genatlas (Paris)ZNF367
WikiGenes195828
SOURCE (Princeton)ZNF367
Genetics Home Reference (NIH)ZNF367
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF367  -     chr9:96385943-96418387 -  9q22.32   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF367  -     9q22.32   [Description]    (hg19-Feb_2009)
EnsemblZNF367 - 9q22.32 [CytoView hg19]  ZNF367 - 9q22.32 [CytoView hg38]
Mapping of homologs : NCBIZNF367 [Mapview hg19]  ZNF367 [Mapview hg38]
OMIM610160   
Gene and transcription
Genbank (Entrez)AK091289 AY554164 AY554165 BC126141 BK000211
RefSeq transcript (Entrez)NM_153695
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF367
Cluster EST : UnigeneHs.494557 [ NCBI ]
CGAP (NCI)Hs.494557
Alternative Splicing GalleryENSG00000165244
Gene ExpressionZNF367 [ NCBI-GEO ]   ZNF367 [ EBI - ARRAY_EXPRESS ]   ZNF367 [ SEEK ]   ZNF367 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF367 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)195828
GTEX Portal (Tissue expression)ZNF367
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ7RTV3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ7RTV3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ7RTV3
Splice isoforms : SwissVarQ7RTV3
PhosPhoSitePlusQ7RTV3
Domaine pattern : Prosite (Expaxy)ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)Znf_C2H2    Znf_C2H2-like    Znf_C2H2/integrase_DNA-bd   
Domain families : Pfam (Sanger)zf-C2H2_6 (PF13912)   
Domain families : Pfam (NCBI)pfam13912   
Domain families : Smart (EMBL)ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF367
DMDM Disease mutations195828
Blocks (Seattle)ZNF367
SuperfamilyQ7RTV3
Human Protein AtlasENSG00000165244
Peptide AtlasQ7RTV3
HPRD18330
IPIIPI00171725   IPI00845326   
Protein Interaction databases
DIP (DOE-UCLA)Q7RTV3
IntAct (EBI)Q7RTV3
FunCoupENSG00000165244
BioGRIDZNF367
STRING (EMBL)ZNF367
ZODIACZNF367
Ontologies - Pathways
QuickGOQ7RTV3
Ontology : AmiGODNA binding  transcription factor activity, sequence-specific DNA binding  nucleus  nucleoplasm  transcription, DNA-templated  regulation of transcription from RNA polymerase II promoter  metal ion binding  
Ontology : EGO-EBIDNA binding  transcription factor activity, sequence-specific DNA binding  nucleus  nucleoplasm  transcription, DNA-templated  regulation of transcription from RNA polymerase II promoter  metal ion binding  
NDEx NetworkZNF367
Atlas of Cancer Signalling NetworkZNF367
Wikipedia pathwaysZNF367
Orthology - Evolution
OrthoDB195828
GeneTree (enSembl)ENSG00000165244
Phylogenetic Trees/Animal Genes : TreeFamZNF367
HOVERGENQ7RTV3
HOGENOMQ7RTV3
Homologs : HomoloGeneZNF367
Homology/Alignments : Family Browser (UCSC)ZNF367
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF367 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF367
dbVarZNF367
ClinVarZNF367
1000_GenomesZNF367 
Exome Variant ServerZNF367
ExAC (Exome Aggregation Consortium)ZNF367 (select the gene name)
Genetic variants : HAPMAP195828
Genomic Variants (DGV)ZNF367 [DGVbeta]
DECIPHERZNF367 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF367 
Mutations
ICGC Data PortalZNF367 
TCGA Data PortalZNF367 
Broad Tumor PortalZNF367
OASIS PortalZNF367 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF367  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF367
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ZNF367
DgiDB (Drug Gene Interaction Database)ZNF367
DoCM (Curated mutations)ZNF367 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF367 (select a term)
intoGenZNF367
Cancer3DZNF367(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM610160   
Orphanet
MedgenZNF367
Genetic Testing Registry ZNF367
NextProtQ7RTV3 [Medical]
TSGene195828
GENETestsZNF367
Target ValidationZNF367
Huge Navigator ZNF367 [HugePedia]
snp3D : Map Gene to Disease195828
BioCentury BCIQZNF367
ClinGenZNF367
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD195828
Chemical/Pharm GKB GenePA38316
Clinical trialZNF367
Miscellaneous
canSAR (ICR)ZNF367 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF367
EVEXZNF367
GoPubMedZNF367
iHOPZNF367
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Aug 1 17:19:29 CEST 2017

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