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ZNF365 (zinc finger protein 365)

Identity

Other namesSu48
UAN
ZNF365D
HGNC (Hugo) ZNF365
LocusID (NCBI) 22891
Atlas_Id 52863
Location 10q21.2
Location_base_pair Starts at 64133916 and ends at 64162217 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
FAM13C (10q21.1) / ZNF365 (10q21.2)FAM13C 10q21.1 / ZNF365 10q21.2

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)ZNF365   18194
Cards
Entrez_Gene (NCBI)ZNF365  22891  zinc finger protein 365
GeneCards (Weizmann)ZNF365
Ensembl hg19 (Hinxton)ENSG00000138311 [Gene_View]  chr10:64133916-64162217 [Contig_View]  ZNF365 [Vega]
Ensembl hg38 (Hinxton)ENSG00000138311 [Gene_View]  chr10:64133916-64162217 [Contig_View]  ZNF365 [Vega]
ICGC DataPortalENSG00000138311
TCGA cBioPortalZNF365
AceView (NCBI)ZNF365
Genatlas (Paris)ZNF365
WikiGenes22891
SOURCE (Princeton)ZNF365
Genomic and cartography
GoldenPath hg19 (UCSC)ZNF365  -     chr10:64133916-64162217 +  10q21.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ZNF365  -     10q21.2   [Description]    (hg38-Dec_2013)
EnsemblZNF365 - 10q21.2 [CytoView hg19]  ZNF365 - 10q21.2 [CytoView hg38]
Mapping of homologs : NCBIZNF365 [Mapview hg19]  ZNF365 [Mapview hg38]
OMIM605990   607818   
Gene and transcription
Genbank (Entrez)AB020651 AJ505147 AJ505148 AJ505149 AJ505150
RefSeq transcript (Entrez)NM_014951 NM_199450 NM_199451 NM_199452
RefSeq genomic (Entrez)NC_000010 NC_018921 NG_021209 NT_030059 NW_004929376
Consensus coding sequences : CCDS (NCBI)ZNF365
Cluster EST : UnigeneHs.22653 [ NCBI ]
CGAP (NCI)Hs.22653
Alternative Splicing GalleryENSG00000138311
Gene ExpressionZNF365 [ NCBI-GEO ]   ZNF365 [ EBI - ARRAY_EXPRESS ]   ZNF365 [ SEEK ]   ZNF365 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF365 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)22891
GTEX Portal (Tissue expression)ZNF365
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ70YC5 (Uniprot)
NextProtQ70YC5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ70YC5
Splice isoforms : SwissVarQ70YC5 (Swissvar)
PhosPhoSitePlusQ70YC5
Domains : Interpro (EBI)Znf_C2H2-like   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Domain families : Smart (EMBL)ZnF_C2H2 (SM00355)  
DMDM Disease mutations22891
Blocks (Seattle)ZNF365
SuperfamilyQ70YC5
Human Protein AtlasENSG00000138311
Peptide AtlasQ70YC5
HPRD06380
IPIIPI00399362   IPI00007274   IPI00418945   IPI00399361   IPI00657879   IPI00658173   IPI00645190   IPI00790285   IPI00927818   
Protein Interaction databases
DIP (DOE-UCLA)Q70YC5
IntAct (EBI)Q70YC5
FunCoupENSG00000138311
BioGRIDZNF365
STRING (EMBL)ZNF365
ZODIACZNF365
Ontologies - Pathways
QuickGOQ70YC5
Ontology : AmiGOmitotic cytokinesis  gamma-tubulin complex  protein binding  cytoplasm  centrosome  microtubule organizing center  gamma-tubulin complex localization  protein homodimerization activity  
Ontology : EGO-EBImitotic cytokinesis  gamma-tubulin complex  protein binding  cytoplasm  centrosome  microtubule organizing center  gamma-tubulin complex localization  protein homodimerization activity  
NDEx Network
Atlas of Cancer Signalling NetworkZNF365
Wikipedia pathwaysZNF365
Orthology - Evolution
OrthoDB22891
GeneTree (enSembl)ENSG00000138311
Phylogenetic Trees/Animal Genes : TreeFamZNF365
Homologs : HomoloGeneZNF365
Homology/Alignments : Family Browser (UCSC)ZNF365
Gene fusions - Rearrangements
Fusion: TCGAFAM13C 10q21.1 ZNF365 10q21.2 BLCA
Polymorphisms : SNP, variants
NCBI Variation ViewerZNF365 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF365
dbVarZNF365
ClinVarZNF365
1000_GenomesZNF365 
Exome Variant ServerZNF365
ExAC (Exome Aggregation Consortium)ZNF365 (select the gene name)
Genetic variants : HAPMAP22891
Genomic Variants (DGV)ZNF365 [DGVbeta]
Mutations
ICGC Data PortalZNF365 
TCGA Data PortalZNF365 
Broad Tumor PortalZNF365
OASIS PortalZNF365 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF365 
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 ZNF365
DgiDB (Drug Gene Interaction Database)ZNF365
DoCM (Curated mutations)ZNF365 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF365 (select a term)
intoGenZNF365
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] 
Diseases
DECIPHER (Syndromes)10:64133916-64162217  ENSG00000138311
CONAN: Copy Number AnalysisZNF365 
Mutations and Diseases : HGMDZNF365
OMIM605990    607818   
MedgenZNF365
Genetic Testing Registry ZNF365
NextProtQ70YC5 [Medical]
TSGene22891
GENETestsZNF365
Huge Navigator ZNF365 [HugePedia]
snp3D : Map Gene to Disease22891
BioCentury BCIQZNF365
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD22891
Chemical/Pharm GKB GenePA134873576
Clinical trialZNF365
Miscellaneous
canSAR (ICR)ZNF365 (select the gene name)
Probes
Litterature
PubMed45 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF365
EVEXZNF365
GoPubMedZNF365
iHOPZNF365
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sun May 8 19:12:19 CEST 2016

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