Atlas of Genetics and Cytogenetics in Oncology and Haematology

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

Taking over the Atlas
Dear Colleagues,
The Atlas, once more, is in great danger, and I will have to proceed to a collective economic lay-off of all the team involved in the Atlas before the begining of April 2015 (a foundation having suddenly withdrawn its commitment to support the Atlas). I ask you herein if any Scientific Society (a Society of Cytogenetics, of Clinical Genetics, of Hematology, or a Cancer Society, or any other...), any University and/or Hospital, any Charity, or any database would be interested in taking over the Atlas, in whole or in part. If taking charge of the whole lot is too big, a consortium of various actors could be the solution (I am myself trying to find partners). Could you please spread the information, contact the relevant authorities, and find partners.
Survival of the Atlas will be critically dependant upon your ability to find solutions (and urgently!).
Kind regards.
Jean-Loup Huret
Donations are also welcome

Donate (in Euros)

Donate (in US Dollars)

ZNF365 (zinc finger protein 365)


Other namesSu48
HGNC (Hugo) ZNF365
LocusID (NCBI) 22891
Location 10q21.2
Location_base_pair Starts at 64133916 and ends at 64162217 bp from pter ( according to hg19-Feb_2009)

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

External links

HGNC (Hugo)ZNF365   18194
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
AceView (NCBI)ZNF365
Genatlas (Paris)ZNF365
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)AC_000142 NC_000010 NC_018921 NG_021209 NT_030059 NW_001837986 NW_004929376
Consensus coding sequences : CCDS (NCBI)ZNF365
Cluster EST : UnigeneHs.22653 [ NCBI ]
CGAP (NCI)Hs.22653
Alternative Splicing : Fast-db (Paris)GSHG0003399
Alternative Splicing GalleryENSG00000138311
Gene ExpressionZNF365 [ NCBI-GEO ]     ZNF365 [ SEEK ]   ZNF365 [ MEM ]
SOURCE (Princeton)Expression in : [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ70YC5 (Uniprot)
NextProtQ70YC5  [Medical]
With graphics : InterProQ70YC5
Splice isoforms : SwissVarQ70YC5 (Swissvar)
Domains : Interpro (EBI)Znf_C2H2-like   
Related proteins : CluSTrQ70YC5
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Domain families : Smart (EMBL)ZnF_C2H2 (SM00355)  
DMDM Disease mutations22891
Blocks (Seattle)Q70YC5
Human Protein AtlasENSG00000138311
Peptide AtlasQ70YC5
IPIIPI00399362   IPI00007274   IPI00418945   IPI00399361   IPI00657879   IPI00658173   IPI00645190   IPI00790285   IPI00927818   
Protein Interaction databases
IntAct (EBI)Q70YC5
Ontologies - Pathways
Ontology : AmiGOprotein binding  cytoplasm  microtubule organizing center  
Ontology : EGO-EBIprotein binding  cytoplasm  microtubule organizing center  
Protein Interaction DatabaseZNF365
DoCM (Curated mutations)ZNF365
Wikipedia pathwaysZNF365
Gene fusion - rearrangements
Polymorphisms : SNP, variants
NCBI Variation ViewerZNF365 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF365
Exome Variant ServerZNF365
SNP (GeneSNP Utah)ZNF365
SNP : HGBaseZNF365
Genetic variants : HAPMAPZNF365
Genomic Variants (DGV)ZNF365 [DGVbeta]
ICGC Data PortalENSG00000138311 
Somatic Mutations in Cancer : COSMICZNF365 
CONAN: Copy Number AnalysisZNF365 
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
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] 
DECIPHER (Syndromes)10:64133916-64162217
Mutations and Diseases : HGMDZNF365
OMIM605990    607818   
NextProtQ70YC5 [Medical]
Disease Genetic AssociationZNF365
Huge Navigator ZNF365 [HugePedia]  ZNF365 [HugeCancerGEM]
snp3D : Map Gene to Disease22891
DGIdb (Drug Gene Interaction db)ZNF365
General knowledge
Homologs : HomoloGeneZNF365
Homology/Alignments : Family Browser (UCSC)ZNF365
Phylogenetic Trees/Animal Genes : TreeFamZNF365
Chemical/Protein Interactions : CTD22891
Chemical/Pharm GKB GenePA134873576
Clinical trialZNF365
Cancer Resource (Charite)ENSG00000138311
Other databases
PubMed37 Pubmed reference(s) in Entrez
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI


Written09-2002Dessen P, Le Minor S
Updated12-2014Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Sat Feb 14 19:29:54 CET 2015

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us