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ZNF735 (zinc finger protein 735)

Identity

Alias_namesZNF735P
zinc finger protein 735, pseudogene
Other alias
HGNC (Hugo) ZNF735
LocusID (NCBI) 730291
Atlas_Id 76370
Location 7q11.21  [Link to chromosome band 7q11]
Location_base_pair Starts at 64207203 and ends at 64220290 bp from pter ( according to hg38-Dec_2013)

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)ZNF735   32466
Cards
Entrez_Gene (NCBI)ZNF735  730291  zinc finger protein 735
AliasesZNF735P
GeneCards (Weizmann)ZNF735
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr7:64207203-64220290 [Contig_View]  ZNF735 [Vega]
TCGA cBioPortalZNF735
AceView (NCBI)ZNF735
Genatlas (Paris)ZNF735
WikiGenes730291
SOURCE (Princeton)ZNF735
Genetics Home Reference (NIH)ZNF735
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF735  -     chr7:64207203-64220290 +  7q11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF735  -     7q11.21   [Description]    (hg19-Feb_2009)
EnsemblZNF735 - 7q11.21 [CytoView hg19]  ZNF735 - 7q11.21 [CytoView hg38]
Mapping of homologs : NCBIZNF735 [Mapview hg19]  ZNF735 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001159524
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF735
Cluster EST : UnigeneHs.723116 [ NCBI ]
CGAP (NCI)Hs.723116
Gene ExpressionZNF735 [ NCBI-GEO ]   ZNF735 [ EBI - ARRAY_EXPRESS ]   ZNF735 [ SEEK ]   ZNF735 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF735 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)730291
GTEX Portal (Tissue expression)ZNF735
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0CB33   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0CB33  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0CB33
Splice isoforms : SwissVarP0CB33
PhosPhoSitePlusP0CB33
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)    zf-C2H2 (PF00096)    zf-C2H2_6 (PF13912)   
Domain families : Pfam (NCBI)pfam01352    pfam00096    pfam13912   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF735
DMDM Disease mutations730291
Blocks (Seattle)ZNF735
SuperfamilyP0CB33
Peptide AtlasP0CB33
IPIIPI00887168   
Protein Interaction databases
DIP (DOE-UCLA)P0CB33
IntAct (EBI)P0CB33
BioGRIDZNF735
STRING (EMBL)ZNF735
ZODIACZNF735
Ontologies - Pathways
QuickGOP0CB33
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 NetworkZNF735
Atlas of Cancer Signalling NetworkZNF735
Wikipedia pathwaysZNF735
Orthology - Evolution
OrthoDB730291
Phylogenetic Trees/Animal Genes : TreeFamZNF735
HOVERGENP0CB33
HOGENOMP0CB33
Homologs : HomoloGeneZNF735
Homology/Alignments : Family Browser (UCSC)ZNF735
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF735 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF735
dbVarZNF735
ClinVarZNF735
1000_GenomesZNF735 
Exome Variant ServerZNF735
ExAC (Exome Aggregation Consortium)ZNF735 (select the gene name)
Genetic variants : HAPMAP730291
Genomic Variants (DGV)ZNF735 [DGVbeta]
DECIPHERZNF735 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF735 
Mutations
ICGC Data PortalZNF735 
TCGA Data PortalZNF735 
Broad Tumor PortalZNF735
OASIS PortalZNF735 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDZNF735
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 ZNF735
DgiDB (Drug Gene Interaction Database)ZNF735
DoCM (Curated mutations)ZNF735 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF735 (select a term)
intoGenZNF735
Cancer3DZNF735(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF735
Genetic Testing Registry ZNF735
NextProtP0CB33 [Medical]
TSGene730291
GENETestsZNF735
Target ValidationZNF735
Huge Navigator ZNF735 [HugePedia]
snp3D : Map Gene to Disease730291
BioCentury BCIQZNF735
ClinGenZNF735
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD730291
Chemical/Pharm GKB GenePA162410268
Clinical trialZNF735
Miscellaneous
canSAR (ICR)ZNF735 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF735
EVEXZNF735
GoPubMedZNF735
iHOPZNF735
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 : Wed May 31 15:51:12 CEST 2017

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