Atlas of Genetics and Cytogenetics in Oncology and Haematology


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ZNF737 (zinc finger protein 737)

Identity

Alias_symbol (synonym)ZNF102
Other alias
HGNC (Hugo) ZNF737
LocusID (NCBI) 100129842
Atlas_Id 76372
Location 19p12  [Link to chromosome band 19p12]
Location_base_pair Starts at 20537992 and ends at 20565820 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)ZNF737   32468
Cards
Entrez_Gene (NCBI)ZNF737  100129842  zinc finger protein 737
AliasesZNF102
GeneCards (Weizmann)ZNF737
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr19:20537992-20565820 [Contig_View]  ZNF737 [Vega]
TCGA cBioPortalZNF737
AceView (NCBI)ZNF737
Genatlas (Paris)ZNF737
WikiGenes100129842
SOURCE (Princeton)ZNF737
Genetics Home Reference (NIH)ZNF737
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF737  -     chr19:20537992-20565820 -  19p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF737  -     19p12   [Description]    (hg19-Feb_2009)
EnsemblZNF737 - 19p12 [CytoView hg19]  ZNF737 - 19p12 [CytoView hg38]
Mapping of homologs : NCBIZNF737 [Mapview hg19]  ZNF737 [Mapview hg38]
OMIM603984   
Gene and transcription
Genbank (Entrez)AI857360 DA043454
RefSeq transcript (Entrez)NM_001159293
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF737
Cluster EST : UnigeneHs.515696 [ NCBI ]
CGAP (NCI)Hs.515696
Gene ExpressionZNF737 [ NCBI-GEO ]   ZNF737 [ EBI - ARRAY_EXPRESS ]   ZNF737 [ SEEK ]   ZNF737 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF737 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100129842
GTEX Portal (Tissue expression)ZNF737
Protein : pattern, domain, 3D structure
UniProt/SwissProtO75373   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO75373  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO75373
Splice isoforms : SwissVarO75373
PhosPhoSitePlusO75373
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)ZNF737
DMDM Disease mutations100129842
Blocks (Seattle)ZNF737
SuperfamilyO75373
Peptide AtlasO75373
IPIIPI00643418   
Protein Interaction databases
DIP (DOE-UCLA)O75373
IntAct (EBI)O75373
BioGRIDZNF737
STRING (EMBL)ZNF737
ZODIACZNF737
Ontologies - Pathways
QuickGOO75373
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 NetworkZNF737
Atlas of Cancer Signalling NetworkZNF737
Wikipedia pathwaysZNF737
Orthology - Evolution
OrthoDB100129842
Phylogenetic Trees/Animal Genes : TreeFamZNF737
HOVERGENO75373
HOGENOMO75373
Homologs : HomoloGeneZNF737
Homology/Alignments : Family Browser (UCSC)ZNF737
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF737 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF737
dbVarZNF737
ClinVarZNF737
1000_GenomesZNF737 
Exome Variant ServerZNF737
ExAC (Exome Aggregation Consortium)ZNF737 (select the gene name)
Genetic variants : HAPMAP100129842
Genomic Variants (DGV)ZNF737 [DGVbeta]
DECIPHERZNF737 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF737 
Mutations
ICGC Data PortalZNF737 
TCGA Data PortalZNF737 
Broad Tumor PortalZNF737
OASIS PortalZNF737 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF737  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF737
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 ZNF737
DgiDB (Drug Gene Interaction Database)ZNF737
DoCM (Curated mutations)ZNF737 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF737 (select a term)
intoGenZNF737
Cancer3DZNF737(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM603984   
Orphanet
MedgenZNF737
Genetic Testing Registry ZNF737
NextProtO75373 [Medical]
TSGene100129842
GENETestsZNF737
Huge Navigator ZNF737 [HugePedia]
snp3D : Map Gene to Disease100129842
BioCentury BCIQZNF737
ClinGenZNF737
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100129842
Chemical/Pharm GKB GenePA162410269
Clinical trialZNF737
Miscellaneous
canSAR (ICR)ZNF737 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF737
EVEXZNF737
GoPubMedZNF737
iHOPZNF737
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri May 19 12:03:45 CEST 2017

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