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ZNF134 (zinc finger protein 134)

Identity

Alias_nameszinc finger protein 134 (clone pHZ-15)
Alias_symbol (synonym)pHZ-15
Other alias
HGNC (Hugo) ZNF134
LocusID (NCBI) 7693
Atlas_Id 46962
Location 19q13.43  [Link to chromosome band 19q13]
Location_base_pair Starts at 58125830 and ends at 58133636 bp from pter ( according to hg19-Feb_2009)

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)ZNF134   12918
Cards
Entrez_Gene (NCBI)ZNF134  7693  zinc finger protein 134
AliasespHZ-15
GeneCards (Weizmann)ZNF134
Ensembl hg19 (Hinxton)ENSG00000213762 [Gene_View]  chr19:58125830-58133636 [Contig_View]  ZNF134 [Vega]
Ensembl hg38 (Hinxton)ENSG00000213762 [Gene_View]  chr19:58125830-58133636 [Contig_View]  ZNF134 [Vega]
ICGC DataPortalENSG00000213762
TCGA cBioPortalZNF134
AceView (NCBI)ZNF134
Genatlas (Paris)ZNF134
WikiGenes7693
SOURCE (Princeton)ZNF134
Genetics Home Reference (NIH)ZNF134
Genomic and cartography
GoldenPath hg19 (UCSC)ZNF134  -     chr19:58125830-58133636 +  19q13.43   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ZNF134  -     19q13.43   [Description]    (hg38-Dec_2013)
EnsemblZNF134 - 19q13.43 [CytoView hg19]  ZNF134 - 19q13.43 [CytoView hg38]
Mapping of homologs : NCBIZNF134 [Mapview hg19]  ZNF134 [Mapview hg38]
OMIM604076   
Gene and transcription
Genbank (Entrez)AK291763 BC011646 BC021280 BC042636 BC112294
RefSeq transcript (Entrez)NM_003435
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011109 NW_004929415
Consensus coding sequences : CCDS (NCBI)ZNF134
Cluster EST : UnigeneHs.469694 [ NCBI ]
CGAP (NCI)Hs.469694
Alternative Splicing GalleryENSG00000213762
Gene ExpressionZNF134 [ NCBI-GEO ]   ZNF134 [ EBI - ARRAY_EXPRESS ]   ZNF134 [ SEEK ]   ZNF134 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF134 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)7693
GTEX Portal (Tissue expression)ZNF134
Protein : pattern, domain, 3D structure
UniProt/SwissProtP52741   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP52741  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP52741
Splice isoforms : SwissVarP52741
PhosPhoSitePlusP52741
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 (PF00096)   
Domain families : Pfam (NCBI)pfam00096   
Domain families : Smart (EMBL)ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF134
DMDM Disease mutations7693
Blocks (Seattle)ZNF134
SuperfamilyP52741
Human Protein AtlasENSG00000213762
Peptide AtlasP52741
HPRD07241
IPIIPI00914633   IPI00472832   IPI01018672   IPI00952728   
Protein Interaction databases
DIP (DOE-UCLA)P52741
IntAct (EBI)P52741
FunCoupENSG00000213762
BioGRIDZNF134
STRING (EMBL)ZNF134
ZODIACZNF134
Ontologies - Pathways
QuickGOP52741
Ontology : AmiGODNA binding  transcription factor activity, sequence-specific DNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
Ontology : EGO-EBIDNA binding  transcription factor activity, sequence-specific DNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
NDEx NetworkZNF134
Atlas of Cancer Signalling NetworkZNF134
Wikipedia pathwaysZNF134
Orthology - Evolution
OrthoDB7693
GeneTree (enSembl)ENSG00000213762
Phylogenetic Trees/Animal Genes : TreeFamZNF134
HOVERGENP52741
HOGENOMP52741
Homologs : HomoloGeneZNF134
Homology/Alignments : Family Browser (UCSC)ZNF134
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF134 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF134
dbVarZNF134
ClinVarZNF134
1000_GenomesZNF134 
Exome Variant ServerZNF134
ExAC (Exome Aggregation Consortium)ZNF134 (select the gene name)
Genetic variants : HAPMAP7693
Genomic Variants (DGV)ZNF134 [DGVbeta]
DECIPHER (Syndromes)19:58125830-58133636  ENSG00000213762
CONAN: Copy Number AnalysisZNF134 
Mutations
ICGC Data PortalZNF134 
TCGA Data PortalZNF134 
Broad Tumor PortalZNF134
OASIS PortalZNF134 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF134  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF134
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ZNF134
DgiDB (Drug Gene Interaction Database)ZNF134
DoCM (Curated mutations)ZNF134 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF134 (select a term)
intoGenZNF134
Cancer3DZNF134(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM604076   
Orphanet
MedgenZNF134
Genetic Testing Registry ZNF134
NextProtP52741 [Medical]
TSGene7693
GENETestsZNF134
Huge Navigator ZNF134 [HugePedia]
snp3D : Map Gene to Disease7693
BioCentury BCIQZNF134
ClinGenZNF134
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD7693
Chemical/Pharm GKB GenePA37506
Clinical trialZNF134
Miscellaneous
canSAR (ICR)ZNF134 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF134
EVEXZNF134
GoPubMedZNF134
iHOPZNF134
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 13:34:56 CET 2017

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