Atlas of Genetics and Cytogenetics in Oncology and Haematology


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ZNF132 (zinc finger protein 132)

Identity

Alias_nameszinc finger protein 132 (clone pHZ-12)
Alias_symbol (synonym)pHZ-12
Other alias
HGNC (Hugo) ZNF132
LocusID (NCBI) 7691
Atlas_Id 52645
Location 19q13.43  [Link to chromosome band 19q13]
Location_base_pair Starts at 58432814 and ends at 58440222 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
ZNF132 (19q13.43) / ZNF584 (19q13.43)

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)ZNF132   12916
Cards
Entrez_Gene (NCBI)ZNF132  7691  zinc finger protein 132
AliasespHZ-12
GeneCards (Weizmann)ZNF132
Ensembl hg19 (Hinxton)ENSG00000131849 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000131849 [Gene_View]  ENSG00000131849 [Sequence]  chr19:58432814-58440222 [Contig_View]  ZNF132 [Vega]
ICGC DataPortalENSG00000131849
TCGA cBioPortalZNF132
AceView (NCBI)ZNF132
Genatlas (Paris)ZNF132
WikiGenes7691
SOURCE (Princeton)ZNF132
Genetics Home Reference (NIH)ZNF132
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF132  -     chr19:58432814-58440222 -  19q13.43   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF132  -     19q13.43   [Description]    (hg19-Feb_2009)
GoldenPathZNF132 - 19q13.43 [CytoView hg19]  ZNF132 - 19q13.43 [CytoView hg38]
ImmunoBaseENSG00000131849
Mapping of homologs : NCBIZNF132 [Mapview hg19]  ZNF132 [Mapview hg38]
OMIM604074   
Gene and transcription
Genbank (Entrez)AK057460 AK313895 BC109107 BC109108 BQ774411
RefSeq transcript (Entrez)NM_003433
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF132
Cluster EST : UnigeneHs.156169 [ NCBI ]
CGAP (NCI)Hs.156169
Alternative Splicing GalleryENSG00000131849
Gene ExpressionZNF132 [ NCBI-GEO ]   ZNF132 [ EBI - ARRAY_EXPRESS ]   ZNF132 [ SEEK ]   ZNF132 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF132 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)7691
GTEX Portal (Tissue expression)ZNF132
Human Protein AtlasENSG00000131849-ZNF132 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP52740   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP52740  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP52740
Splice isoforms : SwissVarP52740
PhosPhoSitePlusP52740
Domaine pattern : Prosite (Expaxy)KRAB (PS50805)    ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)KRAB    KRAB_dom_sf    Znf_C2H2_sf    Znf_C2H2_type   
Domain families : Pfam (Sanger)KRAB (PF01352)   
Domain families : Pfam (NCBI)pfam01352   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF132
DMDM Disease mutations7691
Blocks (Seattle)ZNF132
SuperfamilyP52740
Human Protein Atlas [tissue]ENSG00000131849-ZNF132 [tissue]
Peptide AtlasP52740
HPRD07240
IPIIPI00640627   IPI00004995   IPI00871983   
Protein Interaction databases
DIP (DOE-UCLA)P52740
IntAct (EBI)P52740
FunCoupENSG00000131849
BioGRIDZNF132
STRING (EMBL)ZNF132
ZODIACZNF132
Ontologies - Pathways
QuickGOP52740
Ontology : AmiGODNA-binding transcription factor activity, RNA polymerase II-specific  DNA binding  DNA-binding transcription factor activity  nucleus  regulation of transcription by RNA polymerase II  metal ion binding  
Ontology : EGO-EBIDNA-binding transcription factor activity, RNA polymerase II-specific  DNA binding  DNA-binding transcription factor activity  nucleus  regulation of transcription by RNA polymerase II  metal ion binding  
NDEx NetworkZNF132
Atlas of Cancer Signalling NetworkZNF132
Wikipedia pathwaysZNF132
Orthology - Evolution
OrthoDB7691
GeneTree (enSembl)ENSG00000131849
Phylogenetic Trees/Animal Genes : TreeFamZNF132
HOGENOMP52740
Homologs : HomoloGeneZNF132
Homology/Alignments : Family Browser (UCSC)ZNF132
Gene fusions - Rearrangements
Fusion : QuiverZNF132
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF132 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF132
dbVarZNF132
ClinVarZNF132
1000_GenomesZNF132 
Exome Variant ServerZNF132
ExAC (Exome Aggregation Consortium)ENSG00000131849
GNOMAD BrowserENSG00000131849
Varsome BrowserZNF132
Genetic variants : HAPMAP7691
Genomic Variants (DGV)ZNF132 [DGVbeta]
DECIPHERZNF132 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF132 
Mutations
ICGC Data PortalZNF132 
TCGA Data PortalZNF132 
Broad Tumor PortalZNF132
OASIS PortalZNF132 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF132  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DZNF132
Mutations and Diseases : HGMDZNF132
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 ZNF132
DgiDB (Drug Gene Interaction Database)ZNF132
DoCM (Curated mutations)ZNF132 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF132 (select a term)
intoGenZNF132
Cancer3DZNF132(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM604074   
Orphanet
DisGeNETZNF132
MedgenZNF132
Genetic Testing Registry ZNF132
NextProtP52740 [Medical]
TSGene7691
GENETestsZNF132
Target ValidationZNF132
Huge Navigator ZNF132 [HugePedia]
snp3D : Map Gene to Disease7691
BioCentury BCIQZNF132
ClinGenZNF132
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD7691
Chemical/Pharm GKB GenePA37505
Clinical trialZNF132
Miscellaneous
canSAR (ICR)ZNF132 (select the gene name)
DataMed IndexZNF132
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF132
EVEXZNF132
GoPubMedZNF132
iHOPZNF132
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 Nov 13 18:16:08 CET 2019

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