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ZNF137P (zinc finger protein 137, pseudogene)

Identity

Alias_namesZNF137
zinc finger protein 137 (clone pHZ-30)
zinc finger protein 137
zinc finger protein 137 (pseudogene)
Alias_symbol (synonym)pHZ-30
Other alias
HGNC (Hugo) ZNF137P
LocusID (NCBI) 7696
Atlas_Id 75995
Location 19q13.41  [Link to chromosome band 19q13]
Location_base_pair Starts at 52596684 and ends at 52598539 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)ZNF137P   12921
Cards
Entrez_Gene (NCBI)ZNF137P  7696  zinc finger protein 137, pseudogene
AliasesZNF137; pHZ-30
GeneCards (Weizmann)ZNF137P
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr19:52596684-52598539 [Contig_View]  ZNF137P [Vega]
TCGA cBioPortalZNF137P
AceView (NCBI)ZNF137P
Genatlas (Paris)ZNF137P
WikiGenes7696
SOURCE (Princeton)ZNF137P
Genetics Home Reference (NIH)ZNF137P
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF137P  -     chr19:52596684-52598539 +  19q13.41   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF137P  -     19q13.41   [Description]    (hg19-Feb_2009)
EnsemblZNF137P - 19q13.41 [CytoView hg19]  ZNF137P - 19q13.41 [CytoView hg38]
Mapping of homologs : NCBIZNF137P [Mapview hg19]  ZNF137P [Mapview hg38]
OMIM604079   
Gene and transcription
Genbank (Entrez)BC110455 BC110456 BM988340 BQ893730 U09414
RefSeq transcript (Entrez)NM_003438
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF137P
Cluster EST : UnigeneHs.373648 [ NCBI ]
CGAP (NCI)Hs.373648
Gene ExpressionZNF137P [ NCBI-GEO ]   ZNF137P [ EBI - ARRAY_EXPRESS ]   ZNF137P [ SEEK ]   ZNF137P [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF137P [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)7696
GTEX Portal (Tissue expression)ZNF137P
Protein : pattern, domain, 3D structure
UniProt/SwissProtP52743   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP52743  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP52743
Splice isoforms : SwissVarP52743
PhosPhoSitePlusP52743
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)ZNF137P
DMDM Disease mutations7696
Blocks (Seattle)ZNF137P
SuperfamilyP52743
Peptide AtlasP52743
HPRD07243
IPIIPI00005001   
Protein Interaction databases
DIP (DOE-UCLA)P52743
IntAct (EBI)P52743
BioGRIDZNF137P
STRING (EMBL)ZNF137P
ZODIACZNF137P
Ontologies - Pathways
QuickGOP52743
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkZNF137P
Atlas of Cancer Signalling NetworkZNF137P
Wikipedia pathwaysZNF137P
Orthology - Evolution
OrthoDB7696
Phylogenetic Trees/Animal Genes : TreeFamZNF137P
HOVERGENP52743
HOGENOMP52743
Homologs : HomoloGeneZNF137P
Homology/Alignments : Family Browser (UCSC)ZNF137P
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF137P [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF137P
dbVarZNF137P
ClinVarZNF137P
1000_GenomesZNF137P 
Exome Variant ServerZNF137P
ExAC (Exome Aggregation Consortium)ZNF137P (select the gene name)
Genetic variants : HAPMAP7696
Genomic Variants (DGV)ZNF137P [DGVbeta]
DECIPHERZNF137P [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF137P 
Mutations
ICGC Data PortalZNF137P 
TCGA Data PortalZNF137P 
Broad Tumor PortalZNF137P
OASIS PortalZNF137P [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDZNF137P
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 ZNF137P
DgiDB (Drug Gene Interaction Database)ZNF137P
DoCM (Curated mutations)ZNF137P (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF137P (select a term)
intoGenZNF137P
Cancer3DZNF137P(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM604079   
Orphanet
MedgenZNF137P
Genetic Testing Registry ZNF137P
NextProtP52743 [Medical]
TSGene7696
GENETestsZNF137P
Target ValidationZNF137P
Huge Navigator ZNF137P [HugePedia]
snp3D : Map Gene to Disease7696
BioCentury BCIQZNF137P
ClinGenZNF137P
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD7696
Chemical/Pharm GKB GenePA37509
Clinical trialZNF137P
Miscellaneous
canSAR (ICR)ZNF137P (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF137P
EVEXZNF137P
GoPubMedZNF137P
iHOPZNF137P
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:44:25 CEST 2017

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