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ZNF503 (zinc finger protein 503)

Identity

Alias_symbol (synonym)FLJ45745
MGC2555
Nlz2
Other aliasNOLZ-1
NOLZ1
HGNC (Hugo) ZNF503
LocusID (NCBI) 84858
Atlas_Id 56337
Location 10q22.2  [Link to chromosome band 10q22]
Location_base_pair Starts at 75397830 and ends at 75401894 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
IGLON5 (19q13.41) / ZNF503 (10q22.2)ZNF503 (10q22.2) / IGLON5 (19q13.41)ZNF503 (10q22.2) / KIAA0895 (7p14.2)
ZNF503 (10q22.2) / ZNF503-AS2 (10q22.2)

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)ZNF503   23589
Cards
Entrez_Gene (NCBI)ZNF503  84858  zinc finger protein 503
AliasesNOLZ-1; NOLZ1; Nlz2
GeneCards (Weizmann)ZNF503
Ensembl hg19 (Hinxton)ENSG00000165655 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000165655 [Gene_View]  chr10:75397830-75401894 [Contig_View]  ZNF503 [Vega]
ICGC DataPortalENSG00000165655
TCGA cBioPortalZNF503
AceView (NCBI)ZNF503
Genatlas (Paris)ZNF503
WikiGenes84858
SOURCE (Princeton)ZNF503
Genetics Home Reference (NIH)ZNF503
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF503  -     chr10:75397830-75401894 -  10q22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF503  -     10q22.2   [Description]    (hg19-Feb_2009)
EnsemblZNF503 - 10q22.2 [CytoView hg19]  ZNF503 - 10q22.2 [CytoView hg38]
Mapping of homologs : NCBIZNF503 [Mapview hg19]  ZNF503 [Mapview hg38]
OMIM613902   
Gene and transcription
Genbank (Entrez)AI522172 AI701640 AK092897 AK127647 AK225851
RefSeq transcript (Entrez)NM_032772
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF503
Cluster EST : UnigeneHs.195710 [ NCBI ]
CGAP (NCI)Hs.195710
Alternative Splicing GalleryENSG00000165655
Gene ExpressionZNF503 [ NCBI-GEO ]   ZNF503 [ EBI - ARRAY_EXPRESS ]   ZNF503 [ SEEK ]   ZNF503 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF503 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)84858
GTEX Portal (Tissue expression)ZNF503
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96F45   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96F45  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96F45
Splice isoforms : SwissVarQ96F45
PhosPhoSitePlusQ96F45
Domaine pattern : Prosite (Expaxy)ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)Tscrpt_rep_NocA-like    Znf_C2H2    Znf_C2H2/integrase_DNA-bd   
Domain families : Pfam (Sanger)nlz1 (PF12402)   
Domain families : Pfam (NCBI)pfam12402   
Conserved Domain (NCBI)ZNF503
DMDM Disease mutations84858
Blocks (Seattle)ZNF503
SuperfamilyQ96F45
Human Protein AtlasENSG00000165655
Peptide AtlasQ96F45
HPRD15811
IPIIPI00304992   IPI00843984   IPI00386806   
Protein Interaction databases
DIP (DOE-UCLA)Q96F45
IntAct (EBI)Q96F45
FunCoupENSG00000165655
BioGRIDZNF503
STRING (EMBL)ZNF503
ZODIACZNF503
Ontologies - Pathways
QuickGOQ96F45
Ontology : AmiGOnucleic acid binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  negative regulation of cell proliferation  negative regulation of gene expression  metal ion binding  neural precursor cell proliferation  G1 to G0 transition involved in cell differentiation  
Ontology : EGO-EBInucleic acid binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  negative regulation of cell proliferation  negative regulation of gene expression  metal ion binding  neural precursor cell proliferation  G1 to G0 transition involved in cell differentiation  
NDEx NetworkZNF503
Atlas of Cancer Signalling NetworkZNF503
Wikipedia pathwaysZNF503
Orthology - Evolution
OrthoDB84858
GeneTree (enSembl)ENSG00000165655
Phylogenetic Trees/Animal Genes : TreeFamZNF503
HOVERGENQ96F45
HOGENOMQ96F45
Homologs : HomoloGeneZNF503
Homology/Alignments : Family Browser (UCSC)ZNF503
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF503 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF503
dbVarZNF503
ClinVarZNF503
1000_GenomesZNF503 
Exome Variant ServerZNF503
ExAC (Exome Aggregation Consortium)ZNF503 (select the gene name)
Genetic variants : HAPMAP84858
Genomic Variants (DGV)ZNF503 [DGVbeta]
DECIPHERZNF503 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF503 
Mutations
ICGC Data PortalZNF503 
TCGA Data PortalZNF503 
Broad Tumor PortalZNF503
OASIS PortalZNF503 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF503  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF503
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ZNF503
DgiDB (Drug Gene Interaction Database)ZNF503
DoCM (Curated mutations)ZNF503 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF503 (select a term)
intoGenZNF503
Cancer3DZNF503(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM613902   
Orphanet
MedgenZNF503
Genetic Testing Registry ZNF503
NextProtQ96F45 [Medical]
TSGene84858
GENETestsZNF503
Target ValidationZNF503
Huge Navigator ZNF503 [HugePedia]
snp3D : Map Gene to Disease84858
BioCentury BCIQZNF503
ClinGenZNF503
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD84858
Chemical/Pharm GKB GenePA134904334
Clinical trialZNF503
Miscellaneous
canSAR (ICR)ZNF503 (select the gene name)
Probes
Litterature
PubMed11 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF503
EVEXZNF503
GoPubMedZNF503
iHOPZNF503
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 13:03:50 CEST 2017

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