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DNLZ (DNL-type zinc finger)

Identity

Alias (NCBI)C9orf151
HEP
HEP1
TIMM15
ZIM17
bA413M3.2
HGNC (Hugo) DNLZ
HGNC Alias symbRP11-413M3.2
ZIM17
bA413M3.2
TIMM15
HEP
HGNC Alias nametranslocase of inner mitochondrial membrane 15 homolog (yeast)
 HSP70 escort protein
HGNC Previous nameC9orf151
HGNC Previous namechromosome 9 open reading frame 151
LocusID (NCBI) 728489
Atlas_Id 62578
Location 9q34.3  [Link to chromosome band 9q34]
Location_base_pair Starts at 136359483 and ends at 136363744 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)

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)DNLZ   33879
Cards
Entrez_Gene (NCBI)DNLZ    DNL-type zinc finger
AliasesC9orf151; HEP; HEP1; TIMM15; 
ZIM17; bA413M3.2
GeneCards (Weizmann)DNLZ
Ensembl hg19 (Hinxton)ENSG00000213221 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000213221 [Gene_View]  ENSG00000213221 [Sequence]  chr9:136359483-136363744 [Contig_View]  DNLZ [Vega]
ICGC DataPortalENSG00000213221
TCGA cBioPortalDNLZ
AceView (NCBI)DNLZ
Genatlas (Paris)DNLZ
SOURCE (Princeton)DNLZ
Genetics Home Reference (NIH)DNLZ
Genomic and cartography
GoldenPath hg38 (UCSC)DNLZ  -     chr9:136359483-136363744 -  9q34.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)DNLZ  -     9q34.3   [Description]    (hg19-Feb_2009)
GoldenPathDNLZ - 9q34.3 [CytoView hg19]  DNLZ - 9q34.3 [CytoView hg38]
ImmunoBaseENSG00000213221
Genome Data Viewer NCBIDNLZ [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AI435052 AI696701 BC146915 BC146924 BC171835
RefSeq transcript (Entrez)NM_001080849
Consensus coding sequences : CCDS (NCBI)DNLZ
Gene ExpressionDNLZ [ NCBI-GEO ]   DNLZ [ EBI - ARRAY_EXPRESS ]   DNLZ [ SEEK ]   DNLZ [ MEM ]
Gene Expression Viewer (FireBrowse)DNLZ [ Firebrowse - Broad ]
GenevisibleExpression of DNLZ in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)728489
GTEX Portal (Tissue expression)DNLZ
Human Protein AtlasENSG00000213221-DNLZ [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5SXM8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5SXM8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5SXM8
PhosPhoSitePlusQ5SXM8
Domaine pattern : Prosite (Expaxy)ZF_DNL (PS51501)   
Domains : Interpro (EBI)Mt_import_TIM15    Znf_DNL-typ   
Domain families : Pfam (Sanger)zf-DNL (PF05180)   
Domain families : Pfam (NCBI)pfam05180   
Conserved Domain (NCBI)DNLZ
SuperfamilyQ5SXM8
AlphaFold pdb e-kbQ5SXM8   
Human Protein Atlas [tissue]ENSG00000213221-DNLZ [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q5SXM8
IntAct (EBI)Q5SXM8
BioGRIDDNLZ
STRING (EMBL)DNLZ
ZODIACDNLZ
Ontologies - Pathways
QuickGOQ5SXM8
Ontology : AmiGOnucleoplasm  mitochondrion  mitochondrion  protein folding  zinc ion binding  protein import into mitochondrial matrix  protein stabilization  chaperone binding  
Ontology : EGO-EBInucleoplasm  mitochondrion  mitochondrion  protein folding  zinc ion binding  protein import into mitochondrial matrix  protein stabilization  chaperone binding  
NDEx NetworkDNLZ
Atlas of Cancer Signalling NetworkDNLZ
Wikipedia pathwaysDNLZ
Orthology - Evolution
OrthoDB728489
GeneTree (enSembl)ENSG00000213221
Phylogenetic Trees/Animal Genes : TreeFamDNLZ
Homologs : HomoloGeneDNLZ
Homology/Alignments : Family Browser (UCSC)DNLZ
Gene fusions - Rearrangements
Fusion : QuiverDNLZ
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerDNLZ [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DNLZ
dbVarDNLZ
ClinVarDNLZ
MonarchDNLZ
1000_GenomesDNLZ 
Exome Variant ServerDNLZ
GNOMAD BrowserENSG00000213221
Varsome BrowserDNLZ
ACMGDNLZ variants
VarityQ5SXM8
Genomic Variants (DGV)DNLZ [DGVbeta]
DECIPHERDNLZ [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisDNLZ 
Mutations
ICGC Data PortalDNLZ 
TCGA Data PortalDNLZ 
Broad Tumor PortalDNLZ
OASIS PortalDNLZ [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICDNLZ  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DDNLZ
Mutations and Diseases : HGMDDNLZ
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaDNLZ
DgiDB (Drug Gene Interaction Database)DNLZ
DoCM (Curated mutations)DNLZ
CIViC (Clinical Interpretations of Variants in Cancer)DNLZ
Cancer3DDNLZ
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETDNLZ
MedgenDNLZ
Genetic Testing Registry DNLZ
NextProtQ5SXM8 [Medical]
GENETestsDNLZ
Target ValidationDNLZ
Huge Navigator DNLZ [HugePedia]
ClinGenDNLZ
Clinical trials, drugs, therapy
MyCancerGenomeDNLZ
Protein Interactions : CTDDNLZ
Pharm GKB GenePA162384018
PharosQ5SXM8
Clinical trialDNLZ
Miscellaneous
canSAR (ICR)DNLZ
HarmonizomeDNLZ
DataMed IndexDNLZ
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXDNLZ
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:48:13 CEST 2021

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