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MPV17L (MPV17 mitochondrial membrane protein-like)

Identity

Alias_symbol (synonym)FLJ39599
MLPH1
MLPH2
MPV17L1
Other aliasM-LPH
HGNC (Hugo) MPV17L
LocusID (NCBI) 255027
Atlas_Id 70399
Location 16p13.11  [Link to chromosome band 16p13]
Location_base_pair Starts at 15489611 and ends at 15503543 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
MPV17L (16p13.11) / XPO6 (16p11.2)

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)MPV17L   26827
Cards
Entrez_Gene (NCBI)MPV17L  255027  MPV17 mitochondrial membrane protein-like
AliasesM-LPH; MLPH1; MLPH2; MPV17L1
GeneCards (Weizmann)MPV17L
Ensembl hg19 (Hinxton) [Gene_View]  chr16:15489611-15503543 [Contig_View]  MPV17L [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr16:15489611-15503543 [Contig_View]  MPV17L [Vega]
TCGA cBioPortalMPV17L
AceView (NCBI)MPV17L
Genatlas (Paris)MPV17L
WikiGenes255027
SOURCE (Princeton)MPV17L
Genetics Home Reference (NIH)MPV17L
Genomic and cartography
GoldenPath hg19 (UCSC)MPV17L  -     chr16:15489611-15503543 +  16p13.11   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MPV17L  -     16p13.11   [Description]    (hg38-Dec_2013)
EnsemblMPV17L - 16p13.11 [CytoView hg19]  MPV17L - 16p13.11 [CytoView hg38]
Mapping of homologs : NCBIMPV17L [Mapview hg19]  MPV17L [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK096918 AK293380 BC061514 BM838624 DQ004255
RefSeq transcript (Entrez)NM_001128423 NM_173803
RefSeq genomic (Entrez)NC_000016 NC_018927 NT_010393 NT_187607 NW_004929400
Consensus coding sequences : CCDS (NCBI)MPV17L
Cluster EST : UnigeneHs.720673 [ NCBI ]
CGAP (NCI)Hs.720673
Gene ExpressionMPV17L [ NCBI-GEO ]   MPV17L [ EBI - ARRAY_EXPRESS ]   MPV17L [ SEEK ]   MPV17L [ MEM ]
Gene Expression Viewer (FireBrowse)MPV17L [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)255027
GTEX Portal (Tissue expression)MPV17L
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ2QL34   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ2QL34  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ2QL34
Splice isoforms : SwissVarQ2QL34
PhosPhoSitePlusQ2QL34
Domains : Interpro (EBI)Mpv17_PMP22   
Domain families : Pfam (Sanger)Mpv17_PMP22 (PF04117)   
Domain families : Pfam (NCBI)pfam04117   
Conserved Domain (NCBI)MPV17L
DMDM Disease mutations255027
Blocks (Seattle)MPV17L
SuperfamilyQ2QL34
Peptide AtlasQ2QL34
HPRD08803
IPIIPI00873917   IPI00167459   
Protein Interaction databases
DIP (DOE-UCLA)Q2QL34
IntAct (EBI)Q2QL34
BioGRIDMPV17L
STRING (EMBL)MPV17L
ZODIACMPV17L
Ontologies - Pathways
QuickGOQ2QL34
Ontology : AmiGOmolecular_function  receptor binding  peroxisome  peroxisomal membrane  negative regulation of hydrogen peroxide biosynthetic process  integral component of membrane  reactive oxygen species metabolic process  negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway  
Ontology : EGO-EBImolecular_function  receptor binding  peroxisome  peroxisomal membrane  negative regulation of hydrogen peroxide biosynthetic process  integral component of membrane  reactive oxygen species metabolic process  negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway  
Pathways : KEGGPeroxisome   
NDEx NetworkMPV17L
Atlas of Cancer Signalling NetworkMPV17L
Wikipedia pathwaysMPV17L
Orthology - Evolution
OrthoDB255027
Phylogenetic Trees/Animal Genes : TreeFamMPV17L
HOVERGENQ2QL34
HOGENOMQ2QL34
Homologs : HomoloGeneMPV17L
Homology/Alignments : Family Browser (UCSC)MPV17L
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMPV17L [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MPV17L
dbVarMPV17L
ClinVarMPV17L
1000_GenomesMPV17L 
Exome Variant ServerMPV17L
ExAC (Exome Aggregation Consortium)MPV17L (select the gene name)
Genetic variants : HAPMAP255027
Genomic Variants (DGV)MPV17L [DGVbeta]
DECIPHER (Syndromes)16:15489611-15503543  
CONAN: Copy Number AnalysisMPV17L 
Mutations
ICGC Data PortalMPV17L 
TCGA Data PortalMPV17L 
Broad Tumor PortalMPV17L
OASIS PortalMPV17L [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMPV17L  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMPV17L
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MPV17L
DgiDB (Drug Gene Interaction Database)MPV17L
DoCM (Curated mutations)MPV17L (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MPV17L (select a term)
intoGenMPV17L
Cancer3DMPV17L(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMPV17L
Genetic Testing Registry MPV17L
NextProtQ2QL34 [Medical]
TSGene255027
GENETestsMPV17L
Huge Navigator MPV17L [HugePedia]
snp3D : Map Gene to Disease255027
BioCentury BCIQMPV17L
ClinGenMPV17L
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD255027
Chemical/Pharm GKB GenePA145007960
Clinical trialMPV17L
Miscellaneous
canSAR (ICR)MPV17L (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMPV17L
EVEXMPV17L
GoPubMedMPV17L
iHOPMPV17L
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 12:33:32 CET 2017

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