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MTRNR2L7 (MT-RNR2 like 7)

Identity

Alias (NCBI)HN7
HGNC (Hugo) MTRNR2L7
HGNC Alias namehumanin-like 7
LocusID (NCBI) 100288485
Atlas_Id 70573
Location 10p11.21  [Link to chromosome band 10p11]
Location_base_pair Starts at 37601438 and ends at 37602931 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)MTRNR2L7   37164
Cards
Entrez_Gene (NCBI)MTRNR2L7    MT-RNR2 like 7
AliasesHN7
GeneCards (Weizmann)MTRNR2L7
Ensembl hg19 (Hinxton)ENSG00000256892 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000256892 [Gene_View]  ENSG00000256892 [Sequence]  chr10:37601438-37602931 [Contig_View]  MTRNR2L7 [Vega]
ICGC DataPortalENSG00000256892
TCGA cBioPortalMTRNR2L7
AceView (NCBI)MTRNR2L7
Genatlas (Paris)MTRNR2L7
SOURCE (Princeton)MTRNR2L7
Genetics Home Reference (NIH)MTRNR2L7
Genomic and cartography
GoldenPath hg38 (UCSC)MTRNR2L7  -     chr10:37601438-37602931 -  10p11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MTRNR2L7  -     10p11.21   [Description]    (hg19-Feb_2009)
GoldenPathMTRNR2L7 - 10p11.21 [CytoView hg19]  MTRNR2L7 - 10p11.21 [CytoView hg38]
ImmunoBaseENSG00000256892
Genome Data Viewer NCBIMTRNR2L7 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001190489
Consensus coding sequences : CCDS (NCBI)MTRNR2L7
Gene ExpressionMTRNR2L7 [ NCBI-GEO ]   MTRNR2L7 [ EBI - ARRAY_EXPRESS ]   MTRNR2L7 [ SEEK ]   MTRNR2L7 [ MEM ]
Gene Expression Viewer (FireBrowse)MTRNR2L7 [ Firebrowse - Broad ]
GenevisibleExpression of MTRNR2L7 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100288485
GTEX Portal (Tissue expression)MTRNR2L7
Human Protein AtlasENSG00000256892-MTRNR2L7 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0CJ74   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0CJ74  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0CJ74
PhosPhoSitePlusP0CJ74
Domains : Interpro (EBI)Humanin   
Domain families : Pfam (Sanger)Humanin (PF15040)   
Domain families : Pfam (NCBI)pfam15040   
Conserved Domain (NCBI)MTRNR2L7
SuperfamilyP0CJ74
AlphaFold pdb e-kbP0CJ74   
Human Protein Atlas [tissue]ENSG00000256892-MTRNR2L7 [tissue]
Protein Interaction databases
DIP (DOE-UCLA)P0CJ74
IntAct (EBI)P0CJ74
BioGRIDMTRNR2L7
STRING (EMBL)MTRNR2L7
ZODIACMTRNR2L7
Ontologies - Pathways
QuickGOP0CJ74
Ontology : AmiGOextracellular region  cytoplasm  receptor antagonist activity  negative regulation of execution phase of apoptosis  negative regulation of signaling receptor activity  
Ontology : EGO-EBIextracellular region  cytoplasm  receptor antagonist activity  negative regulation of execution phase of apoptosis  negative regulation of signaling receptor activity  
NDEx NetworkMTRNR2L7
Atlas of Cancer Signalling NetworkMTRNR2L7
Wikipedia pathwaysMTRNR2L7
Orthology - Evolution
OrthoDB100288485
GeneTree (enSembl)ENSG00000256892
Phylogenetic Trees/Animal Genes : TreeFamMTRNR2L7
Homologs : HomoloGeneMTRNR2L7
Homology/Alignments : Family Browser (UCSC)MTRNR2L7
Gene fusions - Rearrangements
Fusion : QuiverMTRNR2L7
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMTRNR2L7 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MTRNR2L7
dbVarMTRNR2L7
ClinVarMTRNR2L7
MonarchMTRNR2L7
1000_GenomesMTRNR2L7 
Exome Variant ServerMTRNR2L7
GNOMAD BrowserENSG00000256892
Varsome BrowserMTRNR2L7
ACMGMTRNR2L7 variants
VarityP0CJ74
Genomic Variants (DGV)MTRNR2L7 [DGVbeta]
DECIPHERMTRNR2L7 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMTRNR2L7 
Mutations
ICGC Data PortalMTRNR2L7 
TCGA Data PortalMTRNR2L7 
Broad Tumor PortalMTRNR2L7
OASIS PortalMTRNR2L7 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMTRNR2L7  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DMTRNR2L7
Mutations and Diseases : HGMDMTRNR2L7
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaMTRNR2L7
DgiDB (Drug Gene Interaction Database)MTRNR2L7
DoCM (Curated mutations)MTRNR2L7
CIViC (Clinical Interpretations of Variants in Cancer)MTRNR2L7
Cancer3DMTRNR2L7
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETMTRNR2L7
MedgenMTRNR2L7
Genetic Testing Registry MTRNR2L7
NextProtP0CJ74 [Medical]
GENETestsMTRNR2L7
Target ValidationMTRNR2L7
Huge Navigator MTRNR2L7 [HugePedia]
ClinGenMTRNR2L7
Clinical trials, drugs, therapy
MyCancerGenomeMTRNR2L7
Protein Interactions : CTDMTRNR2L7
Pharm GKB GenePA165548890
PharosP0CJ74
Clinical trialMTRNR2L7
Miscellaneous
canSAR (ICR)MTRNR2L7
HarmonizomeMTRNR2L7
DataMed IndexMTRNR2L7
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXMTRNR2L7
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 16:12:03 CEST 2021

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