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METTL26 (methyltransferase like 26)

Identity

Alias_namesC16orf13
chromosome 16 open reading frame 13
Alias_symbol (synonym)MGC13114
Other aliasJFP2
HGNC (Hugo) METTL26
LocusID (NCBI) 84326
Atlas_Id 78506
Location 16p13.3  [Link to chromosome band 16p13]
Location_base_pair Starts at 634427 and ends at 636366 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)METTL26   14141
Cards
Entrez_Gene (NCBI)METTL26  84326  methyltransferase like 26
AliasesC16orf13; JFP2
GeneCards (Weizmann)METTL26
Ensembl hg19 (Hinxton)ENSG00000130731 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000130731 [Gene_View]  chr16:634427-636366 [Contig_View]  METTL26 [Vega]
ICGC DataPortalENSG00000130731
TCGA cBioPortalMETTL26
AceView (NCBI)METTL26
Genatlas (Paris)METTL26
WikiGenes84326
SOURCE (Princeton)METTL26
Genetics Home Reference (NIH)METTL26
Genomic and cartography
GoldenPath hg38 (UCSC)METTL26  -     chr16:634427-636366 -  16p13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)METTL26  -     16p13.3   [Description]    (hg19-Feb_2009)
EnsemblMETTL26 - 16p13.3 [CytoView hg19]  METTL26 - 16p13.3 [CytoView hg38]
Mapping of homologs : NCBIMETTL26 [Mapview hg19]  METTL26 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI146806 AK057077 AK293046 AK294482 AK295628
RefSeq transcript (Entrez)NM_001040160 NM_001040161 NM_001040162 NM_001040163 NM_001040164 NM_001040165 NM_001040166 NM_001288710 NM_032366
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)METTL26
Cluster EST : UnigeneHs.239500 [ NCBI ]
CGAP (NCI)Hs.239500
Alternative Splicing GalleryENSG00000130731
Gene ExpressionMETTL26 [ NCBI-GEO ]   METTL26 [ EBI - ARRAY_EXPRESS ]   METTL26 [ SEEK ]   METTL26 [ MEM ]
Gene Expression Viewer (FireBrowse)METTL26 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)84326
GTEX Portal (Tissue expression)METTL26
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96S19   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96S19  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96S19
Splice isoforms : SwissVarQ96S19
PhosPhoSitePlusQ96S19
Domains : Interpro (EBI)DUF938    SAM-dependent_MTases   
Domain families : Pfam (Sanger)DUF938 (PF06080)   
Domain families : Pfam (NCBI)pfam06080   
Conserved Domain (NCBI)METTL26
DMDM Disease mutations84326
Blocks (Seattle)METTL26
SuperfamilyQ96S19
Human Protein AtlasENSG00000130731
Peptide AtlasQ96S19
HPRD17482
IPIIPI00745105   IPI00065475   IPI00893549   IPI00746178   IPI00747270   IPI00749346   
Protein Interaction databases
DIP (DOE-UCLA)Q96S19
IntAct (EBI)Q96S19
FunCoupENSG00000130731
BioGRIDMETTL26
STRING (EMBL)METTL26
ZODIACMETTL26
Ontologies - Pathways
QuickGOQ96S19
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkMETTL26
Atlas of Cancer Signalling NetworkMETTL26
Wikipedia pathwaysMETTL26
Orthology - Evolution
OrthoDB84326
GeneTree (enSembl)ENSG00000130731
Phylogenetic Trees/Animal Genes : TreeFamMETTL26
HOVERGENQ96S19
HOGENOMQ96S19
Homologs : HomoloGeneMETTL26
Homology/Alignments : Family Browser (UCSC)METTL26
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMETTL26 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)METTL26
dbVarMETTL26
ClinVarMETTL26
1000_GenomesMETTL26 
Exome Variant ServerMETTL26
ExAC (Exome Aggregation Consortium)METTL26 (select the gene name)
Genetic variants : HAPMAP84326
Genomic Variants (DGV)METTL26 [DGVbeta]
DECIPHERMETTL26 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMETTL26 
Mutations
ICGC Data PortalMETTL26 
TCGA Data PortalMETTL26 
Broad Tumor PortalMETTL26
OASIS PortalMETTL26 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDMETTL26
BioMutasearch METTL26
DgiDB (Drug Gene Interaction Database)METTL26
DoCM (Curated mutations)METTL26 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)METTL26 (select a term)
intoGenMETTL26
Cancer3DMETTL26(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMETTL26
Genetic Testing Registry METTL26
NextProtQ96S19 [Medical]
TSGene84326
GENETestsMETTL26
Target ValidationMETTL26
Huge Navigator METTL26 [HugePedia]
snp3D : Map Gene to Disease84326
BioCentury BCIQMETTL26
ClinGenMETTL26
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD84326
Chemical/Pharm GKB GenePA25526
Clinical trialMETTL26
Miscellaneous
canSAR (ICR)METTL26 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMETTL26
EVEXMETTL26
GoPubMedMETTL26
iHOPMETTL26
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 13:27:13 CEST 2017

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