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METTL14 (methyltransferase like 14)

Identity

Alias_symbol (synonym)KIAA1627
Other alias-
HGNC (Hugo) METTL14
LocusID (NCBI) 57721
Atlas_Id 68912
Location 4q26  [Link to chromosome band 4q26]
Location_base_pair Starts at 119606525 and ends at 119633425 bp from pter ( according to hg19-Feb_2009)

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)METTL14   29330
Cards
Entrez_Gene (NCBI)METTL14  57721  methyltransferase like 14
Aliases
GeneCards (Weizmann)METTL14
Ensembl hg19 (Hinxton) [Gene_View]  chr4:119606525-119633425 [Contig_View]  METTL14 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr4:119606525-119633425 [Contig_View]  METTL14 [Vega]
TCGA cBioPortalMETTL14
AceView (NCBI)METTL14
Genatlas (Paris)METTL14
WikiGenes57721
SOURCE (Princeton)METTL14
Genetics Home Reference (NIH)METTL14
Genomic and cartography
GoldenPath hg19 (UCSC)METTL14  -     chr4:119606525-119633425 +  4q26   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)METTL14  -     4q26   [Description]    (hg38-Dec_2013)
EnsemblMETTL14 - 4q26 [CytoView hg19]  METTL14 - 4q26 [CytoView hg38]
Mapping of homologs : NCBIMETTL14 [Mapview hg19]  METTL14 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB046847 AK055555 AK296056 AW206149 BC006565
RefSeq transcript (Entrez)NM_020961
RefSeq genomic (Entrez)NC_000004 NC_018915 NT_016354 NW_004929320
Consensus coding sequences : CCDS (NCBI)METTL14
Cluster EST : UnigeneHs.657806 [ NCBI ]
CGAP (NCI)Hs.657806
Gene ExpressionMETTL14 [ NCBI-GEO ]   METTL14 [ EBI - ARRAY_EXPRESS ]   METTL14 [ SEEK ]   METTL14 [ MEM ]
Gene Expression Viewer (FireBrowse)METTL14 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57721
GTEX Portal (Tissue expression)METTL14
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9HCE5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9HCE5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9HCE5
Splice isoforms : SwissVarQ9HCE5
PhosPhoSitePlusQ9HCE5
Domaine pattern : Prosite (Expaxy)MT_A70 (PS51143)   
Domains : Interpro (EBI)MT-A70-like    SAM-dependent_MTases   
Domain families : Pfam (Sanger)MT-A70 (PF05063)   
Domain families : Pfam (NCBI)pfam05063   
Conserved Domain (NCBI)METTL14
DMDM Disease mutations57721
Blocks (Seattle)METTL14
SuperfamilyQ9HCE5
Peptide AtlasQ9HCE5
HPRD13879
IPIIPI00783133   IPI00965354   IPI00965557   
Protein Interaction databases
DIP (DOE-UCLA)Q9HCE5
IntAct (EBI)Q9HCE5
BioGRIDMETTL14
STRING (EMBL)METTL14
ZODIACMETTL14
Ontologies - Pathways
QuickGOQ9HCE5
Ontology : AmiGOmRNA splicing, via spliceosome  RNA binding  nucleus  nucleoplasm  mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity  stem cell maintenance  MIS complex  mRNA destabilization  mRNA methylation  
Ontology : EGO-EBImRNA splicing, via spliceosome  RNA binding  nucleus  nucleoplasm  mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity  stem cell maintenance  MIS complex  mRNA destabilization  mRNA methylation  
NDEx NetworkMETTL14
Atlas of Cancer Signalling NetworkMETTL14
Wikipedia pathwaysMETTL14
Orthology - Evolution
OrthoDB57721
Phylogenetic Trees/Animal Genes : TreeFamMETTL14
HOVERGENQ9HCE5
HOGENOMQ9HCE5
Homologs : HomoloGeneMETTL14
Homology/Alignments : Family Browser (UCSC)METTL14
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMETTL14 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)METTL14
dbVarMETTL14
ClinVarMETTL14
1000_GenomesMETTL14 
Exome Variant ServerMETTL14
ExAC (Exome Aggregation Consortium)METTL14 (select the gene name)
Genetic variants : HAPMAP57721
Genomic Variants (DGV)METTL14 [DGVbeta]
DECIPHER (Syndromes)4:119606525-119633425  
CONAN: Copy Number AnalysisMETTL14 
Mutations
ICGC Data PortalMETTL14 
TCGA Data PortalMETTL14 
Broad Tumor PortalMETTL14
OASIS PortalMETTL14 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMETTL14  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMETTL14
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch METTL14
DgiDB (Drug Gene Interaction Database)METTL14
DoCM (Curated mutations)METTL14 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)METTL14 (select a term)
intoGenMETTL14
Cancer3DMETTL14(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMETTL14
Genetic Testing Registry METTL14
NextProtQ9HCE5 [Medical]
TSGene57721
GENETestsMETTL14
Huge Navigator METTL14 [HugePedia]
snp3D : Map Gene to Disease57721
BioCentury BCIQMETTL14
ClinGenMETTL14
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD57721
Chemical/Pharm GKB GenePA164722277
Clinical trialMETTL14
Miscellaneous
canSAR (ICR)METTL14 (select the gene name)
Probes
Litterature
PubMed13 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMETTL14
EVEXMETTL14
GoPubMedMETTL14
iHOPMETTL14
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 12:28:04 CET 2017

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