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MAP3K7CL (MAP3K7 C-terminal like)

Identity

Alias (NCBI)C21orf7
HC21ORF7
TAK1L
TAKL
TAKL-1
TAKL-2
TAKL-4
HGNC (Hugo) MAP3K7CL
HGNC Alias symbTAKL
TAK1L
TAKL-1
TAKL-2
TAKL-4
HGNC Previous nameC21orf7
HGNC Previous namechromosome 21 open reading frame 7
LocusID (NCBI) 56911
Atlas_Id 68795
Location 21q21.3  [Link to chromosome band 21q21]
Location_base_pair Starts at 29077114 and ends at 29175887 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)
BACH1 (21q21.3) / MAP3K7CL (21q21.3)SNAPC3 (9p22.3) / MAP3K7CL (21q21.3)

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)MAP3K7CL   16457
Cards
Entrez_Gene (NCBI)MAP3K7CL    MAP3K7 C-terminal like
AliasesC21orf7; HC21ORF7; TAK1L; TAKL; 
TAKL-1; TAKL-2; TAKL-4
GeneCards (Weizmann)MAP3K7CL
Ensembl hg19 (Hinxton)ENSG00000156265 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000156265 [Gene_View]  ENSG00000156265 [Sequence]  chr21:29077114-29175887 [Contig_View]  MAP3K7CL [Vega]
ICGC DataPortalENSG00000156265
TCGA cBioPortalMAP3K7CL
AceView (NCBI)MAP3K7CL
Genatlas (Paris)MAP3K7CL
SOURCE (Princeton)MAP3K7CL
Genetics Home Reference (NIH)MAP3K7CL
Genomic and cartography
GoldenPath hg38 (UCSC)MAP3K7CL  -     chr21:29077114-29175887 +  21q21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MAP3K7CL  -     21q21.3   [Description]    (hg19-Feb_2009)
GoldenPathMAP3K7CL - 21q21.3 [CytoView hg19]  MAP3K7CL - 21q21.3 [CytoView hg38]
ImmunoBaseENSG00000156265
Genome Data Viewer NCBIMAP3K7CL [Mapview hg19]  
OMIM611110   
Gene and transcription
Genbank (Entrez)AF269161 AF269162 AF269163 AF269164 AK056341
RefSeq transcript (Entrez)NM_001286617 NM_001286618 NM_001286619 NM_001286620 NM_001286622 NM_001286623 NM_001286624 NM_001286634 NM_001371369 NM_001371370 NM_001371371 NM_001371372 NM_001371373 NM_001371374 NM_001371376 NM_020152
Consensus coding sequences : CCDS (NCBI)MAP3K7CL
Gene ExpressionMAP3K7CL [ NCBI-GEO ]   MAP3K7CL [ EBI - ARRAY_EXPRESS ]   MAP3K7CL [ SEEK ]   MAP3K7CL [ MEM ]
Gene Expression Viewer (FireBrowse)MAP3K7CL [ Firebrowse - Broad ]
GenevisibleExpression of MAP3K7CL in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)56911
GTEX Portal (Tissue expression)MAP3K7CL
Human Protein AtlasENSG00000156265-MAP3K7CL [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP57077   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP57077  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP57077
PhosPhoSitePlusP57077
Domains : Interpro (EBI)Map3k7cl   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MAP3K7CL
SuperfamilyP57077
AlphaFold pdb e-kbP57077   
Human Protein Atlas [tissue]ENSG00000156265-MAP3K7CL [tissue]
HPRD10764
Protein Interaction databases
DIP (DOE-UCLA)P57077
IntAct (EBI)P57077
BioGRIDMAP3K7CL
STRING (EMBL)MAP3K7CL
ZODIACMAP3K7CL
Ontologies - Pathways
QuickGOP57077
Ontology : AmiGOprotein binding  nucleus  cytosol  
Ontology : EGO-EBIprotein binding  nucleus  cytosol  
NDEx NetworkMAP3K7CL
Atlas of Cancer Signalling NetworkMAP3K7CL
Wikipedia pathwaysMAP3K7CL
Orthology - Evolution
OrthoDB56911
GeneTree (enSembl)ENSG00000156265
Phylogenetic Trees/Animal Genes : TreeFamMAP3K7CL
Homologs : HomoloGeneMAP3K7CL
Homology/Alignments : Family Browser (UCSC)MAP3K7CL
Gene fusions - Rearrangements
Fusion : QuiverMAP3K7CL
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMAP3K7CL [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MAP3K7CL
dbVarMAP3K7CL
ClinVarMAP3K7CL
MonarchMAP3K7CL
1000_GenomesMAP3K7CL 
Exome Variant ServerMAP3K7CL
GNOMAD BrowserENSG00000156265
Varsome BrowserMAP3K7CL
ACMGMAP3K7CL variants
VarityP57077
Genomic Variants (DGV)MAP3K7CL [DGVbeta]
DECIPHERMAP3K7CL [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMAP3K7CL 
Mutations
ICGC Data PortalMAP3K7CL 
TCGA Data PortalMAP3K7CL 
Broad Tumor PortalMAP3K7CL
OASIS PortalMAP3K7CL [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMAP3K7CL  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DMAP3K7CL
Mutations and Diseases : HGMDMAP3K7CL
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaMAP3K7CL
DgiDB (Drug Gene Interaction Database)MAP3K7CL
DoCM (Curated mutations)MAP3K7CL
CIViC (Clinical Interpretations of Variants in Cancer)MAP3K7CL
Cancer3DMAP3K7CL
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM611110   
Orphanet
DisGeNETMAP3K7CL
MedgenMAP3K7CL
Genetic Testing Registry MAP3K7CL
NextProtP57077 [Medical]
GENETestsMAP3K7CL
Target ValidationMAP3K7CL
Huge Navigator MAP3K7CL [HugePedia]
ClinGenMAP3K7CL
Clinical trials, drugs, therapy
MyCancerGenomeMAP3K7CL
Protein Interactions : CTDMAP3K7CL
Pharm GKB GenePA25864
PharosP57077
Clinical trialMAP3K7CL
Miscellaneous
canSAR (ICR)MAP3K7CL
HarmonizomeMAP3K7CL
DataMed IndexMAP3K7CL
Probes
Litterature
PubMed21 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXMAP3K7CL
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 16:06:51 CEST 2021

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