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WNT7B (Wnt family member 7B)

Identity

Alias_nameswingless-type MMTV integration site family, member 7B
Other alias-
HGNC (Hugo) WNT7B
LocusID (NCBI) 7477
Atlas_Id 42829
Location 22q13.31  [Link to chromosome band 22q13]
Location_base_pair Starts at 45920366 and ends at 45977128 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)
PSMC4 (19q13.2) / WNT7B (22q13.31)WNT7B (22q13.31) / DGCR8 (22q11.21)WNT7B 22q13.31 / DGCR8 22q11.21

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

 


Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 1 ]

Solid Tumors TT_t2222q11q13ID104859


External links

Nomenclature
HGNC (Hugo)WNT7B   12787
Cards
Entrez_Gene (NCBI)WNT7B  7477  Wnt family member 7B
Aliases
GeneCards (Weizmann)WNT7B
Ensembl hg19 (Hinxton)ENSG00000188064 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000188064 [Gene_View]  ENSG00000188064 [Sequence]  chr22:45920366-45977128 [Contig_View]  WNT7B [Vega]
ICGC DataPortalENSG00000188064
TCGA cBioPortalWNT7B
AceView (NCBI)WNT7B
Genatlas (Paris)WNT7B
WikiGenes7477
SOURCE (Princeton)WNT7B
Genetics Home Reference (NIH)WNT7B
Genomic and cartography
GoldenPath hg38 (UCSC)WNT7B  -     chr22:45920366-45977128 -  22q13.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)WNT7B  -     22q13.31   [Description]    (hg19-Feb_2009)
GoldenPathWNT7B - 22q13.31 [CytoView hg19]  WNT7B - 22q13.31 [CytoView hg38]
ImmunoBaseENSG00000188064
Mapping of homologs : NCBIWNT7B [Mapview hg19]  WNT7B [Mapview hg38]
OMIM601967   
Gene and transcription
Genbank (Entrez)AB062766 AF416743 AK123019 AK289526 BC034923
RefSeq transcript (Entrez)NM_058238
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)WNT7B
Alternative Splicing GalleryENSG00000188064
Gene ExpressionWNT7B [ NCBI-GEO ]   WNT7B [ EBI - ARRAY_EXPRESS ]   WNT7B [ SEEK ]   WNT7B [ MEM ]
Gene Expression Viewer (FireBrowse)WNT7B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)7477
GTEX Portal (Tissue expression)WNT7B
Human Protein AtlasENSG00000188064-WNT7B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)WNT7B
DMDM Disease mutations7477
Blocks (Seattle)WNT7B
Human Protein Atlas [tissue]ENSG00000188064-WNT7B [tissue]
HPRD03573
IPIIPI00011031   IPI00917719   IPI00876998   IPI00917468   IPI00917295   
Protein Interaction databases
FunCoupENSG00000188064
BioGRIDWNT7B
STRING (EMBL)WNT7B
ZODIACWNT7B
Ontologies - Pathways
Huge Navigator WNT7B [HugePedia]
snp3D : Map Gene to Disease7477
BioCentury BCIQWNT7B
ClinGenWNT7B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD7477
Chemical/Pharm GKB GenePA37388
Clinical trialWNT7B
Miscellaneous
canSAR (ICR)WNT7B (select the gene name)
DataMed IndexWNT7B
Probes
Litterature
PubMed39 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineWNT7B
EVEXWNT7B
GoPubMedWNT7B
iHOPWNT7B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Feb 19 17:16:42 CET 2020

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