Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929541 (uncharacterized LOC101929541)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929541
Atlas_Id 67579
Location 1q32.3  [Link to chromosome band 1q32]
Location_base_pair Starts at 212213002 and ends at 212234736 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)-   -
Cards
Entrez_Gene (NCBI)LOC101929541  101929541  uncharacterized LOC101929541
Aliases
GeneCards (Weizmann)LOC101929541
Ensembl hg19 (Hinxton)ENSG00000226251 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000226251 [Gene_View]  chr1:212213002-212234736 [Contig_View]  LOC101929541 [Vega]
ICGC DataPortalENSG00000226251
TCGA cBioPortalLOC101929541
AceView (NCBI)LOC101929541
Genatlas (Paris)LOC101929541
WikiGenes101929541
SOURCE (Princeton)LOC101929541
Genetics Home Reference (NIH)LOC101929541
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929541  -     chr1:212213002-212234736 -  1q32.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929541  -     1q32.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101929541 - 1q32.3 [CytoView hg19]  LOC101929541 - 1q32.3 [CytoView hg38]
Mapping of homologs : NCBILOC101929541 [Mapview hg19]  LOC101929541 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX099738 DA898365 F26527
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929541
Cluster EST : UnigeneHs.632493 [ NCBI ]
CGAP (NCI)Hs.632493
Alternative Splicing GalleryENSG00000226251
Gene ExpressionLOC101929541 [ NCBI-GEO ]   LOC101929541 [ EBI - ARRAY_EXPRESS ]   LOC101929541 [ SEEK ]   LOC101929541 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929541 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929541
GTEX Portal (Tissue expression)LOC101929541
Human Protein AtlasENSG00000226251-LOC101929541 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929541
DMDM Disease mutations101929541
Blocks (Seattle)LOC101929541
Human Protein Atlas [tissue]ENSG00000226251-LOC101929541 [tissue]
Protein Interaction databases
FunCoupENSG00000226251
BioGRIDLOC101929541
STRING (EMBL)LOC101929541
ZODIACLOC101929541
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929541
BioCentury BCIQLOC101929541
ClinGenLOC101929541
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929541
Clinical trialLOC101929541
Miscellaneous
canSAR (ICR)LOC101929541 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929541
EVEXLOC101929541
GoPubMedLOC101929541
iHOPLOC101929541
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Nov 20 19:48:39 CET 2017

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