Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929441 (uncharacterized LOC101929441)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929441
Atlas_Id 67556
Location 1q32.1  [Link to chromosome band 1q32]
Location_base_pair Starts at 204141408 and ends at 204143009 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)LOC101929441  101929441  uncharacterized LOC101929441
Aliases
GeneCards (Weizmann)LOC101929441
Ensembl hg19 (Hinxton)ENSG00000230550 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000230550 [Gene_View]  chr1:204141408-204143009 [Contig_View]  LOC101929441 [Vega]
ICGC DataPortalENSG00000230550
TCGA cBioPortalLOC101929441
AceView (NCBI)LOC101929441
Genatlas (Paris)LOC101929441
WikiGenes101929441
SOURCE (Princeton)LOC101929441
Genetics Home Reference (NIH)LOC101929441
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929441  -     chr1:204141408-204143009 +  1q32.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929441  -     1q32.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929441 - 1q32.1 [CytoView hg19]  LOC101929441 - 1q32.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929441 [Mapview hg19]  LOC101929441 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC038769
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929441
Cluster EST : UnigeneHs.736889 [ NCBI ]
CGAP (NCI)Hs.736889
Alternative Splicing GalleryENSG00000230550
Gene ExpressionLOC101929441 [ NCBI-GEO ]   LOC101929441 [ EBI - ARRAY_EXPRESS ]   LOC101929441 [ SEEK ]   LOC101929441 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929441 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929441
GTEX Portal (Tissue expression)LOC101929441
Human Protein AtlasENSG00000230550-LOC101929441 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929441
DMDM Disease mutations101929441
Blocks (Seattle)LOC101929441
Human Protein Atlas [tissue]ENSG00000230550-LOC101929441 [tissue]
Protein Interaction databases
FunCoupENSG00000230550
BioGRIDLOC101929441
STRING (EMBL)LOC101929441
ZODIACLOC101929441
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929441
BioCentury BCIQLOC101929441
ClinGenLOC101929441
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929441
Clinical trialLOC101929441
Miscellaneous
canSAR (ICR)LOC101929441 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929441
EVEXLOC101929441
GoPubMedLOC101929441
iHOPLOC101929441
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 13:52:08 CET 2017

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