Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929592 (uncharacterized LOC101929592)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929592
Atlas_Id 67593
Location 1p34.1  [Link to chromosome band 1p34]
Location_base_pair Starts at 44175076 and ends at 44193014 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)-   -
Cards
Entrez_Gene (NCBI)LOC101929592  101929592  uncharacterized LOC101929592
Aliases
GeneCards (Weizmann)LOC101929592
Ensembl hg19 (Hinxton)ENSG00000229444 [Gene_View]  chr1:44175076-44193014 [Contig_View]  LOC101929592 [Vega]
Ensembl hg38 (Hinxton)ENSG00000229444 [Gene_View]  chr1:44175076-44193014 [Contig_View]  LOC101929592 [Vega]
ICGC DataPortalENSG00000229444
TCGA cBioPortalLOC101929592
AceView (NCBI)LOC101929592
Genatlas (Paris)LOC101929592
WikiGenes101929592
SOURCE (Princeton)LOC101929592
Genetics Home Reference (NIH)LOC101929592
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101929592  -     chr1:44175076-44193014 -  1p34.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101929592  -     1p34.1   [Description]    (hg38-Dec_2013)
EnsemblLOC101929592 - 1p34.1 [CytoView hg19]  LOC101929592 - 1p34.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929592 [Mapview hg19]  LOC101929592 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX280555 HG491967
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000001 NC_018912 NG_028196 NT_032977 NW_004929290
Consensus coding sequences : CCDS (NCBI)LOC101929592
Alternative Splicing GalleryENSG00000229444
Gene ExpressionLOC101929592 [ NCBI-GEO ]   LOC101929592 [ EBI - ARRAY_EXPRESS ]   LOC101929592 [ SEEK ]   LOC101929592 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929592 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929592
GTEX Portal (Tissue expression)LOC101929592
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929592
DMDM Disease mutations101929592
Blocks (Seattle)LOC101929592
Human Protein AtlasENSG00000229444
Protein Interaction databases
FunCoupENSG00000229444
BioGRIDLOC101929592
STRING (EMBL)LOC101929592
ZODIACLOC101929592
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929592
BioCentury BCIQLOC101929592
ClinGenLOC101929592
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929592
Clinical trialLOC101929592
Miscellaneous
canSAR (ICR)LOC101929592 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929592
EVEXLOC101929592
GoPubMedLOC101929592
iHOPLOC101929592
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 Mar 14 12:20:49 CET 2017

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