Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929771 (uncharacterized LOC101929771)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929771
Atlas_Id 67635
Location 1q41  [Link to chromosome band 1q41]
Location_base_pair Starts at 222001008 and ends at 222014008 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)LOC101929771  101929771  uncharacterized LOC101929771
Aliases
GeneCards (Weizmann)LOC101929771
Ensembl hg19 (Hinxton)ENSG00000227925 [Gene_View]  chr1:222001008-222014008 [Contig_View]  LOC101929771 [Vega]
Ensembl hg38 (Hinxton)ENSG00000227925 [Gene_View]  chr1:222001008-222014008 [Contig_View]  LOC101929771 [Vega]
ICGC DataPortalENSG00000227925
TCGA cBioPortalLOC101929771
AceView (NCBI)LOC101929771
Genatlas (Paris)LOC101929771
WikiGenes101929771
SOURCE (Princeton)LOC101929771
Genetics Home Reference (NIH)LOC101929771
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101929771  -     chr1:222001008-222014008 -  1q41   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101929771  -     1q41   [Description]    (hg38-Dec_2013)
EnsemblLOC101929771 - 1q41 [CytoView hg19]  LOC101929771 - 1q41 [CytoView hg38]
Mapping of homologs : NCBILOC101929771 [Mapview hg19]  LOC101929771 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA782022 HG493235
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_004487 NW_004929294
Consensus coding sequences : CCDS (NCBI)LOC101929771
Cluster EST : UnigeneHs.557001 [ NCBI ]
CGAP (NCI)Hs.557001
Alternative Splicing GalleryENSG00000227925
Gene ExpressionLOC101929771 [ NCBI-GEO ]   LOC101929771 [ EBI - ARRAY_EXPRESS ]   LOC101929771 [ SEEK ]   LOC101929771 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929771 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929771
GTEX Portal (Tissue expression)LOC101929771
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929771
DMDM Disease mutations101929771
Blocks (Seattle)LOC101929771
Human Protein AtlasENSG00000227925
Protein Interaction databases
FunCoupENSG00000227925
BioGRIDLOC101929771
STRING (EMBL)LOC101929771
ZODIACLOC101929771
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929771
BioCentury BCIQLOC101929771
ClinGenLOC101929771
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929771
Clinical trialLOC101929771
Miscellaneous
canSAR (ICR)LOC101929771 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929771
EVEXLOC101929771
GoPubMedLOC101929771
iHOPLOC101929771
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 12:21:01 CET 2017

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