Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929901 (uncharacterized LOC101929901)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929901
Atlas_Id 78570
Location 1p34.2  [Link to chromosome band 1p34]
Location_base_pair Starts at 41375004 and ends at 41375669 bp from pter ( according to hg38-Dec_2013)

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)LOC101929901  101929901  uncharacterized LOC101929901
Aliases
GeneCards (Weizmann)LOC101929901
Ensembl hg19 (Hinxton)ENSG00000229901 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000229901 [Gene_View]  chr1:41375004-41375669 [Contig_View]  LOC101929901 [Vega]
ICGC DataPortalENSG00000229901
TCGA cBioPortalLOC101929901
AceView (NCBI)LOC101929901
Genatlas (Paris)LOC101929901
WikiGenes101929901
SOURCE (Princeton)LOC101929901
Genetics Home Reference (NIH)LOC101929901
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929901  -     chr1:41375004-41375669 -  1p34.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929901  -     1p34.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101929901 - 1p34.2 [CytoView hg19]  LOC101929901 - 1p34.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929901 [Mapview hg19]  LOC101929901 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA574139
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929901
Alternative Splicing GalleryENSG00000229901
Gene ExpressionLOC101929901 [ NCBI-GEO ]   LOC101929901 [ EBI - ARRAY_EXPRESS ]   LOC101929901 [ SEEK ]   LOC101929901 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929901 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929901
GTEX Portal (Tissue expression)LOC101929901
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929901
DMDM Disease mutations101929901
Blocks (Seattle)LOC101929901
Human Protein AtlasENSG00000229901
Protein Interaction databases
FunCoupENSG00000229901
BioGRIDLOC101929901
STRING (EMBL)LOC101929901
ZODIACLOC101929901
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929901
BioCentury BCIQLOC101929901
ClinGenLOC101929901
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929901
Clinical trialLOC101929901
Miscellaneous
canSAR (ICR)LOC101929901 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929901
EVEXLOC101929901
GoPubMedLOC101929901
iHOPLOC101929901
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 : Mon Sep 18 13:21:59 CEST 2017

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