Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929099 (uncharacterized LOC101929099)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929099
Atlas_Id 67490
Location 1p13.1  [Link to chromosome band 1p13]
Location_base_pair Starts at 117025482 and ends at 117059490 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)LOC101929099  101929099  uncharacterized LOC101929099
Aliases
GeneCards (Weizmann)LOC101929099
Ensembl hg19 (Hinxton)ENSG00000236137 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000236137 [Gene_View]  chr1:117025482-117059490 [Contig_View]  LOC101929099 [Vega]
ICGC DataPortalENSG00000236137
TCGA cBioPortalLOC101929099
AceView (NCBI)LOC101929099
Genatlas (Paris)LOC101929099
WikiGenes101929099
SOURCE (Princeton)LOC101929099
Genetics Home Reference (NIH)LOC101929099
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929099  -     chr1:117025482-117059490 -  1p13.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929099  -     1p13.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929099 - 1p13.1 [CytoView hg19]  LOC101929099 - 1p13.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929099 [Mapview hg19]  LOC101929099 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK124329
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929099
Cluster EST : UnigeneHs.559118 [ NCBI ]
CGAP (NCI)Hs.559118
Alternative Splicing GalleryENSG00000236137
Gene ExpressionLOC101929099 [ NCBI-GEO ]   LOC101929099 [ EBI - ARRAY_EXPRESS ]   LOC101929099 [ SEEK ]   LOC101929099 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929099 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929099
GTEX Portal (Tissue expression)LOC101929099
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929099
DMDM Disease mutations101929099
Blocks (Seattle)LOC101929099
Human Protein AtlasENSG00000236137
Protein Interaction databases
FunCoupENSG00000236137
BioGRIDLOC101929099
STRING (EMBL)LOC101929099
ZODIACLOC101929099
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929099
BioCentury BCIQLOC101929099
ClinGenLOC101929099
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929099
Clinical trialLOC101929099
Miscellaneous
canSAR (ICR)LOC101929099 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929099
EVEXLOC101929099
GoPubMedLOC101929099
iHOPLOC101929099
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 : Wed Jun 7 16:06:01 CEST 2017

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