Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929162 (uncharacterized LOC101929162)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929162
Atlas_Id 67505
Location 12q23.3  [Link to chromosome band 12q23]
Location_base_pair Starts at 107736555 and ends at 107759968 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)LOC101929162  101929162  uncharacterized LOC101929162
Aliases
GeneCards (Weizmann)LOC101929162
Ensembl hg19 (Hinxton)ENSG00000258136 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258136 [Gene_View]  chr12:107736555-107759968 [Contig_View]  LOC101929162 [Vega]
ICGC DataPortalENSG00000258136
TCGA cBioPortalLOC101929162
AceView (NCBI)LOC101929162
Genatlas (Paris)LOC101929162
WikiGenes101929162
SOURCE (Princeton)LOC101929162
Genetics Home Reference (NIH)LOC101929162
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929162  -     chr12:107736555-107759968 +  12q23.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929162  -     12q23.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101929162 - 12q23.3 [CytoView hg19]  LOC101929162 - 12q23.3 [CytoView hg38]
Mapping of homologs : NCBILOC101929162 [Mapview hg19]  LOC101929162 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK093309 DB084413
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929162
Cluster EST : UnigeneHs.667028 [ NCBI ]
CGAP (NCI)Hs.667028
Alternative Splicing GalleryENSG00000258136
Gene ExpressionLOC101929162 [ NCBI-GEO ]   LOC101929162 [ EBI - ARRAY_EXPRESS ]   LOC101929162 [ SEEK ]   LOC101929162 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929162 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929162
GTEX Portal (Tissue expression)LOC101929162
Human Protein AtlasENSG00000258136-LOC101929162 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929162
DMDM Disease mutations101929162
Blocks (Seattle)LOC101929162
Human Protein Atlas [tissue]ENSG00000258136-LOC101929162 [tissue]
Protein Interaction databases
FunCoupENSG00000258136
BioGRIDLOC101929162
STRING (EMBL)LOC101929162
ZODIACLOC101929162
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929162
BioCentury BCIQLOC101929162
ClinGenLOC101929162
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929162
Clinical trialLOC101929162
Miscellaneous
canSAR (ICR)LOC101929162 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929162
EVEXLOC101929162
GoPubMedLOC101929162
iHOPLOC101929162
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:05:04 CET 2017

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