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LOC101928449 (uncharacterized LOC101928449)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928449
Atlas_Id 67360
Location 12q21.31  [Link to chromosome band 12q21]
Location_base_pair Starts at 82347498 and ends at 82386912 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)LOC101928449  101928449  uncharacterized LOC101928449
Aliases
GeneCards (Weizmann)LOC101928449
Ensembl hg19 (Hinxton)ENSG00000257747 [Gene_View]  chr12:82347498-82386912 [Contig_View]  LOC101928449 [Vega]
Ensembl hg38 (Hinxton)ENSG00000257747 [Gene_View]  chr12:82347498-82386912 [Contig_View]  LOC101928449 [Vega]
ICGC DataPortalENSG00000257747
TCGA cBioPortalLOC101928449
AceView (NCBI)LOC101928449
Genatlas (Paris)LOC101928449
WikiGenes101928449
SOURCE (Princeton)LOC101928449
Genetics Home Reference (NIH)LOC101928449
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101928449  -     chr12:82347498-82386912 +  12q21.31   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101928449  -     12q21.31   [Description]    (hg38-Dec_2013)
EnsemblLOC101928449 - 12q21.31 [CytoView hg19]  LOC101928449 - 12q21.31 [CytoView hg38]
Mapping of homologs : NCBILOC101928449 [Mapview hg19]  LOC101928449 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC031963 HG505036
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000012 NC_018923 NT_029419 NW_004929384
Consensus coding sequences : CCDS (NCBI)LOC101928449
Cluster EST : UnigeneHs.737488 [ NCBI ]
CGAP (NCI)Hs.737488
Alternative Splicing GalleryENSG00000257747
Gene ExpressionLOC101928449 [ NCBI-GEO ]   LOC101928449 [ EBI - ARRAY_EXPRESS ]   LOC101928449 [ SEEK ]   LOC101928449 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928449 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928449
GTEX Portal (Tissue expression)LOC101928449
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928449
DMDM Disease mutations101928449
Blocks (Seattle)LOC101928449
Human Protein AtlasENSG00000257747
Protein Interaction databases
FunCoupENSG00000257747
BioGRIDLOC101928449
STRING (EMBL)LOC101928449
ZODIACLOC101928449
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928449
BioCentury BCIQLOC101928449
ClinGenLOC101928449
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928449
Clinical trialLOC101928449
Miscellaneous
canSAR (ICR)LOC101928449 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928449
EVEXLOC101928449
GoPubMedLOC101928449
iHOPLOC101928449
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 12:19:40 CET 2017

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