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LOC101928137 (uncharacterized LOC101928137)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928137
Atlas_Id 67289
Location 12q21.1  [Link to chromosome band 12q21]
Location_base_pair Starts at 73552970 and ends at 73602097 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)LOC101928137  101928137  uncharacterized LOC101928137
Aliases
GeneCards (Weizmann)LOC101928137
Ensembl hg19 (Hinxton)ENSG00000258123 [Gene_View]  chr12:73552970-73602097 [Contig_View]  LOC101928137 [Vega]
Ensembl hg38 (Hinxton)ENSG00000258123 [Gene_View]  chr12:73552970-73602097 [Contig_View]  LOC101928137 [Vega]
ICGC DataPortalENSG00000258123
TCGA cBioPortalLOC101928137
AceView (NCBI)LOC101928137
Genatlas (Paris)LOC101928137
WikiGenes101928137
SOURCE (Princeton)LOC101928137
Genetics Home Reference (NIH)LOC101928137
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101928137  -     chr12:73552970-73602097 +  12q21.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101928137  -     12q21.1   [Description]    (hg38-Dec_2013)
EnsemblLOC101928137 - 12q21.1 [CytoView hg19]  LOC101928137 - 12q21.1 [CytoView hg38]
Mapping of homologs : NCBILOC101928137 [Mapview hg19]  LOC101928137 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK310448 HG504970
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000012 NC_018923 NT_029419 NW_004929384
Consensus coding sequences : CCDS (NCBI)LOC101928137
Cluster EST : UnigeneHs.694666 [ NCBI ]
CGAP (NCI)Hs.694666
Alternative Splicing GalleryENSG00000258123
Gene ExpressionLOC101928137 [ NCBI-GEO ]   LOC101928137 [ EBI - ARRAY_EXPRESS ]   LOC101928137 [ SEEK ]   LOC101928137 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928137 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928137
GTEX Portal (Tissue expression)LOC101928137
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928137
DMDM Disease mutations101928137
Blocks (Seattle)LOC101928137
Human Protein AtlasENSG00000258123
Protein Interaction databases
FunCoupENSG00000258123
BioGRIDLOC101928137
STRING (EMBL)LOC101928137
ZODIACLOC101928137
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928137
BioCentury BCIQLOC101928137
ClinGenLOC101928137
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928137
Clinical trialLOC101928137
Miscellaneous
canSAR (ICR)LOC101928137 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928137
EVEXLOC101928137
GoPubMedLOC101928137
iHOPLOC101928137
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 12:19:18 CET 2017

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