Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928441 (uncharacterized LOC101928441)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928441
Atlas_Id 67355
Location 12p12.1  [Link to chromosome band 12p12]
Location_base_pair Starts at 23175636 and ends at 23191587 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)LOC101928441  101928441  uncharacterized LOC101928441
Aliases
GeneCards (Weizmann)LOC101928441
Ensembl hg19 (Hinxton)ENSG00000256321 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000256321 [Gene_View]  chr12:23175636-23191587 [Contig_View]  LOC101928441 [Vega]
ICGC DataPortalENSG00000256321
TCGA cBioPortalLOC101928441
AceView (NCBI)LOC101928441
Genatlas (Paris)LOC101928441
WikiGenes101928441
SOURCE (Princeton)LOC101928441
Genetics Home Reference (NIH)LOC101928441
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928441  -     chr12:23175636-23191587 +  12p12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928441  -     12p12.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101928441 - 12p12.1 [CytoView hg19]  LOC101928441 - 12p12.1 [CytoView hg38]
Mapping of homologs : NCBILOC101928441 [Mapview hg19]  LOC101928441 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK058180 AL517295
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928441
Cluster EST : UnigeneHs.129111 [ NCBI ]
CGAP (NCI)Hs.129111
Alternative Splicing GalleryENSG00000256321
Gene ExpressionLOC101928441 [ NCBI-GEO ]   LOC101928441 [ EBI - ARRAY_EXPRESS ]   LOC101928441 [ SEEK ]   LOC101928441 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928441 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928441
GTEX Portal (Tissue expression)LOC101928441
Human Protein AtlasENSG00000256321-LOC101928441 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928441
DMDM Disease mutations101928441
Blocks (Seattle)LOC101928441
Human Protein Atlas [tissue]ENSG00000256321-LOC101928441 [tissue]
Protein Interaction databases
FunCoupENSG00000256321
BioGRIDLOC101928441
STRING (EMBL)LOC101928441
ZODIACLOC101928441
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928441
BioCentury BCIQLOC101928441
ClinGenLOC101928441
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928441
Clinical trialLOC101928441
Miscellaneous
canSAR (ICR)LOC101928441 (select the gene name)
Probes
Litterature
GeneRIFs
CoreMineLOC101928441
EVEXLOC101928441
GoPubMedLOC101928441
iHOPLOC101928441
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 : Thu Nov 9 12:04:21 CET 2017

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