Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC105369921 (uncharacterized LOC105369921)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105369921
Atlas_Id 78231
Location 12q22  [Link to chromosome band 12q22]
Location_base_pair Starts at 95795345 and ends at 95858839 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)LOC105369921  105369921  uncharacterized LOC105369921
Aliases
GeneCards (Weizmann)LOC105369921
Ensembl hg19 (Hinxton)ENSG00000258343 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258343 [Gene_View]  chr12:95795345-95858839 [Contig_View]  LOC105369921 [Vega]
ICGC DataPortalENSG00000258343
TCGA cBioPortalLOC105369921
AceView (NCBI)LOC105369921
Genatlas (Paris)LOC105369921
WikiGenes105369921
SOURCE (Princeton)LOC105369921
Genetics Home Reference (NIH)LOC105369921
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105369921  -     chr12:95795345-95858839 -  12q22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105369921  -     12q22   [Description]    (hg19-Feb_2009)
EnsemblLOC105369921 - 12q22 [CytoView hg19]  LOC105369921 - 12q22 [CytoView hg38]
Mapping of homologs : NCBILOC105369921 [Mapview hg19]  LOC105369921 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA884114 AI829734 BX107766 DB454575
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105369921
Cluster EST : UnigeneHs.739969 [ NCBI ]
CGAP (NCI)Hs.739969
Alternative Splicing GalleryENSG00000258343
Gene ExpressionLOC105369921 [ NCBI-GEO ]   LOC105369921 [ EBI - ARRAY_EXPRESS ]   LOC105369921 [ SEEK ]   LOC105369921 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105369921 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105369921
GTEX Portal (Tissue expression)LOC105369921
Human Protein AtlasENSG00000258343-LOC105369921 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105369921
DMDM Disease mutations105369921
Blocks (Seattle)LOC105369921
Human Protein Atlas [tissue]ENSG00000258343-LOC105369921 [tissue]
Protein Interaction databases
FunCoupENSG00000258343
BioGRIDLOC105369921
STRING (EMBL)LOC105369921
ZODIACLOC105369921
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105369921
BioCentury BCIQLOC105369921
ClinGenLOC105369921
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105369921
Clinical trialLOC105369921
Miscellaneous
canSAR (ICR)LOC105369921 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105369921
EVEXLOC105369921
GoPubMedLOC105369921
iHOPLOC105369921
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 Nov 21 13:53:36 CET 2017

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