Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

LOC105377967 (uncharacterized LOC105377967)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105377967
Atlas_Id 78206
Location 6q22.2  [Link to chromosome band 6q22]
Location_base_pair Starts at 118085903 and ends at 118095472 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)LOC105377967  105377967  uncharacterized LOC105377967
Aliases
GeneCards (Weizmann)LOC105377967
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr6:118085903-118095472 [Contig_View]  LOC105377967 [Vega]
TCGA cBioPortalLOC105377967
AceView (NCBI)LOC105377967
Genatlas (Paris)LOC105377967
WikiGenes105377967
SOURCE (Princeton)LOC105377967
Genetics Home Reference (NIH)LOC105377967
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105377967  -     chr6:118085903-118095472 +  6q22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105377967  -     6q22.2   [Description]    (hg19-Feb_2009)
EnsemblLOC105377967 - 6q22.2 [CytoView hg19]  LOC105377967 - 6q22.2 [CytoView hg38]
Mapping of homologs : NCBILOC105377967 [Mapview hg19]  LOC105377967 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DB526410
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105377967
Cluster EST : UnigeneHs.692865 [ NCBI ]
CGAP (NCI)Hs.692865
Gene ExpressionLOC105377967 [ NCBI-GEO ]   LOC105377967 [ EBI - ARRAY_EXPRESS ]   LOC105377967 [ SEEK ]   LOC105377967 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105377967 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105377967
GTEX Portal (Tissue expression)LOC105377967
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105377967
DMDM Disease mutations105377967
Blocks (Seattle)LOC105377967
Protein Interaction databases
BioGRIDLOC105377967
STRING (EMBL)LOC105377967
ZODIACLOC105377967
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105377967
BioCentury BCIQLOC105377967
ClinGenLOC105377967
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105377967
Clinical trialLOC105377967
Miscellaneous
canSAR (ICR)LOC105377967 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105377967
EVEXLOC105377967
GoPubMedLOC105377967
iHOPLOC105377967
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 : Mon Jul 30 14:07:49 CEST 2018

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.