Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC105377448 (uncharacterized LOC105377448)

Identity

Alias (NCBI)-
HGNC (Hugo) -
LocusID (NCBI) 105377448
Atlas_Id 77898
Location 4q31.1  [Link to chromosome band 4q31]
Location_base_pair Starts at 138819957 and ends at 139012646 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)LOC105377448  105377448  uncharacterized LOC105377448
Aliases
GeneCards (Weizmann)LOC105377448
Ensembl hg19 (Hinxton)ENSG00000250195 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000250195 [Gene_View]  ENSG00000250195 [Sequence]  chr4:138819957-139012646 [Contig_View]  LOC105377448 [Vega]
ICGC DataPortalENSG00000250195
TCGA cBioPortalLOC105377448
AceView (NCBI)LOC105377448
Genatlas (Paris)LOC105377448
WikiGenes105377448
SOURCE (Princeton)LOC105377448
Genetics Home Reference (NIH)LOC105377448
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105377448  -     chr4:138819957-139012646 -  4q31.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105377448  -     4q31.1   [Description]    (hg19-Feb_2009)
GoldenPathLOC105377448 - 4q31.1 [CytoView hg19]  LOC105377448 - 4q31.1 [CytoView hg38]
ImmunoBaseENSG00000250195
genome Data Viewer NCBILOC105377448 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AI674379 BX115310
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105377448
Alternative Splicing GalleryENSG00000250195
Gene ExpressionLOC105377448 [ NCBI-GEO ]   LOC105377448 [ EBI - ARRAY_EXPRESS ]   LOC105377448 [ SEEK ]   LOC105377448 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105377448 [ Firebrowse - Broad ]
GenevisibleExpression of LOC105377448 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)105377448
GTEX Portal (Tissue expression)LOC105377448
Human Protein AtlasENSG00000250195-LOC105377448 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105377448
DMDM Disease mutations105377448
Blocks (Seattle)LOC105377448
Human Protein Atlas [tissue]ENSG00000250195-LOC105377448 [tissue]
Protein Interaction databases
FunCoupENSG00000250195
BioGRIDLOC105377448
STRING (EMBL)LOC105377448
ZODIACLOC105377448
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105377448
BioCentury BCIQLOC105377448
ClinGenLOC105377448
Clinical trials, drugs, therapy
Protein Interactions : CTD105377448
Clinical trialLOC105377448
Miscellaneous
canSAR (ICR)LOC105377448 (select the gene name)
HarmonizomeLOC105377448
DataMed IndexLOC105377448
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105377448
EVEXLOC105377448
GoPubMedLOC105377448
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 : Sat Aug 22 19:22:48 CEST 2020

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