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LOC105378614 (uncharacterized LOC105378614)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105378614
Atlas_Id 78408
Location 1p36.13  [Link to chromosome band 1p36]
Location_base_pair Starts at 19591802 and ends at 19596832 bp from pter ( according to hg38-Dec_2013)

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)LOC105378614  105378614  uncharacterized LOC105378614
Aliases
GeneCards (Weizmann)LOC105378614
Ensembl hg19 (Hinxton)ENSG00000235185 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000235185 [Gene_View]  chr1:19591802-19596832 [Contig_View]  LOC105378614 [Vega]
ICGC DataPortalENSG00000235185
TCGA cBioPortalLOC105378614
AceView (NCBI)LOC105378614
Genatlas (Paris)LOC105378614
WikiGenes105378614
SOURCE (Princeton)LOC105378614
Genetics Home Reference (NIH)LOC105378614
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105378614  -     chr1:19591802-19596832 -  1p36.13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105378614  -     1p36.13   [Description]    (hg19-Feb_2009)
EnsemblLOC105378614 - 1p36.13 [CytoView hg19]  LOC105378614 - 1p36.13 [CytoView hg38]
Mapping of homologs : NCBILOC105378614 [Mapview hg19]  LOC105378614 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI791463 BX106629
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105378614
Cluster EST : UnigeneHs.430098 [ NCBI ]
CGAP (NCI)Hs.430098
Alternative Splicing GalleryENSG00000235185
Gene ExpressionLOC105378614 [ NCBI-GEO ]   LOC105378614 [ EBI - ARRAY_EXPRESS ]   LOC105378614 [ SEEK ]   LOC105378614 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105378614 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105378614
GTEX Portal (Tissue expression)LOC105378614
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105378614
DMDM Disease mutations105378614
Blocks (Seattle)LOC105378614
Human Protein AtlasENSG00000235185
Protein Interaction databases
FunCoupENSG00000235185
BioGRIDLOC105378614
STRING (EMBL)LOC105378614
ZODIACLOC105378614
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105378614
BioCentury BCIQLOC105378614
ClinGenLOC105378614
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105378614
Clinical trialLOC105378614
Miscellaneous
canSAR (ICR)LOC105378614 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105378614
EVEXLOC105378614
GoPubMedLOC105378614
iHOPLOC105378614
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 Sep 18 13:24:06 CEST 2017

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