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LOC105374729 (uncharacterized LOC105374729)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105374729
Atlas_Id 77884
Location 5p13.2  [Link to chromosome band 5p13]
Location_base_pair Starts at 37948593 and ends at 37951156 bp from pter ( according to hg19-Feb_2009)
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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC105374729  105374729  uncharacterized LOC105374729
Aliases
GeneCards (Weizmann)LOC105374729
Ensembl hg19 (Hinxton)ENSG00000251518 [Gene_View]  chr5:37948593-37951156 [Contig_View]  LOC105374729 [Vega]
Ensembl hg38 (Hinxton)ENSG00000251518 [Gene_View]  chr5:37948593-37951156 [Contig_View]  LOC105374729 [Vega]
ICGC DataPortalENSG00000251518
TCGA cBioPortalLOC105374729
AceView (NCBI)LOC105374729
Genatlas (Paris)LOC105374729
WikiGenes105374729
SOURCE (Princeton)LOC105374729
Genetics Home Reference (NIH)LOC105374729
Genomic and cartography
GoldenPath hg19 (UCSC)LOC105374729  -     chr5:37948593-37951156 +  5p13.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC105374729  -     5p13.2   [Description]    (hg38-Dec_2013)
EnsemblLOC105374729 - 5p13.2 [CytoView hg19]  LOC105374729 - 5p13.2 [CytoView hg38]
Mapping of homologs : NCBILOC105374729 [Mapview hg19]  LOC105374729 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000005 NC_018916 NT_006576 NW_004929321
Consensus coding sequences : CCDS (NCBI)LOC105374729
Cluster EST : UnigeneHs.738100 [ NCBI ]
CGAP (NCI)Hs.738100
Alternative Splicing GalleryENSG00000251518
Gene ExpressionLOC105374729 [ NCBI-GEO ]   LOC105374729 [ EBI - ARRAY_EXPRESS ]   LOC105374729 [ SEEK ]   LOC105374729 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105374729 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105374729
GTEX Portal (Tissue expression)LOC105374729
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105374729
DMDM Disease mutations105374729
Blocks (Seattle)LOC105374729
Human Protein AtlasENSG00000251518
Protein Interaction databases
FunCoupENSG00000251518
BioGRIDLOC105374729
STRING (EMBL)LOC105374729
ZODIACLOC105374729
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105374729
BioCentury BCIQLOC105374729
ClinGenLOC105374729
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105374729
Clinical trialLOC105374729
Miscellaneous
canSAR (ICR)LOC105374729 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105374729
EVEXLOC105374729
GoPubMedLOC105374729
iHOPLOC105374729
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 Mar 14 12:23:04 CET 2017

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