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

LOC100506178 (uncharacterized LOC100506178)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506178
Atlas_Id 66790
Location 7p15.3  [Link to chromosome band 7p15]
Location_base_pair Starts at 22563337 and ends at 22573998 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)LOC100506178  100506178  uncharacterized LOC100506178
Aliases
GeneCards (Weizmann)LOC100506178
Ensembl hg19 (Hinxton)ENSG00000232759 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000232759 [Gene_View]  chr7:22563337-22573998 [Contig_View]  LOC100506178 [Vega]
ICGC DataPortalENSG00000232759
TCGA cBioPortalLOC100506178
AceView (NCBI)LOC100506178
Genatlas (Paris)LOC100506178
WikiGenes100506178
SOURCE (Princeton)LOC100506178
Genetics Home Reference (NIH)LOC100506178
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506178  -     chr7:22563337-22573998 +  7p15.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506178  -     7p15.3   [Description]    (hg19-Feb_2009)
EnsemblLOC100506178 - 7p15.3 [CytoView hg19]  LOC100506178 - 7p15.3 [CytoView hg38]
Mapping of homologs : NCBILOC100506178 [Mapview hg19]  LOC100506178 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK123961 DA428433
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506178
Cluster EST : UnigeneHs.668122 [ NCBI ]
CGAP (NCI)Hs.668122
Alternative Splicing GalleryENSG00000232759
Gene ExpressionLOC100506178 [ NCBI-GEO ]   LOC100506178 [ EBI - ARRAY_EXPRESS ]   LOC100506178 [ SEEK ]   LOC100506178 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506178 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506178
GTEX Portal (Tissue expression)LOC100506178
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506178
DMDM Disease mutations100506178
Blocks (Seattle)LOC100506178
Human Protein AtlasENSG00000232759
Protein Interaction databases
FunCoupENSG00000232759
BioGRIDLOC100506178
STRING (EMBL)LOC100506178
ZODIACLOC100506178
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506178
BioCentury BCIQLOC100506178
ClinGenLOC100506178
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506178
Clinical trialLOC100506178
Miscellaneous
canSAR (ICR)LOC100506178 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506178
EVEXLOC100506178
GoPubMedLOC100506178
iHOPLOC100506178
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 : Wed Jun 7 16:02:33 CEST 2017

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.