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

LOC100506098 (uncharacterized LOC100506098)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506098
Atlas_Id 78122
Location 7p21.1  [Link to chromosome band 7p21]
Location_base_pair Starts at 20217577 and ends at 20221699 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)LOC100506098  100506098  uncharacterized LOC100506098
Aliases
GeneCards (Weizmann)LOC100506098
Ensembl hg19 (Hinxton)ENSG00000233834 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000233834 [Gene_View]  chr7:20217577-20221699 [Contig_View]  LOC100506098 [Vega]
ICGC DataPortalENSG00000233834
TCGA cBioPortalLOC100506098
AceView (NCBI)LOC100506098
Genatlas (Paris)LOC100506098
WikiGenes100506098
SOURCE (Princeton)LOC100506098
Genetics Home Reference (NIH)LOC100506098
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506098  -     chr7:20217577-20221699 +  7p21.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506098  -     7p21.1   [Description]    (hg19-Feb_2009)
EnsemblLOC100506098 - 7p21.1 [CytoView hg19]  LOC100506098 - 7p21.1 [CytoView hg38]
Mapping of homologs : NCBILOC100506098 [Mapview hg19]  LOC100506098 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI928513 BG777800 BI759100 DR423379
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506098
Cluster EST : UnigeneHs.59203 [ NCBI ]
CGAP (NCI)Hs.59203
Alternative Splicing GalleryENSG00000233834
Gene ExpressionLOC100506098 [ NCBI-GEO ]   LOC100506098 [ EBI - ARRAY_EXPRESS ]   LOC100506098 [ SEEK ]   LOC100506098 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506098 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506098
GTEX Portal (Tissue expression)LOC100506098
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506098
DMDM Disease mutations100506098
Blocks (Seattle)LOC100506098
Human Protein AtlasENSG00000233834
Protein Interaction databases
FunCoupENSG00000233834
BioGRIDLOC100506098
STRING (EMBL)LOC100506098
ZODIACLOC100506098
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506098
BioCentury BCIQLOC100506098
ClinGenLOC100506098
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506098
Clinical trialLOC100506098
Miscellaneous
canSAR (ICR)LOC100506098 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506098
EVEXLOC100506098
GoPubMedLOC100506098
iHOPLOC100506098
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 16:02:30 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.