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

LOC100996461 (uncharacterized LOC100996461)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100996461
Atlas_Id 66970
Location 2p13.1  [Link to chromosome band 2p13]
Location_base_pair Starts at 73700429 and ends at 73707560 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100996461  100996461  uncharacterized LOC100996461
Aliases
GeneCards (Weizmann)LOC100996461
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr2:73700429-73707560 [Contig_View]  LOC100996461 [Vega]
TCGA cBioPortalLOC100996461
AceView (NCBI)LOC100996461
Genatlas (Paris)LOC100996461
WikiGenes100996461
SOURCE (Princeton)LOC100996461
Genetics Home Reference (NIH)LOC100996461
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100996461  -     chr2:73700429-73707560 +  2p13.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100996461  -     2p13.1   [Description]    (hg19-Feb_2009)
EnsemblLOC100996461 - 2p13.1 [CytoView hg19]  LOC100996461 - 2p13.1 [CytoView hg38]
Mapping of homologs : NCBILOC100996461 [Mapview hg19]  LOC100996461 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK304146
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100996461
Cluster EST : UnigeneHs.458287 [ NCBI ]
CGAP (NCI)Hs.458287
Gene ExpressionLOC100996461 [ NCBI-GEO ]   LOC100996461 [ EBI - ARRAY_EXPRESS ]   LOC100996461 [ SEEK ]   LOC100996461 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100996461 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100996461
GTEX Portal (Tissue expression)LOC100996461
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100996461
DMDM Disease mutations100996461
Blocks (Seattle)LOC100996461
Protein Interaction databases
BioGRIDLOC100996461
STRING (EMBL)LOC100996461
ZODIACLOC100996461
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100996461
BioCentury BCIQLOC100996461
ClinGenLOC100996461
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100996461
Clinical trialLOC100996461
Miscellaneous
canSAR (ICR)LOC100996461 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100996461
EVEXLOC100996461
GoPubMedLOC100996461
iHOPLOC100996461
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 Nov 21 13:49:20 CET 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.