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

XLOC_007697 (uncharacterized LOC105500239)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105500239
Atlas_Id 76811
Location 9p11.1  [Link to chromosome band 9p11]
Location_base_pair Starts at 42788400 and ends at 42789608 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)XLOC_007697  105500239  uncharacterized LOC105500239
Aliases
GeneCards (Weizmann)XLOC_007697
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr9:42788400-42789608 [Contig_View]  XLOC_007697 [Vega]
TCGA cBioPortalXLOC_007697
AceView (NCBI)XLOC_007697
Genatlas (Paris)XLOC_007697
WikiGenes105500239
SOURCE (Princeton)XLOC_007697
Genetics Home Reference (NIH)XLOC_007697
Genomic and cartography
GoldenPath hg38 (UCSC)XLOC_007697  -     chr9:42788400-42789608 +  9p11.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)XLOC_007697  -     9p11.1   [Description]    (hg19-Feb_2009)
EnsemblXLOC_007697 - 9p11.1 [CytoView hg19]  XLOC_007697 - 9p11.1 [CytoView hg38]
Mapping of homologs : NCBIXLOC_007697 [Mapview hg19]  XLOC_007697 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BG182211
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)XLOC_007697
Gene ExpressionXLOC_007697 [ NCBI-GEO ]   XLOC_007697 [ EBI - ARRAY_EXPRESS ]   XLOC_007697 [ SEEK ]   XLOC_007697 [ MEM ]
Gene Expression Viewer (FireBrowse)XLOC_007697 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105500239
GTEX Portal (Tissue expression)XLOC_007697
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)XLOC_007697
DMDM Disease mutations105500239
Blocks (Seattle)XLOC_007697
Protein Interaction databases
BioGRIDXLOC_007697
STRING (EMBL)XLOC_007697
ZODIACXLOC_007697
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105500239
BioCentury BCIQXLOC_007697
ClinGenXLOC_007697
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105500239
Clinical trialXLOC_007697
Miscellaneous
canSAR (ICR)XLOC_007697 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineXLOC_007697
EVEXXLOC_007697
GoPubMedXLOC_007697
iHOPXLOC_007697
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 13:43:58 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.