Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   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

LOC100130698 (uncharacterized LOC100130698)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100130698
Atlas_Id 66420
Location 10q23.1  [Link to chromosome band 10q23]
Location_base_pair Starts at 82009466 and ends at 82013395 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)LOC100130698  100130698  uncharacterized LOC100130698
Aliases
GeneCards (Weizmann)LOC100130698
Ensembl hg19 (Hinxton) [Gene_View]  chr10:82009466-82013395 [Contig_View]  LOC100130698 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr10:82009466-82013395 [Contig_View]  LOC100130698 [Vega]
TCGA cBioPortalLOC100130698
AceView (NCBI)LOC100130698
Genatlas (Paris)LOC100130698
WikiGenes100130698
SOURCE (Princeton)LOC100130698
Genetics Home Reference (NIH)LOC100130698
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100130698  -     chr10:82009466-82013395 +  10q23.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100130698  -     10q23.1   [Description]    (hg38-Dec_2013)
EnsemblLOC100130698 - 10q23.1 [CytoView hg19]  LOC100130698 - 10q23.1 [CytoView hg38]
Mapping of homologs : NCBILOC100130698 [Mapview hg19]  LOC100130698 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK125824 AK128140 DQ574618
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000010 NC_018921 NT_030059 NW_004929376
Consensus coding sequences : CCDS (NCBI)LOC100130698
Cluster EST : UnigeneHs.447456 [ NCBI ]
CGAP (NCI)Hs.447456
Gene ExpressionLOC100130698 [ NCBI-GEO ]   LOC100130698 [ EBI - ARRAY_EXPRESS ]   LOC100130698 [ SEEK ]   LOC100130698 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100130698 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100130698
GTEX Portal (Tissue expression)LOC100130698
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100130698
DMDM Disease mutations100130698
Blocks (Seattle)LOC100130698
IPIIPI00445517   
Protein Interaction databases
BioGRIDLOC100130698
STRING (EMBL)LOC100130698
ZODIACLOC100130698
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100130698
BioCentury BCIQLOC100130698
ClinGenLOC100130698
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100130698
Clinical trialLOC100130698
Miscellaneous
canSAR (ICR)LOC100130698 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100130698
EVEXLOC100130698
GoPubMedLOC100130698
iHOPLOC100130698
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 12:15:38 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.