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

LOC100506459 (uncharacterized LOC100506459)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506459
Atlas_Id 66819
Location 1p13.1  [Link to chromosome band 1p13]
Location_base_pair Starts at 117035645 and ends at 117041834 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)LOC100506459  100506459  uncharacterized LOC100506459
Aliases
GeneCards (Weizmann)LOC100506459
Ensembl hg19 (Hinxton) [Gene_View]  chr1:117035645-117041834 [Contig_View]  LOC100506459 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr1:117035645-117041834 [Contig_View]  LOC100506459 [Vega]
TCGA cBioPortalLOC100506459
AceView (NCBI)LOC100506459
Genatlas (Paris)LOC100506459
WikiGenes100506459
SOURCE (Princeton)LOC100506459
Genetics Home Reference (NIH)LOC100506459
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100506459  -     chr1:117035645-117041834 -  1p13.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100506459  -     1p13.1   [Description]    (hg38-Dec_2013)
EnsemblLOC100506459 - 1p13.1 [CytoView hg19]  LOC100506459 - 1p13.1 [CytoView hg38]
Mapping of homologs : NCBILOC100506459 [Mapview hg19]  LOC100506459 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK126833 AL832882
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)AC_000133 NC_000001 NC_018912 NT_032977 NW_001838594 NW_004077990
Consensus coding sequences : CCDS (NCBI)LOC100506459
Cluster EST : UnigeneHs.734297 [ NCBI ]
CGAP (NCI)Hs.734297
Gene ExpressionLOC100506459 [ NCBI-GEO ]   LOC100506459 [ EBI - ARRAY_EXPRESS ]   LOC100506459 [ SEEK ]   LOC100506459 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506459 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506459
GTEX Portal (Tissue expression)LOC100506459
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506459
DMDM Disease mutations100506459
Blocks (Seattle)LOC100506459
Protein Interaction databases
BioGRIDLOC100506459
STRING (EMBL)LOC100506459
ZODIACLOC100506459
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506459
BioCentury BCIQLOC100506459
ClinGenLOC100506459
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506459
Clinical trialLOC100506459
Miscellaneous
canSAR (ICR)LOC100506459 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506459
EVEXLOC100506459
GoPubMedLOC100506459
iHOPLOC100506459
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 12:17:09 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.