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

LOC100132147 (uncharacterized LOC100132147)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100132147
Atlas_Id 66537
Location 1p36.13  [Link to chromosome band 1p36]
Location_base_pair Starts at 16860385 and ends at 16862144 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)LOC100132147  100132147  uncharacterized LOC100132147
Aliases
GeneCards (Weizmann)LOC100132147
Ensembl hg19 (Hinxton) [Gene_View]  chr1:16860385-16862144 [Contig_View]  LOC100132147 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr1:16860385-16862144 [Contig_View]  LOC100132147 [Vega]
TCGA cBioPortalLOC100132147
AceView (NCBI)LOC100132147
Genatlas (Paris)LOC100132147
WikiGenes100132147
SOURCE (Princeton)LOC100132147
Genetics Home Reference (NIH)LOC100132147
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100132147  -     chr1:16860385-16862144 -  1p36.13   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100132147  -     1p36.13   [Description]    (hg38-Dec_2013)
EnsemblLOC100132147 - 1p36.13 [CytoView hg19]  LOC100132147 - 1p36.13 [CytoView hg38]
Mapping of homologs : NCBILOC100132147 [Mapview hg19]  LOC100132147 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC036435 BC126340
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_004610 NW_001841815 NW_004929289
Consensus coding sequences : CCDS (NCBI)LOC100132147
Cluster EST : UnigeneHs.722379 [ NCBI ]
CGAP (NCI)Hs.722379
Gene ExpressionLOC100132147 [ NCBI-GEO ]   LOC100132147 [ EBI - ARRAY_EXPRESS ]   LOC100132147 [ SEEK ]   LOC100132147 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100132147 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100132147
GTEX Portal (Tissue expression)LOC100132147
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100132147
DMDM Disease mutations100132147
Blocks (Seattle)LOC100132147
IPIIPI00847224   
Protein Interaction databases
BioGRIDLOC100132147
STRING (EMBL)LOC100132147
ZODIACLOC100132147
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100132147
BioCentury BCIQLOC100132147
ClinGenLOC100132147
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100132147
Clinical trialLOC100132147
Miscellaneous
canSAR (ICR)LOC100132147 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100132147
EVEXLOC100132147
GoPubMedLOC100132147
iHOPLOC100132147
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 12:16:03 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.