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

LOC101927139 (uncharacterized LOC101927139)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927139
Atlas_Id 67064
Location 1p31.3  [Link to chromosome band 1p31]
Location_base_pair Starts at 66042500 and ends at 66050718 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)LOC101927139  101927139  uncharacterized LOC101927139
Aliases
GeneCards (Weizmann)LOC101927139
Ensembl hg19 (Hinxton)ENSG00000227466 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000227466 [Gene_View]  chr1:66042500-66050718 [Contig_View]  LOC101927139 [Vega]
ICGC DataPortalENSG00000227466
TCGA cBioPortalLOC101927139
AceView (NCBI)LOC101927139
Genatlas (Paris)LOC101927139
WikiGenes101927139
SOURCE (Princeton)LOC101927139
Genetics Home Reference (NIH)LOC101927139
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927139  -     chr1:66042500-66050718 -  1p31.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927139  -     1p31.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101927139 - 1p31.3 [CytoView hg19]  LOC101927139 - 1p31.3 [CytoView hg38]
Mapping of homologs : NCBILOC101927139 [Mapview hg19]  LOC101927139 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX109047
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927139
Cluster EST : UnigeneHs.127908 [ NCBI ]
CGAP (NCI)Hs.127908
Alternative Splicing GalleryENSG00000227466
Gene ExpressionLOC101927139 [ NCBI-GEO ]   LOC101927139 [ EBI - ARRAY_EXPRESS ]   LOC101927139 [ SEEK ]   LOC101927139 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927139 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927139
GTEX Portal (Tissue expression)LOC101927139
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927139
DMDM Disease mutations101927139
Blocks (Seattle)LOC101927139
Human Protein AtlasENSG00000227466
Protein Interaction databases
FunCoupENSG00000227466
BioGRIDLOC101927139
STRING (EMBL)LOC101927139
ZODIACLOC101927139
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927139
BioCentury BCIQLOC101927139
ClinGenLOC101927139
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927139
Clinical trialLOC101927139
Miscellaneous
canSAR (ICR)LOC101927139 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927139
EVEXLOC101927139
GoPubMedLOC101927139
iHOPLOC101927139
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 13:19:44 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.