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

LOC101928000 (uncharacterized LOC101928000)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928000
Atlas_Id 78508
Location 17p13.2  [Link to chromosome band 17p13]
Location_base_pair Starts at 5111935 and ends at 5114382 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)LOC101928000  101928000  uncharacterized LOC101928000
Aliases
GeneCards (Weizmann)LOC101928000
Ensembl hg19 (Hinxton)ENSG00000234327 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000234327 [Gene_View]  chr17:5111935-5114382 [Contig_View]  LOC101928000 [Vega]
ICGC DataPortalENSG00000234327
TCGA cBioPortalLOC101928000
AceView (NCBI)LOC101928000
Genatlas (Paris)LOC101928000
WikiGenes101928000
SOURCE (Princeton)LOC101928000
Genetics Home Reference (NIH)LOC101928000
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928000  -     chr17:5111935-5114382 +  17p13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928000  -     17p13.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101928000 - 17p13.2 [CytoView hg19]  LOC101928000 - 17p13.2 [CytoView hg38]
Mapping of homologs : NCBILOC101928000 [Mapview hg19]  LOC101928000 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BQ066256 BU861115 BX096293
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928000
Cluster EST : UnigeneHs.660048 [ NCBI ]
CGAP (NCI)Hs.660048
Alternative Splicing GalleryENSG00000234327
Gene ExpressionLOC101928000 [ NCBI-GEO ]   LOC101928000 [ EBI - ARRAY_EXPRESS ]   LOC101928000 [ SEEK ]   LOC101928000 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928000 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928000
GTEX Portal (Tissue expression)LOC101928000
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928000
DMDM Disease mutations101928000
Blocks (Seattle)LOC101928000
Human Protein AtlasENSG00000234327
Protein Interaction databases
FunCoupENSG00000234327
BioGRIDLOC101928000
STRING (EMBL)LOC101928000
ZODIACLOC101928000
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928000
BioCentury BCIQLOC101928000
ClinGenLOC101928000
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928000
Clinical trialLOC101928000
Miscellaneous
canSAR (ICR)LOC101928000 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928000
EVEXLOC101928000
GoPubMedLOC101928000
iHOPLOC101928000
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 13:20:29 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.