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

LOC101927339 (uncharacterized LOC101927339)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927339
Atlas_Id 76588
Location 17q12  [Link to chromosome band 17q12]
Location_base_pair Starts at 34312626 and ends at 34317306 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)LOC101927339  101927339  uncharacterized LOC101927339
Aliases
GeneCards (Weizmann)LOC101927339
Ensembl hg19 (Hinxton) [Gene_View]  chr17:34312626-34317306 [Contig_View]  LOC101927339 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr17:34312626-34317306 [Contig_View]  LOC101927339 [Vega]
TCGA cBioPortalLOC101927339
AceView (NCBI)LOC101927339
Genatlas (Paris)LOC101927339
WikiGenes101927339
SOURCE (Princeton)LOC101927339
Genetics Home Reference (NIH)LOC101927339
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101927339  -     chr17:34312626-34317306 +  17q12   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101927339  -     17q12   [Description]    (hg38-Dec_2013)
EnsemblLOC101927339 - 17q12 [CytoView hg19]  LOC101927339 - 17q12 [CytoView hg38]
Mapping of homologs : NCBILOC101927339 [Mapview hg19]  LOC101927339 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC028693 BC070118 LN608647
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000017 NC_018928 NT_010783 NT_187614 NW_004929407
Consensus coding sequences : CCDS (NCBI)LOC101927339
Cluster EST : UnigeneHs.569800 [ NCBI ]
CGAP (NCI)Hs.569800
Gene ExpressionLOC101927339 [ NCBI-GEO ]   LOC101927339 [ EBI - ARRAY_EXPRESS ]   LOC101927339 [ SEEK ]   LOC101927339 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927339 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927339
GTEX Portal (Tissue expression)LOC101927339
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927339
DMDM Disease mutations101927339
Blocks (Seattle)LOC101927339
Protein Interaction databases
BioGRIDLOC101927339
STRING (EMBL)LOC101927339
ZODIACLOC101927339
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927339
BioCentury BCIQLOC101927339
ClinGenLOC101927339
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927339
Clinical trialLOC101927339
Miscellaneous
canSAR (ICR)LOC101927339 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927339
EVEXLOC101927339
GoPubMedLOC101927339
iHOPLOC101927339
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 12:18:25 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.