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LOC101928168 (uncharacterized LOC101928168)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928168
Atlas_Id 67297
Location 7p14.3  [Link to chromosome band 7p14]
Location_base_pair Starts at 29125033 and ends at 29128172 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)LOC101928168  101928168  uncharacterized LOC101928168
Aliases
GeneCards (Weizmann)LOC101928168
Ensembl hg19 (Hinxton)ENSG00000106069 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000106069 [Gene_View]  chr7:29125033-29128172 [Contig_View]  LOC101928168 [Vega]
ICGC DataPortalENSG00000106069
TCGA cBioPortalLOC101928168
AceView (NCBI)LOC101928168
Genatlas (Paris)LOC101928168
WikiGenes101928168
SOURCE (Princeton)LOC101928168
Genetics Home Reference (NIH)LOC101928168
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928168  -     chr7:29125033-29128172 +  7p14.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928168  -     7p14.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101928168 - 7p14.3 [CytoView hg19]  LOC101928168 - 7p14.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928168 [Mapview hg19]  LOC101928168 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX116694 DA098992
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928168
Cluster EST : UnigeneHs.666750 [ NCBI ]
CGAP (NCI)Hs.666750
Alternative Splicing GalleryENSG00000106069
Gene ExpressionLOC101928168 [ NCBI-GEO ]   LOC101928168 [ EBI - ARRAY_EXPRESS ]   LOC101928168 [ SEEK ]   LOC101928168 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928168 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928168
GTEX Portal (Tissue expression)LOC101928168
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928168
DMDM Disease mutations101928168
Blocks (Seattle)LOC101928168
Human Protein AtlasENSG00000106069
Protein Interaction databases
FunCoupENSG00000106069
BioGRIDLOC101928168
STRING (EMBL)LOC101928168
ZODIACLOC101928168
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928168
BioCentury BCIQLOC101928168
ClinGenLOC101928168
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928168
Clinical trialLOC101928168
Miscellaneous
canSAR (ICR)LOC101928168 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928168
EVEXLOC101928168
GoPubMedLOC101928168
iHOPLOC101928168
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 : Wed Jun 7 16:04:59 CEST 2017

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