Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928700 (uncharacterized LOC101928700)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928700
Atlas_Id 67410
Location 7q35  [Link to chromosome band 7q35]
Location_base_pair Starts at 147080938 and ends at 147097609 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)LOC101928700  101928700  uncharacterized LOC101928700
Aliases
GeneCards (Weizmann)LOC101928700
Ensembl hg19 (Hinxton)ENSG00000236795 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000236795 [Gene_View]  chr7:147080938-147097609 [Contig_View]  LOC101928700 [Vega]
ICGC DataPortalENSG00000236795
TCGA cBioPortalLOC101928700
AceView (NCBI)LOC101928700
Genatlas (Paris)LOC101928700
WikiGenes101928700
SOURCE (Princeton)LOC101928700
Genetics Home Reference (NIH)LOC101928700
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928700  -     chr7:147080938-147097609 -  7q35   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928700  -     7q35   [Description]    (hg19-Feb_2009)
EnsemblLOC101928700 - 7q35 [CytoView hg19]  LOC101928700 - 7q35 [CytoView hg38]
Mapping of homologs : NCBILOC101928700 [Mapview hg19]  LOC101928700 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC026117
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928700
Cluster EST : UnigeneHs.571218 [ NCBI ]
CGAP (NCI)Hs.571218
Alternative Splicing GalleryENSG00000236795
Gene ExpressionLOC101928700 [ NCBI-GEO ]   LOC101928700 [ EBI - ARRAY_EXPRESS ]   LOC101928700 [ SEEK ]   LOC101928700 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928700 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928700
GTEX Portal (Tissue expression)LOC101928700
Human Protein AtlasENSG00000236795-LOC101928700 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928700
DMDM Disease mutations101928700
Blocks (Seattle)LOC101928700
Human Protein Atlas [tissue]ENSG00000236795-LOC101928700 [tissue]
Protein Interaction databases
FunCoupENSG00000236795
BioGRIDLOC101928700
STRING (EMBL)LOC101928700
ZODIACLOC101928700
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928700
BioCentury BCIQLOC101928700
ClinGenLOC101928700
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928700
Clinical trialLOC101928700
Miscellaneous
canSAR (ICR)LOC101928700 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928700
EVEXLOC101928700
GoPubMedLOC101928700
iHOPLOC101928700
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 Nov 20 19:47:51 CET 2017

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