Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927636 (uncharacterized LOC101927636)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927636
Atlas_Id 67182
Location 4q31.21  [Link to chromosome band 4q31]
Location_base_pair Starts at 143912331 and ends at 143982452 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)LOC101927636  101927636  uncharacterized LOC101927636
Aliases
GeneCards (Weizmann)LOC101927636
Ensembl hg19 (Hinxton)ENSG00000251600 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000251600 [Gene_View]  chr4:143912331-143982452 [Contig_View]  LOC101927636 [Vega]
ICGC DataPortalENSG00000251600
TCGA cBioPortalLOC101927636
AceView (NCBI)LOC101927636
Genatlas (Paris)LOC101927636
WikiGenes101927636
SOURCE (Princeton)LOC101927636
Genetics Home Reference (NIH)LOC101927636
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927636  -     chr4:143912331-143982452 +  4q31.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927636  -     4q31.21   [Description]    (hg19-Feb_2009)
EnsemblLOC101927636 - 4q31.21 [CytoView hg19]  LOC101927636 - 4q31.21 [CytoView hg38]
Mapping of homologs : NCBILOC101927636 [Mapview hg19]  LOC101927636 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC029578
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927636
Cluster EST : UnigeneHs.658686 [ NCBI ]
CGAP (NCI)Hs.658686
Alternative Splicing GalleryENSG00000251600
Gene ExpressionLOC101927636 [ NCBI-GEO ]   LOC101927636 [ EBI - ARRAY_EXPRESS ]   LOC101927636 [ SEEK ]   LOC101927636 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927636 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927636
GTEX Portal (Tissue expression)LOC101927636
Human Protein AtlasENSG00000251600-LOC101927636 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927636
DMDM Disease mutations101927636
Blocks (Seattle)LOC101927636
Human Protein Atlas [tissue]ENSG00000251600-LOC101927636 [tissue]
Protein Interaction databases
FunCoupENSG00000251600
BioGRIDLOC101927636
STRING (EMBL)LOC101927636
ZODIACLOC101927636
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927636
BioCentury BCIQLOC101927636
ClinGenLOC101927636
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927636
Clinical trialLOC101927636
Miscellaneous
canSAR (ICR)LOC101927636 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927636
EVEXLOC101927636
GoPubMedLOC101927636
iHOPLOC101927636
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 Nov 21 13:50:18 CET 2017

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