Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928098 (uncharacterized LOC101928098)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928098
Atlas_Id 76745
Location 1p21.3  [Link to chromosome band 1p21]
Location_base_pair Starts at 95061596 and ends at 95067545 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)LOC101928098  101928098  uncharacterized LOC101928098
Aliases
GeneCards (Weizmann)LOC101928098
Ensembl hg19 (Hinxton)ENSG00000230427 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000230427 [Gene_View]  chr1:95061596-95067545 [Contig_View]  LOC101928098 [Vega]
ICGC DataPortalENSG00000230427
TCGA cBioPortalLOC101928098
AceView (NCBI)LOC101928098
Genatlas (Paris)LOC101928098
WikiGenes101928098
SOURCE (Princeton)LOC101928098
Genetics Home Reference (NIH)LOC101928098
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928098  -     chr1:95061596-95067545 +  1p21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928098  -     1p21.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101928098 - 1p21.3 [CytoView hg19]  LOC101928098 - 1p21.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928098 [Mapview hg19]  LOC101928098 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC040907 BG193554
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928098
Cluster EST : UnigeneHs.730090 [ NCBI ]
CGAP (NCI)Hs.730090
Alternative Splicing GalleryENSG00000230427
Gene ExpressionLOC101928098 [ NCBI-GEO ]   LOC101928098 [ EBI - ARRAY_EXPRESS ]   LOC101928098 [ SEEK ]   LOC101928098 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928098 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928098
GTEX Portal (Tissue expression)LOC101928098
Human Protein AtlasENSG00000230427-LOC101928098 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928098
DMDM Disease mutations101928098
Blocks (Seattle)LOC101928098
Human Protein Atlas [tissue]ENSG00000230427-LOC101928098 [tissue]
Protein Interaction databases
FunCoupENSG00000230427
BioGRIDLOC101928098
STRING (EMBL)LOC101928098
ZODIACLOC101928098
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928098
BioCentury BCIQLOC101928098
ClinGenLOC101928098
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928098
Clinical trialLOC101928098
Miscellaneous
canSAR (ICR)LOC101928098 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928098
EVEXLOC101928098
GoPubMedLOC101928098
iHOPLOC101928098
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Nov 20 19:47:10 CET 2017

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