Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928372 (uncharacterized LOC101928372)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928372
Atlas_Id 67340
Location 1q23.3  [Link to chromosome band 1q23]
Location_base_pair Starts at 160932465 and ends at 160949922 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)LOC101928372  101928372  uncharacterized LOC101928372
Aliases
GeneCards (Weizmann)LOC101928372
Ensembl hg19 (Hinxton)ENSG00000198358 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000198358 [Gene_View]  chr1:160932465-160949922 [Contig_View]  LOC101928372 [Vega]
ICGC DataPortalENSG00000198358
TCGA cBioPortalLOC101928372
AceView (NCBI)LOC101928372
Genatlas (Paris)LOC101928372
WikiGenes101928372
SOURCE (Princeton)LOC101928372
Genetics Home Reference (NIH)LOC101928372
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928372  -     chr1:160932465-160949922 +  1q23.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928372  -     1q23.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101928372 - 1q23.3 [CytoView hg19]  LOC101928372 - 1q23.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928372 [Mapview hg19]  LOC101928372 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC035240
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928372
Alternative Splicing GalleryENSG00000198358
Gene ExpressionLOC101928372 [ NCBI-GEO ]   LOC101928372 [ EBI - ARRAY_EXPRESS ]   LOC101928372 [ SEEK ]   LOC101928372 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928372 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928372
GTEX Portal (Tissue expression)LOC101928372
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928372
DMDM Disease mutations101928372
Blocks (Seattle)LOC101928372
Human Protein AtlasENSG00000198358
Protein Interaction databases
FunCoupENSG00000198358
BioGRIDLOC101928372
STRING (EMBL)LOC101928372
ZODIACLOC101928372
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928372
BioCentury BCIQLOC101928372
ClinGenLOC101928372
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928372
Clinical trialLOC101928372
Miscellaneous
canSAR (ICR)LOC101928372 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928372
EVEXLOC101928372
GoPubMedLOC101928372
iHOPLOC101928372
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 Sep 18 13:20:49 CEST 2017

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