Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928696 (uncharacterized LOC101928696)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928696
Atlas_Id 67408
Location 1q25.1  [Link to chromosome band 1q25]
Location_base_pair Starts at 174934947 and ends at 174954261 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)LOC101928696  101928696  uncharacterized LOC101928696
Aliases
GeneCards (Weizmann)LOC101928696
Ensembl hg19 (Hinxton)ENSG00000229531 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000229531 [Gene_View]  chr1:174934947-174954261 [Contig_View]  LOC101928696 [Vega]
ICGC DataPortalENSG00000229531
TCGA cBioPortalLOC101928696
AceView (NCBI)LOC101928696
Genatlas (Paris)LOC101928696
WikiGenes101928696
SOURCE (Princeton)LOC101928696
Genetics Home Reference (NIH)LOC101928696
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928696  -     chr1:174934947-174954261 -  1q25.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928696  -     1q25.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101928696 - 1q25.1 [CytoView hg19]  LOC101928696 - 1q25.1 [CytoView hg38]
Mapping of homologs : NCBILOC101928696 [Mapview hg19]  LOC101928696 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI807953 BX102231
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928696
Cluster EST : UnigeneHs.666680 [ NCBI ]
CGAP (NCI)Hs.666680
Alternative Splicing GalleryENSG00000229531
Gene ExpressionLOC101928696 [ NCBI-GEO ]   LOC101928696 [ EBI - ARRAY_EXPRESS ]   LOC101928696 [ SEEK ]   LOC101928696 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928696 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928696
GTEX Portal (Tissue expression)LOC101928696
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928696
DMDM Disease mutations101928696
Blocks (Seattle)LOC101928696
Human Protein AtlasENSG00000229531
Protein Interaction databases
FunCoupENSG00000229531
BioGRIDLOC101928696
STRING (EMBL)LOC101928696
ZODIACLOC101928696
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928696
BioCentury BCIQLOC101928696
ClinGenLOC101928696
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928696
Clinical trialLOC101928696
Miscellaneous
canSAR (ICR)LOC101928696 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928696
EVEXLOC101928696
GoPubMedLOC101928696
iHOPLOC101928696
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 Sep 18 13:21:05 CEST 2017

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