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LOC101929134 (uncharacterized LOC101929134)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929134
Atlas_Id 78071
Location 4q22.1  [Link to chromosome band 4q22]
Location_base_pair Starts at 88523810 and ends at 88524996 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

Entrez_Gene (NCBI)
Nomenclature
HGNC (Hugo)-   -
Cards
LOC101929134  101929134  uncharacterized LOC101929134
Aliases
GeneCards (Weizmann)LOC101929134
Ensembl hg19 (Hinxton)ENSG00000138641 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000138641 [Gene_View]  chr4:88523810-88524996 [Contig_View]  LOC101929134 [Vega]
ICGC DataPortalENSG00000138641
TCGA cBioPortalLOC101929134
AceView (NCBI)LOC101929134
Genatlas (Paris)LOC101929134
WikiGenes101929134
SOURCE (Princeton)LOC101929134
Genetics Home Reference (NIH)LOC101929134
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929134  -     chr4:88523810-88524996 +  4q22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929134  -     4q22.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929134 - 4q22.1 [CytoView hg19]  LOC101929134 - 4q22.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929134 [Mapview hg19]  LOC101929134 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BP199952 BX106511 CD104988
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929134
Cluster EST : UnigeneHs.734064 [ NCBI ]
CGAP (NCI)Hs.734064
Alternative Splicing GalleryENSG00000138641
Gene ExpressionLOC101929134 [ NCBI-GEO ]   LOC101929134 [ EBI - ARRAY_EXPRESS ]   LOC101929134 [ SEEK ]   LOC101929134 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929134 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929134
GTEX Portal (Tissue expression)LOC101929134
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929134
DMDM Disease mutations101929134
Blocks (Seattle)LOC101929134
Human Protein AtlasENSG00000138641
Protein Interaction databases
FunCoupENSG00000138641
BioGRIDLOC101929134
STRING (EMBL)LOC101929134
ZODIACLOC101929134
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929134
BioCentury BCIQLOC101929134
ClinGenLOC101929134
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929134
Clinical trialLOC101929134
Miscellaneous
canSAR (ICR)LOC101929134 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929134
EVEXLOC101929134
GoPubMedLOC101929134
iHOPLOC101929134
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 13:21:28 CEST 2017

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