Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929199 (uncharacterized LOC101929199)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929199
Atlas_Id 67512
Location 4p15.2  [Link to chromosome band 4p15]
Location_base_pair Starts at 27219101 and ends at 27283847 bp from pter ( according to hg19-Feb_2009)

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)LOC101929199  101929199  uncharacterized LOC101929199
Aliases
GeneCards (Weizmann)LOC101929199
Ensembl hg19 (Hinxton)ENSG00000249699 [Gene_View]  chr4:27219101-27283847 [Contig_View]  LOC101929199 [Vega]
Ensembl hg38 (Hinxton)ENSG00000249699 [Gene_View]  chr4:27219101-27283847 [Contig_View]  LOC101929199 [Vega]
ICGC DataPortalENSG00000249699
TCGA cBioPortalLOC101929199
AceView (NCBI)LOC101929199
Genatlas (Paris)LOC101929199
WikiGenes101929199
SOURCE (Princeton)LOC101929199
Genetics Home Reference (NIH)LOC101929199
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101929199  -     chr4:27219101-27283847 +  4p15.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101929199  -     4p15.2   [Description]    (hg38-Dec_2013)
EnsemblLOC101929199 - 4p15.2 [CytoView hg19]  LOC101929199 - 4p15.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929199 [Mapview hg19]  LOC101929199 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK125145 HG496800
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000004 NC_018915 NT_006316 NW_004929315
Consensus coding sequences : CCDS (NCBI)LOC101929199
Cluster EST : UnigeneHs.570815 [ NCBI ]
CGAP (NCI)Hs.570815
Alternative Splicing GalleryENSG00000249699
Gene ExpressionLOC101929199 [ NCBI-GEO ]   LOC101929199 [ EBI - ARRAY_EXPRESS ]   LOC101929199 [ SEEK ]   LOC101929199 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929199 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929199
GTEX Portal (Tissue expression)LOC101929199
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929199
DMDM Disease mutations101929199
Blocks (Seattle)LOC101929199
Human Protein AtlasENSG00000249699
Protein Interaction databases
FunCoupENSG00000249699
BioGRIDLOC101929199
STRING (EMBL)LOC101929199
ZODIACLOC101929199
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929199
BioCentury BCIQLOC101929199
ClinGenLOC101929199
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929199
Clinical trialLOC101929199
Miscellaneous
canSAR (ICR)LOC101929199 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929199
EVEXLOC101929199
GoPubMedLOC101929199
iHOPLOC101929199
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 Mar 14 12:20:27 CET 2017

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