Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100996351 (uncharacterized LOC100996351)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100996351
Atlas_Id 66965
Location 19p13.3  [Link to chromosome band 19p13]
Location_base_pair Starts at 3141574 and ends at 3155173 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)LOC100996351  100996351  uncharacterized LOC100996351
Aliases
GeneCards (Weizmann)LOC100996351
Ensembl hg19 (Hinxton)ENSG00000267551 [Gene_View]  chr19:3141574-3155173 [Contig_View]  LOC100996351 [Vega]
Ensembl hg38 (Hinxton)ENSG00000267551 [Gene_View]  chr19:3141574-3155173 [Contig_View]  LOC100996351 [Vega]
ICGC DataPortalENSG00000267551
TCGA cBioPortalLOC100996351
AceView (NCBI)LOC100996351
Genatlas (Paris)LOC100996351
WikiGenes100996351
SOURCE (Princeton)LOC100996351
Genetics Home Reference (NIH)LOC100996351
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100996351  -     chr19:3141574-3155173 -  19p13.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100996351  -     19p13.3   [Description]    (hg38-Dec_2013)
EnsemblLOC100996351 - 19p13.3 [CytoView hg19]  LOC100996351 - 19p13.3 [CytoView hg38]
Mapping of homologs : NCBILOC100996351 [Mapview hg19]  LOC100996351 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK123032 HG510252
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011295 NW_004929412
Consensus coding sequences : CCDS (NCBI)LOC100996351
Alternative Splicing GalleryENSG00000267551
Gene ExpressionLOC100996351 [ NCBI-GEO ]   LOC100996351 [ EBI - ARRAY_EXPRESS ]   LOC100996351 [ SEEK ]   LOC100996351 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100996351 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100996351
GTEX Portal (Tissue expression)LOC100996351
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100996351
DMDM Disease mutations100996351
Blocks (Seattle)LOC100996351
Human Protein AtlasENSG00000267551
Protein Interaction databases
FunCoupENSG00000267551
BioGRIDLOC100996351
STRING (EMBL)LOC100996351
ZODIACLOC100996351
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100996351
BioCentury BCIQLOC100996351
ClinGenLOC100996351
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100996351
Clinical trialLOC100996351
Miscellaneous
canSAR (ICR)LOC100996351 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100996351
EVEXLOC100996351
GoPubMedLOC100996351
iHOPLOC100996351
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 12:17:45 CET 2017

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