Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC104968399 (uncharacterized LOC104968399)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 104968399
Atlas_Id 77351
Location 18p11.31  [Link to chromosome band 18p11]
Location_base_pair Starts at 3255437 and ends at 3261830 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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

Gene Expression Viewer (FireBrowse)
Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC104968399  104968399  uncharacterized LOC104968399
Aliases
GeneCards (Weizmann)LOC104968399
Ensembl hg19 (Hinxton)ENSG00000264235 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264235 [Gene_View]  chr18:3255437-3261830 [Contig_View]  LOC104968399 [Vega]
ICGC DataPortalENSG00000264235
TCGA cBioPortalLOC104968399
AceView (NCBI)LOC104968399
Genatlas (Paris)LOC104968399
WikiGenes104968399
SOURCE (Princeton)LOC104968399
Genetics Home Reference (NIH)LOC104968399
Genomic and cartography
GoldenPath hg38 (UCSC)LOC104968399  -     chr18:3255437-3261830 -  18p11.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC104968399  -     18p11.31   [Description]    (hg19-Feb_2009)
EnsemblLOC104968399 - 18p11.31 [CytoView hg19]  LOC104968399 - 18p11.31 [CytoView hg38]
Mapping of homologs : NCBILOC104968399 [Mapview hg19]  LOC104968399 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AL550084 AV760872 BG201476 BG218162 BG721448
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC104968399
Cluster EST : UnigeneHs.569882 [ NCBI ]
CGAP (NCI)Hs.569882
Alternative Splicing GalleryENSG00000264235
Gene ExpressionLOC104968399 [ NCBI-GEO ]   LOC104968399 [ EBI - ARRAY_EXPRESS ]   LOC104968399 [ SEEK ]   LOC104968399 [ MEM ]
LOC104968399 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)104968399
GTEX Portal (Tissue expression)LOC104968399
Human Protein AtlasENSG00000264235-LOC104968399 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC104968399
DMDM Disease mutations104968399
Blocks (Seattle)LOC104968399
Human Protein Atlas [tissue]ENSG00000264235-LOC104968399 [tissue]
Protein Interaction databases
FunCoupENSG00000264235
BioGRIDLOC104968399
STRING (EMBL)LOC104968399
ZODIACLOC104968399
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease104968399
BioCentury BCIQLOC104968399
ClinGenLOC104968399
Clinical trials, drugs, therapy
html#CTD TARGET=CTD>Chemical/Protein Interactions : CTD104968399
Clinical trialLOC104968399
Miscellaneous
canSAR (ICR)LOC104968399 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC104968399
EVEXLOC104968399
GoPubMedLOC104968399
iHOPLOC104968399
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 Nov 21 13:53:23 CET 2017

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