Atlas of Genetics and Cytogenetics in Oncology and Haematology

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LOC102467222 (uncharacterized LOC102467222)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 102467222
Atlas_Id 76530
Location 8p21.3  [Link to chromosome band 8p21]
Location_base_pair Starts at 20953633 and ends at 20968938 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

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC102467222  102467222  uncharacterized LOC102467222
Aliases
GeneCards (Weizmann)LOC102467222
Ensembl hg19 (Hinxton)ENSG00000253147 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000253147 [Gene_View]  ENSG00000253147 [Sequence]  chr8:20953633-20968938 [Contig_View]  LOC102467222 [Vega]
ICGC DataPortalENSG00000253147
TCGA cBioPortalLOC102467222
AceView (NCBI)LOC102467222
Genatlas (Paris)LOC102467222
WikiGenes102467222
SOURCE (Princeton)LOC102467222
Genetics Home Reference (NIH)LOC102467222
Genomic and cartography
GoldenPath hg38 (UCSC)LOC102467222  -     chr8:20953633-20968938 +  8p21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC102467222  -     8p21.3   [Description]    (hg19-Feb_2009)
GoldenPathLOC102467222 - 8p21.3 [CytoView hg19]  LOC102467222 - 8p21.3 [CytoView hg38]
ImmunoBaseENSG00000253147
Mapping of homologs : NCBILOC102467222 [Mapview hg19]  LOC102467222 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX101391 HY012906 HY197102
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC102467222
Cluster EST : UnigeneHs.444226 [ NCBI ]
CGAP (NCI)Hs.444226
Alternative Splicing GalleryENSG00000253147
Gene ExpressionLOC102467222 [ NCBI-GEO ]   LOC102467222 [ EBI - ARRAY_EXPRESS ]   LOC102467222 [ SEEK ]   LOC102467222 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC102467222 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102467222
GTEX Portal (Tissue expression)LOC102467222
Human Protein AtlasENSG00000253147-LOC102467222 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC102467222
DMDM Disease mutations102467222
Blocks (Seattle)LOC102467222
Human Protein Atlas [tissue]ENSG00000253147-LOC102467222 [tissue]
Protein Interaction databases
FunCoupENSG00000253147
BioGRIDLOC102467222
STRING (EMBL)LOC102467222
ZODIACLOC102467222
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease102467222
BioCentury BCIQLOC102467222
ClinGenLOC102467222
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102467222
Clinical trialLOC102467222
Miscellaneous
canSAR (ICR)LOC102467222 (select the gene name)
DataMed IndexLOC102467222
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC102467222
EVEXLOC102467222
GoPubMedLOC102467222
iHOPLOC102467222
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 Sep 3 15:45:24 CEST 2019
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