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LOC100507334 (two pore channel 3 pseudogene)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100507334
Atlas_Id 66889
Location 2q13  [Link to chromosome band 2q13]
Location_base_pair Starts at 110245638 and ends at 110266558 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

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100507334  100507334  two pore channel 3 pseudogene
Aliases
GeneCards (Weizmann)LOC100507334
Ensembl hg19 (Hinxton)ENSG00000261760 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261760 [Gene_View]  chr2:110245638-110266558 [Contig_View]  LOC100507334 [Vega]
ICGC DataPortalENSG00000261760
TCGA cBioPortalLOC100507334
AceView (NCBI)LOC100507334
Genatlas (Paris)LOC100507334
WikiGenes100507334
SOURCE (Princeton)LOC100507334
Genetics Home Reference (NIH)LOC100507334
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100507334  -     chr2:110245638-110266558 +  2q13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100507334  -     2q13   [Description]    (hg19-Feb_2009)
EnsemblLOC100507334 - 2q13 [CytoView hg19]  LOC100507334 - 2q13 [CytoView hg38]
Mapping of homologs : NCBILOC100507334 [Mapview hg19]  LOC100507334 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC022085 BC033980 BC042849
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100507334
Cluster EST : UnigeneHs.721040 [ NCBI ]
CGAP (NCI)Hs.721040
Alternative Splicing GalleryENSG00000261760
Gene ExpressionLOC100507334 [ NCBI-GEO ]   LOC100507334 [ EBI - ARRAY_EXPRESS ]   LOC100507334 [ SEEK ]   LOC100507334 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100507334 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507334
GTEX Portal (Tissue expression)LOC100507334
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100507334
DMDM Disease mutations100507334
Blocks (Seattle)LOC100507334
Human Protein AtlasENSG00000261760
Protein Interaction databases
FunCoupENSG00000261760
BioGRIDLOC100507334
STRING (EMBL)LOC100507334
ZODIACLOC100507334
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100507334
BioCentury BCIQLOC100507334
ClinGenLOC100507334
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507334
Clinical trialLOC100507334
Miscellaneous
canSAR (ICR)LOC100507334 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100507334
EVEXLOC100507334
GoPubMedLOC100507334
iHOPLOC100507334
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 13:19:07 CEST 2017

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