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LOC100500773 (serine/arginine-rich splicing factor 3 pseudogene)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100500773
Atlas_Id 66735
Location 8q22.1  [Link to chromosome band 8q22]
Location_base_pair Starts at 96959213 and ends at 96960576 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)LOC100500773  100500773  serine/arginine-rich splicing factor 3 pseudogene
Aliases
GeneCards (Weizmann)LOC100500773
Ensembl hg19 (Hinxton) [Gene_View]  chr8:96959213-96960576 [Contig_View]  LOC100500773 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr8:96959213-96960576 [Contig_View]  LOC100500773 [Vega]
TCGA cBioPortalLOC100500773
AceView (NCBI)LOC100500773
Genatlas (Paris)LOC100500773
WikiGenes100500773
SOURCE (Princeton)LOC100500773
Genetics Home Reference (NIH)LOC100500773
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100500773  -     chr8:96959213-96960576 -  8q22.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100500773  -     8q22.1   [Description]    (hg38-Dec_2013)
EnsemblLOC100500773 - 8q22.1 [CytoView hg19]  LOC100500773 - 8q22.1 [CytoView hg38]
Mapping of homologs : NCBILOC100500773 [Mapview hg19]  LOC100500773 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA219048 AA219199 AA572834
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000008 NC_018919 NT_008046 NW_004929340
Consensus coding sequences : CCDS (NCBI)LOC100500773
Cluster EST : UnigeneHs.741582 [ NCBI ]
CGAP (NCI)Hs.741582
Gene ExpressionLOC100500773 [ NCBI-GEO ]   LOC100500773 [ EBI - ARRAY_EXPRESS ]   LOC100500773 [ SEEK ]   LOC100500773 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100500773 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100500773
GTEX Portal (Tissue expression)LOC100500773
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100500773
DMDM Disease mutations100500773
Blocks (Seattle)LOC100500773
Protein Interaction databases
BioGRIDLOC100500773
STRING (EMBL)LOC100500773
ZODIACLOC100500773
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100500773
BioCentury BCIQLOC100500773
ClinGenLOC100500773
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100500773
Clinical trialLOC100500773
Miscellaneous
canSAR (ICR)LOC100500773 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100500773
EVEXLOC100500773
GoPubMedLOC100500773
iHOPLOC100500773
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 12:16:48 CET 2017

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