Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

FAM226B (family with sequence similarity 226 member B (non-protein coding))

Identity

Alias_namesCXorf50B
NCRNA00246B
LINC00246B
chromosome X open reading frame 50B
non-protein coding RNA 246B
long intergenic non-protein coding RNA 246B
family with sequence similarity 226, member B (non-protein coding)
Other alias
HGNC (Hugo) FAM226B
LocusID (NCBI) 653687
Atlas_Id 63164
Location Xq13.1  [Link to chromosome band Xq13]
Location_base_pair Starts at 72777073 and ends at 72779095 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)FAM226B   31964
Cards
Entrez_Gene (NCBI)FAM226B  653687  family with sequence similarity 226 member B (non-protein coding)
AliasesCXorf50B; LINC00246B; NCRNA00246B
GeneCards (Weizmann)FAM226B
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chrX:72777073-72779095 [Contig_View]  FAM226B [Vega]
TCGA cBioPortalFAM226B
AceView (NCBI)FAM226B
Genatlas (Paris)FAM226B
WikiGenes653687
SOURCE (Princeton)FAM226B
Genetics Home Reference (NIH)FAM226B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM226B  -     chrX:72777073-72779095 +  Xq13.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM226B  -     Xq13.1   [Description]    (hg19-Feb_2009)
EnsemblFAM226B - Xq13.1 [CytoView hg19]  FAM226B - Xq13.1 [CytoView hg38]
Mapping of homologs : NCBIFAM226B [Mapview hg19]  FAM226B [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC025725 BC041962 DB480960
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM226B
Cluster EST : UnigeneHs.676982 [ NCBI ]
CGAP (NCI)Hs.676982
Gene ExpressionFAM226B [ NCBI-GEO ]   FAM226B [ EBI - ARRAY_EXPRESS ]   FAM226B [ SEEK ]   FAM226B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM226B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)653687
GTEX Portal (Tissue expression)FAM226B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM226B
DMDM Disease mutations653687
Blocks (Seattle)FAM226B
Protein Interaction databases
BioGRIDFAM226B
STRING (EMBL)FAM226B
ZODIACFAM226B
Ontologies - Pathways
Huge Navigator FAM226B [HugePedia]
snp3D : Map Gene to Disease653687
BioCentury BCIQFAM226B
ClinGenFAM226B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD653687
Chemical/Pharm GKB GenePA165757326
Clinical trialFAM226B
Miscellaneous
canSAR (ICR)FAM226B (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM226B
EVEXFAM226B
GoPubMedFAM226B
iHOPFAM226B
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 : Thu Nov 9 11:46:59 CET 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.