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

FAM156B (family with sequence similarity 156 member B)

Identity

Alias (NCBI)TMEM29B
HGNC (Hugo) FAM156B
HGNC Previous nameTMEM29B
HGNC Previous nametransmembrane protein 29B
 family with sequence similarity 156, member B
LocusID (NCBI) 727866
Atlas_Id 63047
Location Xp11.22  [Link to chromosome band Xp11]
Location_base_pair Starts at 52898155 and ends at 52908558 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)
MRPL22 (5q33.2) / FAM156B (Xp11.22)PCGF3 (4p16.3) / FAM156B (Xp11.22)RBM14-RBM4 (11q13.2) / FAM156B (Xp11.22)

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)FAM156B   31962
Cards
Entrez_Gene (NCBI)FAM156B    family with sequence similarity 156 member B
AliasesTMEM29B
GeneCards (Weizmann)FAM156B
Ensembl hg19 (Hinxton)ENSG00000179304 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000179304 [Gene_View]  ENSG00000179304 [Sequence]  chrX:52898155-52908558 [Contig_View]  FAM156B [Vega]
ICGC DataPortalENSG00000179304
TCGA cBioPortalFAM156B
AceView (NCBI)FAM156B
Genatlas (Paris)FAM156B
SOURCE (Princeton)FAM156B
Genetics Home Reference (NIH)FAM156B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM156B  -     chrX:52898155-52908558 +  Xp11.22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM156B  -     Xp11.22   [Description]    (hg19-Feb_2009)
GoldenPathFAM156B - Xp11.22 [CytoView hg19]  FAM156B - Xp11.22 [CytoView hg38]
ImmunoBaseENSG00000179304
Genome Data Viewer NCBIFAM156B [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK091598 BX649013
RefSeq transcript (Entrez)NM_001099684 NM_001321178 NM_001321179 NM_001321180 NM_001321181 NM_001321182 NM_001321183 NM_001321186 NM_001321187 NM_001321188
Consensus coding sequences : CCDS (NCBI)FAM156B
Gene ExpressionFAM156B [ NCBI-GEO ]   FAM156B [ EBI - ARRAY_EXPRESS ]   FAM156B [ SEEK ]   FAM156B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM156B [ Firebrowse - Broad ]
GenevisibleExpression of FAM156B in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)727866
GTEX Portal (Tissue expression)FAM156B
Human Protein AtlasENSG00000179304-FAM156B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM156B
Human Protein Atlas [tissue]ENSG00000179304-FAM156B [tissue]
Protein Interaction databases
BioGRIDFAM156B
STRING (EMBL)FAM156B
ZODIACFAM156B
Ontologies - Pathways
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXFAM156B
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 Oct 4 15:49:34 CEST 2021

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.