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FAM151B (family with sequence similarity 151 member B)

Identity

Alias_namesfamily with sequence similarity 151
Alias_symbol (synonym)UNQ9217
Other alias
HGNC (Hugo) FAM151B
LocusID (NCBI) 167555
Atlas_Id 54301
Location 5q14.1  [Link to chromosome band 5q14]
Location_base_pair Starts at 79783800 and ends at 79838382 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
FAM151B (5q14.1) / CASP12 (11q22.3)

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

 


Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 1 ]
  Lung: Translocations in Squamous Cell Carcinoma


External links

Nomenclature
HGNC (Hugo)FAM151B   33716
Cards
Entrez_Gene (NCBI)FAM151B  167555  family with sequence similarity 151 member B
AliasesUNQ9217
GeneCards (Weizmann)FAM151B
Ensembl hg19 (Hinxton)ENSG00000152380 [Gene_View]  chr5:79783800-79838382 [Contig_View]  FAM151B [Vega]
Ensembl hg38 (Hinxton)ENSG00000152380 [Gene_View]  chr5:79783800-79838382 [Contig_View]  FAM151B [Vega]
ICGC DataPortalENSG00000152380
TCGA cBioPortalFAM151B
AceView (NCBI)FAM151B
Genatlas (Paris)FAM151B
WikiGenes167555
SOURCE (Princeton)FAM151B
Genetics Home Reference (NIH)FAM151B
Genomic and cartography
GoldenPath hg19 (UCSC)FAM151B  -     chr5:79783800-79838382 +  5q14.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)FAM151B  -     5q14.1   [Description]    (hg38-Dec_2013)
EnsemblFAM151B - 5q14.1 [CytoView hg19]  FAM151B - 5q14.1 [CytoView hg38]
Mapping of homologs : NCBIFAM151B [Mapview hg19]  FAM151B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AY358256 BC131563 BC142990 T10044
RefSeq transcript (Entrez)NM_205548
RefSeq genomic (Entrez)NC_000005 NC_018916 NT_034772 NW_004929322
Consensus coding sequences : CCDS (NCBI)FAM151B
Cluster EST : UnigeneHs.592674 [ NCBI ]
CGAP (NCI)Hs.592674
Alternative Splicing GalleryENSG00000152380
Gene ExpressionFAM151B [ NCBI-GEO ]   FAM151B [ EBI - ARRAY_EXPRESS ]   FAM151B [ SEEK ]   FAM151B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM151B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)167555
GTEX Portal (Tissue expression)FAM151B
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6UXP7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6UXP7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6UXP7
Splice isoforms : SwissVarQ6UXP7
PhosPhoSitePlusQ6UXP7
Domains : Interpro (EBI)DUF2181   
Domain families : Pfam (Sanger)DUF2181 (PF10223)   
Domain families : Pfam (NCBI)pfam10223   
Conserved Domain (NCBI)FAM151B
DMDM Disease mutations167555
Blocks (Seattle)FAM151B
SuperfamilyQ6UXP7
Human Protein AtlasENSG00000152380
Peptide AtlasQ6UXP7
HPRD18272
IPIIPI00409634   IPI00966627   
Protein Interaction databases
DIP (DOE-UCLA)Q6UXP7
IntAct (EBI)Q6UXP7
FunCoupENSG00000152380
BioGRIDFAM151B
STRING (EMBL)FAM151B
ZODIACFAM151B
Ontologies - Pathways
QuickGOQ6UXP7
Ontology : AmiGOprotein binding  
Ontology : EGO-EBIprotein binding  
NDEx NetworkFAM151B
Atlas of Cancer Signalling NetworkFAM151B
Wikipedia pathwaysFAM151B
Orthology - Evolution
OrthoDB167555
GeneTree (enSembl)ENSG00000152380
Phylogenetic Trees/Animal Genes : TreeFamFAM151B
HOVERGENQ6UXP7
HOGENOMQ6UXP7
Homologs : HomoloGeneFAM151B
Homology/Alignments : Family Browser (UCSC)FAM151B
Gene fusions - Rearrangements
Fusion : MitelmanFAM151B/CASP12 [5q14.1/11q22.3]  
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM151B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM151B
dbVarFAM151B
ClinVarFAM151B
1000_GenomesFAM151B 
Exome Variant ServerFAM151B
ExAC (Exome Aggregation Consortium)FAM151B (select the gene name)
Genetic variants : HAPMAP167555
Genomic Variants (DGV)FAM151B [DGVbeta]
DECIPHER (Syndromes)5:79783800-79838382  ENSG00000152380
CONAN: Copy Number AnalysisFAM151B 
Mutations
ICGC Data PortalFAM151B 
TCGA Data PortalFAM151B 
Broad Tumor PortalFAM151B
OASIS PortalFAM151B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAM151B  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFAM151B
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch FAM151B
DgiDB (Drug Gene Interaction Database)FAM151B
DoCM (Curated mutations)FAM151B (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM151B (select a term)
intoGenFAM151B
Cancer3DFAM151B(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM151B
Genetic Testing Registry FAM151B
NextProtQ6UXP7 [Medical]
TSGene167555
GENETestsFAM151B
Huge Navigator FAM151B [HugePedia]
snp3D : Map Gene to Disease167555
BioCentury BCIQFAM151B
ClinGenFAM151B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD167555
Chemical/Pharm GKB GenePA162386486
Clinical trialFAM151B
Miscellaneous
canSAR (ICR)FAM151B (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM151B
EVEXFAM151B
GoPubMedFAM151B
iHOPFAM151B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 13:05:24 CET 2017

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