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FAM170B (family with sequence similarity 170 member B)

Identity

Alias_namesC10orf73
chromosome 10 open reading frame 73
family with sequence similarity 170, member B
Alias_symbol (synonym)Em:AC084727.4
Other alias
HGNC (Hugo) FAM170B
LocusID (NCBI) 170370
Atlas_Id 63067
Location 10q11.23  [Link to chromosome band 10q11]
Location_base_pair Starts at 49131156 and ends at 49134020 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)FAM170B   19736
Cards
Entrez_Gene (NCBI)FAM170B  170370  family with sequence similarity 170 member B
AliasesC10orf73
GeneCards (Weizmann)FAM170B
Ensembl hg19 (Hinxton)ENSG00000172538 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000172538 [Gene_View]  chr10:49131156-49134020 [Contig_View]  FAM170B [Vega]
ICGC DataPortalENSG00000172538
TCGA cBioPortalFAM170B
AceView (NCBI)FAM170B
Genatlas (Paris)FAM170B
WikiGenes170370
SOURCE (Princeton)FAM170B
Genetics Home Reference (NIH)FAM170B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM170B  -     chr10:49131156-49134020 -  10q11.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM170B  -     10q11.23   [Description]    (hg19-Feb_2009)
EnsemblFAM170B - 10q11.23 [CytoView hg19]  FAM170B - 10q11.23 [CytoView hg38]
Mapping of homologs : NCBIFAM170B [Mapview hg19]  FAM170B [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC029839 BC047597
RefSeq transcript (Entrez)NM_001164484
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM170B
Cluster EST : UnigeneHs.646291 [ NCBI ]
CGAP (NCI)Hs.646291
Alternative Splicing GalleryENSG00000172538
Gene ExpressionFAM170B [ NCBI-GEO ]   FAM170B [ EBI - ARRAY_EXPRESS ]   FAM170B [ SEEK ]   FAM170B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM170B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)170370
GTEX Portal (Tissue expression)FAM170B
Protein : pattern, domain, 3D structure
UniProt/SwissProtA6NMN3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA6NMN3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA6NMN3
Splice isoforms : SwissVarA6NMN3
PhosPhoSitePlusA6NMN3
Domains : Interpro (EBI)FAM170B   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM170B
DMDM Disease mutations170370
Blocks (Seattle)FAM170B
SuperfamilyA6NMN3
Human Protein AtlasENSG00000172538
Peptide AtlasA6NMN3
IPIIPI00329168   
Protein Interaction databases
DIP (DOE-UCLA)A6NMN3
IntAct (EBI)A6NMN3
FunCoupENSG00000172538
BioGRIDFAM170B
STRING (EMBL)FAM170B
ZODIACFAM170B
Ontologies - Pathways
QuickGOA6NMN3
Ontology : AmiGOacrosomal vesicle  outer acrosomal membrane  protein binding  regulation of fertilization  positive regulation of acrosome reaction  
Ontology : EGO-EBIacrosomal vesicle  outer acrosomal membrane  protein binding  regulation of fertilization  positive regulation of acrosome reaction  
NDEx NetworkFAM170B
Atlas of Cancer Signalling NetworkFAM170B
Wikipedia pathwaysFAM170B
Orthology - Evolution
OrthoDB170370
GeneTree (enSembl)ENSG00000172538
Phylogenetic Trees/Animal Genes : TreeFamFAM170B
HOVERGENA6NMN3
HOGENOMA6NMN3
Homologs : HomoloGeneFAM170B
Homology/Alignments : Family Browser (UCSC)FAM170B
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM170B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM170B
dbVarFAM170B
ClinVarFAM170B
1000_GenomesFAM170B 
Exome Variant ServerFAM170B
ExAC (Exome Aggregation Consortium)FAM170B (select the gene name)
Genetic variants : HAPMAP170370
Genomic Variants (DGV)FAM170B [DGVbeta]
DECIPHERFAM170B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM170B 
Mutations
ICGC Data PortalFAM170B 
TCGA Data PortalFAM170B 
Broad Tumor PortalFAM170B
OASIS PortalFAM170B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAM170B  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFAM170B
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 FAM170B
DgiDB (Drug Gene Interaction Database)FAM170B
DoCM (Curated mutations)FAM170B (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM170B (select a term)
intoGenFAM170B
Cancer3DFAM170B(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM170B
Genetic Testing Registry FAM170B
NextProtA6NMN3 [Medical]
TSGene170370
GENETestsFAM170B
Target ValidationFAM170B
Huge Navigator FAM170B [HugePedia]
snp3D : Map Gene to Disease170370
BioCentury BCIQFAM170B
ClinGenFAM170B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD170370
Chemical/Pharm GKB GenePA162387168
Clinical trialFAM170B
Miscellaneous
canSAR (ICR)FAM170B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM170B
EVEXFAM170B
GoPubMedFAM170B
iHOPFAM170B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:07:41 CEST 2017

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