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FAM182B (family with sequence similarity 182 member B)

Identity

Alias_namesfamily with sequence similarity 182, member B
Other alias-
HGNC (Hugo) FAM182B
LocusID (NCBI) 728882
Atlas_Id 63088
Location 20p11.1  [Link to chromosome band 20p11]
Location_base_pair Starts at 25769598 and ends at 25801291 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)FAM182B   34503
Cards
Entrez_Gene (NCBI)FAM182B  728882  family with sequence similarity 182 member B
Aliases
GeneCards (Weizmann)FAM182B
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr20:25769598-25801291 [Contig_View]  FAM182B [Vega]
TCGA cBioPortalFAM182B
AceView (NCBI)FAM182B
Genatlas (Paris)FAM182B
WikiGenes728882
SOURCE (Princeton)FAM182B
Genetics Home Reference (NIH)FAM182B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM182B  -     chr20:25769598-25801291 -  20p11.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM182B  -     20p11.1   [Description]    (hg19-Feb_2009)
EnsemblFAM182B - 20p11.1 [CytoView hg19]  FAM182B - 20p11.1 [CytoView hg38]
Mapping of homologs : NCBIFAM182B [Mapview hg19]  FAM182B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK054844 AL096727 BC042812
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM182B
Cluster EST : UnigeneHs.682103 [ NCBI ]
CGAP (NCI)Hs.682103
Gene ExpressionFAM182B [ NCBI-GEO ]   FAM182B [ EBI - ARRAY_EXPRESS ]   FAM182B [ SEEK ]   FAM182B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM182B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)728882
GTEX Portal (Tissue expression)FAM182B
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5T319   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5T319  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5T319
Splice isoforms : SwissVarQ5T319
PhosPhoSitePlusQ5T319
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM182B
DMDM Disease mutations728882
Blocks (Seattle)FAM182B
SuperfamilyQ5T319
Peptide AtlasQ5T319
IPIIPI00880155   IPI00900344   
Protein Interaction databases
DIP (DOE-UCLA)Q5T319
IntAct (EBI)Q5T319
BioGRIDFAM182B
STRING (EMBL)FAM182B
ZODIACFAM182B
Ontologies - Pathways
QuickGOQ5T319
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkFAM182B
Atlas of Cancer Signalling NetworkFAM182B
Wikipedia pathwaysFAM182B
Orthology - Evolution
OrthoDB728882
Phylogenetic Trees/Animal Genes : TreeFamFAM182B
HOVERGENQ5T319
HOGENOMQ5T319
Homologs : HomoloGeneFAM182B
Homology/Alignments : Family Browser (UCSC)FAM182B
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM182B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM182B
dbVarFAM182B
ClinVarFAM182B
1000_GenomesFAM182B 
Exome Variant ServerFAM182B
ExAC (Exome Aggregation Consortium)FAM182B (select the gene name)
Genetic variants : HAPMAP728882
Genomic Variants (DGV)FAM182B [DGVbeta]
DECIPHERFAM182B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM182B 
Mutations
ICGC Data PortalFAM182B 
TCGA Data PortalFAM182B 
Broad Tumor PortalFAM182B
OASIS PortalFAM182B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAM182B  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFAM182B
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 FAM182B
DgiDB (Drug Gene Interaction Database)FAM182B
DoCM (Curated mutations)FAM182B (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM182B (select a term)
intoGenFAM182B
Cancer3DFAM182B(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM182B
Genetic Testing Registry FAM182B
NextProtQ5T319 [Medical]
TSGene728882
GENETestsFAM182B
Target ValidationFAM182B
Huge Navigator FAM182B [HugePedia]
snp3D : Map Gene to Disease728882
BioCentury BCIQFAM182B
ClinGenFAM182B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD728882
Chemical/Pharm GKB GenePA162387614
Clinical trialFAM182B
Miscellaneous
canSAR (ICR)FAM182B (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM182B
EVEXFAM182B
GoPubMedFAM182B
iHOPFAM182B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 15:48:03 CEST 2017

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