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

FAM184B (family with sequence similarity 184 member B)

Identity

Alias_namesfamily with sequence similarity 184, member B
Alias_symbol (synonym)KIAA1276
Other alias-
HGNC (Hugo) FAM184B
LocusID (NCBI) 27146
Atlas_Id 63092
Location 4p15.32  [Link to chromosome band 4p15]
Location_base_pair Starts at 17632086 and ends at 17781512 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
FAM184B (4p15.32) / ABL1 (9q34.12)

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)FAM184B   29235
Cards
Entrez_Gene (NCBI)FAM184B  27146  family with sequence similarity 184 member B
Aliases
GeneCards (Weizmann)FAM184B
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr4:17632086-17781512 [Contig_View]  FAM184B [Vega]
TCGA cBioPortalFAM184B
AceView (NCBI)FAM184B
Genatlas (Paris)FAM184B
WikiGenes27146
SOURCE (Princeton)FAM184B
Genetics Home Reference (NIH)FAM184B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM184B  -     chr4:17632086-17781512 -  4p15.32   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM184B  -     4p15.32   [Description]    (hg19-Feb_2009)
EnsemblFAM184B - 4p15.32 [CytoView hg19]  FAM184B - 4p15.32 [CytoView hg38]
Mapping of homologs : NCBIFAM184B [Mapview hg19]  FAM184B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB033102 AK027311 AK308144
RefSeq transcript (Entrez)NM_015688
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM184B
Cluster EST : UnigeneHs.744951 [ NCBI ]
CGAP (NCI)Hs.744951
Gene ExpressionFAM184B [ NCBI-GEO ]   FAM184B [ EBI - ARRAY_EXPRESS ]   FAM184B [ SEEK ]   FAM184B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM184B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)27146
GTEX Portal (Tissue expression)FAM184B
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9ULE4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9ULE4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9ULE4
Splice isoforms : SwissVarQ9ULE4
PhosPhoSitePlusQ9ULE4
Domains : Interpro (EBI)FAM184    FAM184B   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM184B
DMDM Disease mutations27146
Blocks (Seattle)FAM184B
SuperfamilyQ9ULE4
Peptide AtlasQ9ULE4
IPIIPI00297208   
Protein Interaction databases
DIP (DOE-UCLA)Q9ULE4
IntAct (EBI)Q9ULE4
BioGRIDFAM184B
STRING (EMBL)FAM184B
ZODIACFAM184B
Ontologies - Pathways
QuickGOQ9ULE4
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkFAM184B
Atlas of Cancer Signalling NetworkFAM184B
Wikipedia pathwaysFAM184B
Orthology - Evolution
OrthoDB27146
Phylogenetic Trees/Animal Genes : TreeFamFAM184B
HOVERGENQ9ULE4
HOGENOMQ9ULE4
Homologs : HomoloGeneFAM184B
Homology/Alignments : Family Browser (UCSC)FAM184B
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM184B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM184B
dbVarFAM184B
ClinVarFAM184B
1000_GenomesFAM184B 
Exome Variant ServerFAM184B
ExAC (Exome Aggregation Consortium)FAM184B (select the gene name)
Genetic variants : HAPMAP27146
Genomic Variants (DGV)FAM184B [DGVbeta]
DECIPHERFAM184B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM184B 
Mutations
ICGC Data PortalFAM184B 
TCGA Data PortalFAM184B 
Broad Tumor PortalFAM184B
OASIS PortalFAM184B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAM184B  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFAM184B
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 FAM184B
DgiDB (Drug Gene Interaction Database)FAM184B
DoCM (Curated mutations)FAM184B (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM184B (select a term)
intoGenFAM184B
Cancer3DFAM184B(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM184B
Genetic Testing Registry FAM184B
NextProtQ9ULE4 [Medical]
TSGene27146
GENETestsFAM184B
Huge Navigator FAM184B [HugePedia]
snp3D : Map Gene to Disease27146
BioCentury BCIQFAM184B
ClinGenFAM184B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD27146
Chemical/Pharm GKB GenePA164719809
Clinical trialFAM184B
Miscellaneous
canSAR (ICR)FAM184B (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM184B
EVEXFAM184B
GoPubMedFAM184B
iHOPFAM184B
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 : Fri May 19 11:10:52 CEST 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.