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FAM234B (family with sequence similarity 234 member B)

Identity

Alias_namesKIAA1467
KIAA1467
family with sequence similarity 234, member B
Other alias
HGNC (Hugo) FAM234B
LocusID (NCBI) 57613
Atlas_Id 77725
Location 12p13.1  [Link to chromosome band 12p13]
Location_base_pair Starts at 13044381 and ends at 13083449 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
FAM234B (12p13.1) / GPRC5A (12p13.1)FAM234B (12p13.1) / MALAT1 (11q13.1)LYRM2 (6q15) / FAM234B (12p13.1)
PPM1H (12q14.1) / FAM234B (12p13.1)

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)FAM234B   29288
Cards
Entrez_Gene (NCBI)FAM234B  57613  family with sequence similarity 234 member B
AliasesKIAA1467
GeneCards (Weizmann)FAM234B
Ensembl hg19 (Hinxton)ENSG00000084444 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000084444 [Gene_View]  chr12:13044381-13083449 [Contig_View]  FAM234B [Vega]
ICGC DataPortalENSG00000084444
TCGA cBioPortalFAM234B
AceView (NCBI)FAM234B
Genatlas (Paris)FAM234B
WikiGenes57613
SOURCE (Princeton)FAM234B
Genetics Home Reference (NIH)FAM234B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM234B  -     chr12:13044381-13083449 +  12p13.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM234B  -     12p13.1   [Description]    (hg19-Feb_2009)
EnsemblFAM234B - 12p13.1 [CytoView hg19]  FAM234B - 12p13.1 [CytoView hg38]
Mapping of homologs : NCBIFAM234B [Mapview hg19]  FAM234B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB040900 AK125278 AK125676 AK294732 AL832902
RefSeq transcript (Entrez)NM_020853
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM234B
Cluster EST : UnigeneHs.712857 [ NCBI ]
CGAP (NCI)Hs.712857
Alternative Splicing GalleryENSG00000084444
Gene ExpressionFAM234B [ NCBI-GEO ]   FAM234B [ EBI - ARRAY_EXPRESS ]   FAM234B [ SEEK ]   FAM234B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM234B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57613
GTEX Portal (Tissue expression)FAM234B
Protein : pattern, domain, 3D structure
UniProt/SwissProtA2RU67   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA2RU67  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA2RU67
Splice isoforms : SwissVarA2RU67
PhosPhoSitePlusA2RU67
Domains : Interpro (EBI)Quinoprotein_ADH-like_fam    Quinoprotein_ADH-like_supfam   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM234B
DMDM Disease mutations57613
Blocks (Seattle)FAM234B
SuperfamilyA2RU67
Human Protein AtlasENSG00000084444
Peptide AtlasA2RU67
HPRD11149
IPIIPI00375879   IPI00909946   IPI00790497   
Protein Interaction databases
DIP (DOE-UCLA)A2RU67
IntAct (EBI)A2RU67
FunCoupENSG00000084444
BioGRIDFAM234B
STRING (EMBL)FAM234B
ZODIACFAM234B
Ontologies - Pathways
QuickGOA2RU67
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkFAM234B
Atlas of Cancer Signalling NetworkFAM234B
Wikipedia pathwaysFAM234B
Orthology - Evolution
OrthoDB57613
GeneTree (enSembl)ENSG00000084444
Phylogenetic Trees/Animal Genes : TreeFamFAM234B
HOVERGENA2RU67
HOGENOMA2RU67
Homologs : HomoloGeneFAM234B
Homology/Alignments : Family Browser (UCSC)FAM234B
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM234B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM234B
dbVarFAM234B
ClinVarFAM234B
1000_GenomesFAM234B 
Exome Variant ServerFAM234B
ExAC (Exome Aggregation Consortium)FAM234B (select the gene name)
Genetic variants : HAPMAP57613
Genomic Variants (DGV)FAM234B [DGVbeta]
DECIPHERFAM234B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM234B 
Mutations
ICGC Data PortalFAM234B 
TCGA Data PortalFAM234B 
Broad Tumor PortalFAM234B
OASIS PortalFAM234B [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDFAM234B
BioMutasearch FAM234B
DgiDB (Drug Gene Interaction Database)FAM234B
DoCM (Curated mutations)FAM234B (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM234B (select a term)
intoGenFAM234B
Cancer3DFAM234B(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM234B
Genetic Testing Registry FAM234B
NextProtA2RU67 [Medical]
TSGene57613
GENETestsFAM234B
Target ValidationFAM234B
Huge Navigator FAM234B [HugePedia]
snp3D : Map Gene to Disease57613
BioCentury BCIQFAM234B
ClinGenFAM234B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD57613
Chemical/Pharm GKB GenePA128395790
Clinical trialFAM234B
Miscellaneous
canSAR (ICR)FAM234B (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM234B
EVEXFAM234B
GoPubMedFAM234B
iHOPFAM234B
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 15:48:26 CEST 2017

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