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FAM135B (family with sequence similarity 135 member B)

Identity

Alias_namesfamily with sequence similarity 135, member B
Alias_symbol (synonym)C8ORFK32
Other alias
HGNC (Hugo) FAM135B
LocusID (NCBI) 51059
Atlas_Id 63025
Location 8q24.23  [Link to chromosome band 8q24]
Location_base_pair Starts at 138130023 and ends at 138496822 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)FAM135B   28029
Cards
Entrez_Gene (NCBI)FAM135B  51059  family with sequence similarity 135 member B
AliasesC8ORFK32
GeneCards (Weizmann)FAM135B
Ensembl hg19 (Hinxton)ENSG00000147724 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000147724 [Gene_View]  chr8:138130023-138496822 [Contig_View]  FAM135B [Vega]
ICGC DataPortalENSG00000147724
TCGA cBioPortalFAM135B
AceView (NCBI)FAM135B
Genatlas (Paris)FAM135B
WikiGenes51059
SOURCE (Princeton)FAM135B
Genetics Home Reference (NIH)FAM135B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM135B  -     chr8:138130023-138496822 -  8q24.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM135B  -     8q24.23   [Description]    (hg19-Feb_2009)
EnsemblFAM135B - 8q24.23 [CytoView hg19]  FAM135B - 8q24.23 [CytoView hg38]
Mapping of homologs : NCBIFAM135B [Mapview hg19]  FAM135B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB196635 AF131744 AK091433 BC037288 BC038357
RefSeq transcript (Entrez)NM_015912
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM135B
Cluster EST : UnigeneHs.662285 [ NCBI ]
CGAP (NCI)Hs.662285
Alternative Splicing GalleryENSG00000147724
Gene ExpressionFAM135B [ NCBI-GEO ]   FAM135B [ EBI - ARRAY_EXPRESS ]   FAM135B [ SEEK ]   FAM135B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM135B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)51059
GTEX Portal (Tissue expression)FAM135B
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ49AJ0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ49AJ0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ49AJ0
Splice isoforms : SwissVarQ49AJ0
PhosPhoSitePlusQ49AJ0
Domains : Interpro (EBI)AB_hydrolase    DUF3657    DUF676_lipase-like   
Domain families : Pfam (Sanger)DUF3657 (PF12394)    DUF676 (PF05057)   
Domain families : Pfam (NCBI)pfam12394    pfam05057   
Conserved Domain (NCBI)FAM135B
DMDM Disease mutations51059
Blocks (Seattle)FAM135B
SuperfamilyQ49AJ0
Human Protein AtlasENSG00000147724
Peptide AtlasQ49AJ0
HPRD14230
IPIIPI00852662   IPI00877691   IPI00658160   IPI00878074   IPI00974569   IPI00980580   IPI00973180   IPI00974415   
Protein Interaction databases
DIP (DOE-UCLA)Q49AJ0
IntAct (EBI)Q49AJ0
FunCoupENSG00000147724
BioGRIDFAM135B
STRING (EMBL)FAM135B
ZODIACFAM135B
Ontologies - Pathways
QuickGOQ49AJ0
Ontology : AmiGOcellular lipid metabolic process  carboxylic ester hydrolase activity  
Ontology : EGO-EBIcellular lipid metabolic process  carboxylic ester hydrolase activity  
NDEx NetworkFAM135B
Atlas of Cancer Signalling NetworkFAM135B
Wikipedia pathwaysFAM135B
Orthology - Evolution
OrthoDB51059
GeneTree (enSembl)ENSG00000147724
Phylogenetic Trees/Animal Genes : TreeFamFAM135B
HOVERGENQ49AJ0
HOGENOMQ49AJ0
Homologs : HomoloGeneFAM135B
Homology/Alignments : Family Browser (UCSC)FAM135B
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM135B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM135B
dbVarFAM135B
ClinVarFAM135B
1000_GenomesFAM135B 
Exome Variant ServerFAM135B
ExAC (Exome Aggregation Consortium)FAM135B (select the gene name)
Genetic variants : HAPMAP51059
Genomic Variants (DGV)FAM135B [DGVbeta]
DECIPHERFAM135B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM135B 
Mutations
ICGC Data PortalFAM135B 
TCGA Data PortalFAM135B 
Broad Tumor PortalFAM135B
OASIS PortalFAM135B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAM135B  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFAM135B
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 FAM135B
DgiDB (Drug Gene Interaction Database)FAM135B
DoCM (Curated mutations)FAM135B (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM135B (select a term)
intoGenFAM135B
Cancer3DFAM135B(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM135B
Genetic Testing Registry FAM135B
NextProtQ49AJ0 [Medical]
TSGene51059
GENETestsFAM135B
Target ValidationFAM135B
Huge Navigator FAM135B [HugePedia]
snp3D : Map Gene to Disease51059
BioCentury BCIQFAM135B
ClinGenFAM135B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD51059
Chemical/Pharm GKB GenePA162386277
Clinical trialFAM135B
Miscellaneous
canSAR (ICR)FAM135B (select the gene name)
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM135B
EVEXFAM135B
GoPubMedFAM135B
iHOPFAM135B
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 15:47:50 CEST 2017

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